Recalls
On this page you’ll find recent recall alerts for food and feed products distributed or produced in Georgia. These alerts include the reason for the recall, a description of the issue, and a complete listing of affected products with identifying information.
Learn more about recallsColonna Brothers, Inc. (03/06/2024)
Colonna Brothers of North Bergen, NJ is recalling its 1.5oz Marcum Ground Cinnamon & 2.25oz Supreme Tradition Ground Cinnamon because of a possible health risk due to elevated lead levels. Short term exposures to very low levels of lead may not elicit any symptoms. It is possible that increased blood lead levels may be the only apparent sign of lead exposure. Additional signs and symptoms of lead exposure are more likely with acute exposure to higher levels of lead or chronic exposure to lead. The effects depend upon the amount and duration of lead exposure and age/ body weight. If a child is exposed to enough lead for a protracted period of time (e.g., weeks to months) permanent damage to the central nervous system may occur. This can result in learning disorders, developmental defects, and other long-term health problems. For adults, chronic lead exposure is associated with kidney dysfunction, hypertension, and neurocognitive effects.
The Cinnamon was distributed nationwide through retail stores and mail order. The products come in a clear plastic jar labeled with either “Marcum Cinnamon Ground 1.5oz” or “Supreme Tradition Ground Cinnamon 2.25oz”. Only the following lot codes (found on the jar above the label - below the cap) were affected:
| 1.5oz Marcum Ground Cinnamon | Best By:10/16/25 10DB |
| 1.5oz Marcum Ground Cinnamon | Best By: 04/06/25 0400B1 |
| 2.25oz Supreme Tradition Ground Cinnamon | 09/29/25 09E8 |
| 2.25oz Supreme Tradition Ground Cinnamon | 04/17/25 04E11 |
| 2.25oz Supreme Tradition Ground Cinnamon | 12/19/25 12C2 |
| 2.25oz Supreme Tradition Ground Cinnamon | 04/12/25 04ECB12 |
| 2.25oz Supreme Tradition Ground Cinnamon | 08/24/25 08A |
| 2.25oz Supreme Tradition Ground Cinnamon | 04/21/25 04E5 |
| 2.25oz Supreme Tradition Ground Cinnamon | 09/22/2025 09E20 |
Consumers who have purchased the Supreme Tradition Ground Cinnamon or Marcum Ground Cinnamon, with the lot codes listed above, can discard it or return it to the store for a full refund. Anyone concerned they may have been exposed to lead, should contact their healthcare provider to report their symptoms. Consumers with questions may contact us at 201-864-1115 between the hours of 9-5 EST.
Raja Foods LLC (03/06/2024)
Raja Foods LLC of Skokie, Il is recalling its 3.5 ounce package of "SWAD CINNAMON POWDER" because it has the potential to be contaminated with lead. Short term exposure to very low levels of lead may not elicit any symptoms. It is possible that increased blood levels may be the only apparent sign of lead exposure. Additional signs and symptoms of lead exposure are more likely with acute exposures to higher levels of lead or chronic exposure to lead. While lead can affect nearly every bodily system, its effects depend upon the amount and duration of lead exposure and age/body weight. If a child is exposed to lead for a protracted period of time (e.g., weeks to months) permanent damage to the central nervous system may occur. This can result in learning disorders, developmental defects, and other long-term health problems. For adults, chronic lead exposure is associated with kidney dysfunction, hypertension, and neurocognitive effects.
The products included in this recall are, SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, from either of the following two batches and Best Before Dates: Batch KX21223 Best Before July 2026 and Batch KX08123 Best Before March 2026.
Product was distributed thru retail grocery stores in the Midwest, Northeast, and Southeast regions of the United States. There have been no illnesses reported to date. The recall was the result of a routine sampling program by the FDA.
Consumers who have purchased “SWAD CINNAMON POWDER 3.5OZ” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 847.972.2865, Monday to Friday 9am to 4pm CST.
FDA Alert - Cinnamon Products (03/06/2024)
The U.S. Food and Drug Administration is taking several additional steps to address concerns about elevated lead levels in cinnamon following the recent incident associated with certain cinnamon apple sauce pouches that resulted in lead poisoning in young children. Today, the agency sent a letter to all cinnamon manufacturers, processors, distributors and facility operators in the U.S., reminding them of the requirement to implement controls to prevent contamination from potential chemical hazards in food, including ground cinnamon products. The agency is also recommending the voluntary recall of certain ground cinnamon products sold by a number of brands at six different retail chains that were found to contain elevated levels of lead.
The agency notified the distributors and manufacturers of products found to contain elevated levels of lead and recommended that the manufacturers voluntarily recall these products because prolonged exposure to them may be unsafe. The products were identified during an FDA-initiated sampling and testing effort to assess cinnamon sold across numerous retail stores. No illnesses or adverse events have been reported to date related to the ground cinnamon products listed below, but the FDA is concerned that, because of the elevated lead levels in these products, continued and prolonged use of the products may be unsafe.
The FDA is advising consumers to throw away and not to buy the ground cinnamon products with the lot codes listed below because samples of these products were found to contain elevated levels of lead. Consumers can find lot codes listed on the product’s label. The FDA is working with the firms listed below to voluntarily recall the products, with the exception of the MTCI cinnamon. The FDA has been unable to reach MTCI to share its findings and request that the company initiate a recall. The FDA will update its Safety Alert with new information as it becomes available.
| Ground Cinnamon Distributor | Ground Cinnamon Retailer(s) | Ground Cinnamon Lot Code(s) |
|---|---|---|
| La Fiesta Food Products La Miranda, CA |
La Superior SuperMercados | 25033 |
| Marcum, Moran Foods, LLC Saint Ann, MO |
Save A Lot | Best By: 10/16/25 10 DB; 04/06/25 0400B1 |
| MTCI Santa Fe Springs, CA |
SF Supermarket | No codes |
| SWAD, Raja Foods LLC Skokie, IL |
Patel Brothers | KX21223 Best Before: July 2026 |
| Supreme Tradition, Greenbriar International, Inc. Chesapeake, VA |
Dollar Tree Family Dollar |
Best By: 09/29/25 09E8; 04/17/25 04E11; 12/19/25 12C2; 04/12/25 04ECB12; 08/24/25 08A_ _; 04/21/25 04E5; and 2025-09-22 09E20 |
| El Chilar Apopka, FL |
La Joya Morelense, Baltimore, MD | F275EX1026; D300EX1024 |
It is important to note that the lead levels found in the ground cinnamon products listed above are significantly lower than lead levels in cinnamon in the recalled apple sauce pouches removed from the market this past fall. The products currently recommended for recall contain lead levels ranging from 2.03 to 3.4 parts per million (ppm) lead. The levels of lead in the ground cinnamon recommended for recall is approximately 2,000 ppm to nearly 5,000 ppm lower than the levels of lead associated with the cinnamon in recalled apple puree and apple sauce products. Therefore, these ground cinnamon products do not pose the same level of risk to human health as the apple sauce pouches but could be unsafe for prolonged use.
“Today’s actions serve as a signal to industry that more needs to be done to prevent elevated levels of contaminants from entering our food supply,” said Deputy Commissioner for Human Foods Jim Jones. “Food growers, manufacturers, importers and retailers share a responsibility for ensuring the safety of the foods that reach store shelves. The levels of lead we found in some ground cinnamon products are too high and we must do better to protect those most vulnerable to the negative health outcomes of exposure to elevated levels of lead.”
In the letter sent to the cinnamon industry today, the FDA reminds manufacturers, processors, distributors and facility operators to follow the requirements of the rule Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food, including the requirement to consider chemical hazards that may be present in foods when conducting hazard analyses required by this rule. While the agency continues to emphasize the importance of the cinnamon industry’s responsibility to take measures to prevent potential chemical hazards in its products, the letter to industry and recent recalls highlight how the FDA will request the removal of unsafe cinnamon products from the market.
The agency is also working with Centers for Disease Control and Prevention as well as state and local partners to investigate elevated lead and chromium levels in individuals with reported exposure to apple cinnamon fruit puree pouches manufactured in Ecuador and sold in the U.S. under WanaBana, Weis and Schnucks brands. This work led to a voluntary recall of these products in October 2023.
Related Information
- FDA Alert Concerning Certain Cinnamon Products Due to Presence of Elevated Levels of Lead
- A Conversation with FDA on Steps the Agency is Taking to Address Unsafe Levels of Lead found in Cinnamon
- Action Levels for Lead in Food Intended for Babies and Young Children
- FDA Issues Draft Guidance to Industry on Action Levels for Lead in Baby Foods
- Releases Action Plan for Reducing Exposure to Toxic Elements from Foods for Babies, Young Children
- Lead in Food, Foodwares, and Dietary Supplements
CJ Foods Manufacturing Beaumont Corporation (03/02/2024)
CJ Foods Manufacturing Beaumont Corporation, a Beaumont, Calif., establishment, is recalling approximately 61,839 pounds of steamed chicken soup dumpling products that may be contaminated with foreign materials, specifically hard plastic from a permanent marker pen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The steamed chicken soup dumplings were produced on Dec. 7, 2023. The following products are subject to recall [view labels]:
- 6-oz. boxes with plastic trays containing six pieces of “TRADER JOE’S Steamed Chicken Soup Dumplings” with lot codes “03.07.25.C1-1” and “03.07.25.C1-2” printed on the side of the box.
The products subject to recall bear establishment number “P-46009” inside the USDA mark of inspection. These items were shipped to Trader Joe’s retail locations nationwide.
There have been no confirmed reports of adverse reactions or injury due to consumption of these products. Anyone concerned about an injury should contact a healthcare provider.
Consumers with questions about the recall can contact the CJ Foods Manufacturing Beaumont Corporation’s Consumer Experience Department at 800-544-6855. Members of the media with questions can contact CJ Foods Manufacturing Beaumont Corporation's media relations team at 507-537-8550 or questions@schwans.com.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
Nurture Life, Inc. (02/27/2024)
The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for Nurture Life’s Chicken Parm with Super Veggie Spaghetti meal products due to misbranding and an undeclared allergen. The product’s spaghetti component contains egg white, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to egg are aware that this product should not be consumed.
The fully cooked, not shelf-stable chicken meals were produced between Dec. 27, 2023, and Feb. 20, 2024. The following product is subject to the public health alert [view labels]:
- 5.9-oz. tray with sleeve label containing “nurture life KIDS MEALS CHICKEN PARM WITH SUPER VEGGIE SPAGHETTI” with “enjoy by” dates ranging from Jan. 9, 2024, to March 1, 2024.
The chicken meal packaging does not have a USDA mark of inspection. These items were sold online and shipped directly to consumers nationwide.
Members of the media with questions about this public health alert can contact Frank Chen, Chief Marketing Officer, Nurture Life, Inc., at 312-517-1888 or email at fchen@nurturelife.com. Consumers with questions about this public health alert can contact Jennifer Chow, Co-Founder, Nurture Life, Inc., at 312-517-1888 or email at jchow@nurturelife.com.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
Roland Foods, LLC (02/27/2024)
Roland Foods, LLC (“Roland Foods”) of New York, New York is recalling a specific production code of Roland® Tahini (100% Ground Sesame Seeds) 16 oz. because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Roland® Tahini (100% Ground Sesame Seeds) 16 oz. was distributed to many states through retail stores and foodservice outlets. The product was distributed by Roland Foods from September 2023 through January 2024.
This recall ONLY APPLIES to Roland® Tahini (100% Ground Sesame Seeds) 16 oz., Batch Number P024581, Production Code X0419, UPC Number 10041224701509, with a Best By Date of October 19, 2024. The product can be identified by the UPC, found under the barcode on the back of the product, or by the Production Code and Best Buy Date printed in black ink on the label near the top of the bottle.
To date, Roland Foods has received no reports of illness related to the recalled product.
The recall was as the result of a routine sampling program by the Michigan Department of Agriculture and Rural Development, which revealed that the product tested positive for Salmonella. The company has ceased distribution of the product and has initiated an investigation in partnership with the manufacturer as to the root cause of the problem.
Consumers who have purchased Roland® Tahini (100% Ground Sesame Seeds) 16 oz. are urged to discard any affected product. Consumers with questions may contact the company’s Recall Hotline at 800-622-1823. The Recall Hotline will be monitored from 9:00 a.m. EST – 5:00 p.m. EST.
LQNN, Inc. (02/23/2024)
LQNN Inc., of Garden Grove, California, is voluntarily recalling Banh Ba Xa and varieties of Banh Pia because they may contain undeclared egg. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
The affected products are packaged in various colors of foil bags, with the lot number or best by date printed on the front of the bag. The affected Banh Pia products are under the brand Saigon Gourmet, and all affected products are manufactured by Tan Hue Vien. The twelve (12) affected products are:
| # | PLU # |
Item Name | Lot# | Universal Product Code |
|---|---|---|---|---|
| 1 | 1894 | BANH PIA Mung Bean Durian 480g X16 THV 1894 16pack(17oz-ct)/case |
B4.12.23; B6.12.23; B1.11.23; B2.11.23; B3.11.23; A7.11.23; A8.11.23; A9.11.23; A1.11.23; A2.11.23; A3.11.23; A4.11.23; C9.10.23; C10.10.23; C11.10.23; C6.10.23; C7.10.23; C8.10.23; C2.10.23; C3.10.23; C4.10.23; C5.10.23; C1.10.23; B10.10.23; B4.10.23; B5.10.23; B6.10.23; B7.10.23; B8.10.23; B1.10.23; B2.10.23; A10.10.23 |
8 936014 318942 |
| 2 | 1637 | BANH PIA Mung Bean Pumpkin 400g X30 THV 1637 30pack(14oz-ct)/case |
OCT1525 | 8 936014 316375 |
| 3 | 5181 | BANH PIA Taro Durian 400g X30 THV 5181/1479 30pack(14oz-ct)/case |
DEC0925; NOV1325; OCT1325 | 8 936014 311479 |
| 4 | 1897 | FRZ CAKE Ba Xa Lady 260g X20 THV 1897 20pack(4-ct)/case |
DEC2525; | 8 936014 311752 |
| 5 | 1891 | BANH PIA Black Sesame Durian 400g X30 THV 9178/1891 30pack(14oz-ct)/case |
NOV1625; Oct1525; OCT1325; OCT0225 |
8 936014 319178 |
| 6 | 3077 | BANH PIA Classic Mung Bean Durian 16.8oz X20 THV 3077 20pack(16.8oz-ct)/case |
DEC0925; NOV2725; NOV1625; NOV1325; NOV0425; OCT1325; OCT0225 |
8 936014 313077 |
| 7 | 1794 | BANH PIA Mung Bean Durian 275g X24 THV 1794 24pack(275g-ct)/case |
NOV1625; OCT1525 | 8 936014 317945 |
| 8 | 2112 | BANH PIA Mung Bean Durian 400g X30 THV 0595/2112 30pack(14oz-ct)/case |
DEC1525; DEC0925; NOV1625; NOV1325; OCT2525; OCT1325; OCT0225 |
8 936014 310595 |
| 9 | 1934 | BANH PIA Mung Bean Pineapple 400g X30 THV 1934 30pack(14oz-ct)/case |
Dec0825; NOV1625; OCT1525 | 8 936014 319345 |
| 10 | 1918 | BANH PIA Pandan Durian 400g X30 THV 1918 30pack(14oz-ct)/case |
DEC0925; Nov1825; NOV1325; NOV0425; Oct1325; OCT0225 |
8 936014 319185 |
| 11 | 1890 | BANH PIA Red Bean Durian 400g X30 THV 8904/1890 30pack(14oz-ct)/case |
DEC1525 | 8 936014 318904 |
| 12 | 1638 | BANH PIA Liu Sha Pumpkin 480g X20 THV 1638 20pack(12-ct)/case |
DEC2025. | 8 936014 316603 |
The recalled Banh Ba Xa and varieties of Banh Pia were distributed to Canada, and nationwide to Alabama, Arizona, Arkansas, California, Colorado, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Tennessee, Texas, Utah, Virginia, and Washington to wholesalers, markets, retail stores, and on-line websites.
Consumers who have purchased the above Banh Ba Xa and varieties of Banh Pia are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (714) 949-7870 from Monday through Friday, 8:00 a.m. – 5:00 p.m. PST.
Backstage Center (02/23/2024)
Backstage Center is issuing a recall of approximately 280 Bottles of Alipotec Raiz de Tejocote, dietary supplements, that are labeled with the "Alipotec King" sticker. This recall is being initiated because FDA analysis found that the product contains toxic yellow oleander.
Hazard Statement: The recalled product, which contains yellow oleander instead of tejocote, may induce serious neurologic, gastrointestinal, and cardiovascular adverse health effects. Symptoms may be severe or fatal, including nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac dysrhythmia, and others. Immediate medical attention is advised for consumers experiencing such symptoms.
The product was exclusively distributed on Amazon.com since September 15, 2023.
Product Name: Alipotec King, Alipotec Raiz de Tejocote
Container Description: Cylindrical bottle with a green top, white body, and contains approximately 30 granules, weighing a total of 0.35oz.
Lot Codes: 238124
Expiration date:08-2027
Total Distributed: 280 Bottles
There have been no reports of injury or illness, to date.
Consumer Instructions: Consumers should immediately discontinue use of the product. Customers can visit https://alipotecking.com/recall for instructions on how to process the return of the recalled product.
Contact Information: Should you require further assistance or have any concerns, please do not hesitate to contact Ben Nissan at 818-452-0005 or via email at info@alipotecking.com.
Closing Statement: Backstage Center places the utmost importance on the safety and well-being of our consumers. We deeply regret any worry or inconvenience this recall may have caused. Our commitment to resolving this issue promptly and maintaining the highest standards of product safety and quality remains steadfast.
G.A. Mart (H&Natural) (02/23/2024)
G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native to Mexico and Central America.
Risk Statement: Ingestion of yellow oleander can cause neurologic, gastrointestinal and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia and more.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
H&NATURAL TejoRoot and H&NATURAL Brazil Seed were distributed Nationwide to via internet at https://www.handnatural.com, Amazon.com, and Walmart.com.
The recalled dietary supplements can be identified by the H&NATURAL logo and the following descriptions:
- Tejo Root, Raiz de Tejocte, H&Natural, Healthy and Natural, Dietary Supplement, 10g pills, is packaged in a box or bottle, with UPC (196852946921)
- Brazil Seed Pure Natural Semilla de Brasil, H& Natural, Healthy and Natural, 0.167g seeds, packaged in a box or bottle, with UPC (195893047529) (196852820641) (195893698721) (195893236893)(196852134618) (195893336975)
Recalled lots are labeled with the following expiration dates, 3/24 and 5/24.
Consumers with questions regarding this recall can contact G.A. Mart by phone at (928)389-4805 or ag@gamartgroup.com on Monday through Friday from 9 am to 5 pm, MST.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Complete and submit the report Online
- Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Link to Advisory (English Translation)
Link to Advisory (Spanish Translation)
RAW FARM, LLC (02/16/2024)
RAW FARM, LLC has agreed to initiate a recall of certain lots of RAW FARM- brand Raw Cheddar cheese currently within shelf life due to outbreak of E. Coli 0157:H7. FDA is continuing to work with the firm to remove additional product from the market.
Products:
RAW FARM- brand Raw Cheddar blocks and shredded cheese products:
Affected Product: ONLY Cheese block older than batch 20231113-1 and Shred older than 20240116
| Item | Barcode | Product Description | Package Size (oz) | Brand | Batch or Older |
|---|---|---|---|---|---|
| 1075 | 835204000156 | Raw Cheddar Cheese - Pound Block | 16 | RAW FARM | 20231113-1 |
| 1050 | 835204001177 | Raw Cheddar Cheese - Half Pound Block | 8 | RAW FARM | 20231113-1 |
| 1080 | 835204001184 | Raw Cheddar Cheese - Half Pound Shred | 8 | RAW FARM | 20240116 |
- Original Flavor: all sizes of blocks and shredded packages
- Cheddar with added Jalapeño Flavor: all sizes of blocks and shredded packages
Recommendations:
- Do not eat, sell, or serve RAW FARM-brand Raw Cheddar cheese products.
- Check your refrigerators and freezers for the RAW FARM-brand Raw Cheddar cheese (blocks or shredded) and throw them away. If you froze a product without the original packaging and can’t identify the brand, throw it away.
- Consumers, restaurants, and retailers who purchased or received RAW FARM-brand Raw Cheddar cheese, including wholesale products, should carefully clean and sanitize any surfaces or containers that it touched. Follow FDA’s safe handling and cleaning advice to reduce the risk of cross-contamination.
- Retailers that purchased this product and repackaged it for individual sale should remove the product from the market.
- Due to the range in severity of illness, people should consult their health care provider if they suspect that they have developed symptoms that resemble an E. coli infection.