FDA Recall
🇺🇸 United States
TerminatedTerminated: September 18, 20262026 recordClass I
Ron's Home Style Foods, Inc.
- Product
- Item #DIPSAU0205RFS Salsa Autentica 5 lb. packaged in round…
- Reason
- Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella
- Published
- September 9, 2026
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: September 18, 20262026 recordClass I
Ron's Home Style Foods, Inc.
- Product
- Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round pl…
- Reason
- Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella
- Published
- September 9, 2026
- Distribution
- Multiple states
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USDA FSIS Recall
🇺🇸 United States
Status not reported2026 record
El Eden Import Distributor Corp Recalls Ineligible Pork Cracklings Products Imported from The Republic of Colombia
- Reason
- <img align="left" hspace="5" src="https://www.fsis.usda.gov/sites/default/files/2023-04/Icon-Recalls.png"/> Editor's Note: This release was updated on September 17, 2026, to add additional states, including Massachusetts, New York, Connecticut, and Illinois, and to remove the specific July 28 import date...
- Published
- September 9, 2026
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FDA Recall
🇺🇸 United States
Status not reported2026 record
FreshPoint Issues Recall Due to an Improperly Declared Allergen (Egg) in Chicken Salad Wedge Sandwiches
- Reason
- September 4, 2026 Orlando, FL– FreshPoint of Orlando, FL., is issuing a voluntary recall of 1,093 units of specific lots of Cranberry Chicken Salad Wedge sandwiches due to an improperly declared allergen (eggs). People who have an allergy or severe sensitivity to eggs run the risk of serious or lif
- Published
- September 8, 2026
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USDA FSIS Recall
🇺🇸 United States
Status not reported2026 record
Prime Line Distributors, Inc. and Ferrarini USA, Inc. Recall Imported Ready-To-Eat Pork Guanciale Products Due to Possible Listeria Contamination
- Reason
- <img align="left" hspace="5" src="https://www.fsis.usda.gov/sites/default/files/2023-04/Icon-Recalls.png"/> WASHINGTON, Sept. 06, 2026 - Prime Line Distributors, Inc., a Fort Lauderdale, Fla., firm, and Ferrarini USA, Inc., a Hoboken, N.J., firm, are recalling approximately 1,513 pounds of imported ready-to-eat...
- Published
- September 6, 2026
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FDA Recall
🇺🇸 United States
Status not reported2026 record
Made Fresh Salads, Inc. Recalls Ready to Eat Deli Style Salads and Cream Cheese Because of Possible Health Risk
- Reason
- Made Fresh Salads Inc. of Bay Shore, NY is recalling all Ready to Eat Deli Style Salads and cream cheese, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and
- Published
- September 6, 2026
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FDA Recall
🇺🇸 United States
Status not reported2026 record
Foods Alive Recalls Organic Moringa Leaf Powder Because of Possible Health Risk
- Reason
- Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have 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
- Published
- September 4, 2026
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FDA Recall
🇺🇸 United States
Status not reported2026 record
SUPPLX.com Issues Voluntary Nationwide Recall of Business Pill and Branch Manager for Men Due to Undeclared Yohimbine
- Reason
- Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.
- Published
- September 3, 2026
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FDA Recall
🇺🇸 United States
Status not reported2026 record
American Regent, Inc. Issues Voluntary Nationwide Recall of Three Lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) Due to the Presence of Particulate Matter and Lack of Assurance of Sterility
- Reason
- FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, re
- Published
- September 3, 2026
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FDA Recall
🇺🇸 United States
Ongoing2026 recordClass II
Africando Foods LLC
- Product
- Clear glass bottle with black screw lid with multi label whi…
- Reason
- Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list
- Published
- September 2, 2026
- Distribution
- 8 wholesale and retail locations in IA,…
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FDA Recall
🇺🇸 United States
Ongoing2026 recordClass II
Horizon Organic Dairy, LLC
- Product
- Horizon Organic ORG ASEP CHOC MILK 1% 8OZ 12 CT (Item 136990…
- Reason
- Product has the potential to be spoiled.
- Published
- September 2, 2026
- Distribution
- Distributed throughout the United States…
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FDA Recall
Ongoing2026 recordClass I
Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00
by B BRAUN MEDICAL INC
- Reason
- Presence of Particulate matter.
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass II
Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bottles, Rx only, Manufactured for: Exelan Pharmaceuticals, Inc., Boca Raton, FL 33432, Manufactured by: West-Ward Columbus Inc., Columbus, OH 43228.
by Hikma Pharmaceuticals USA Inc.
- Reason
- Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass I
Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, Illinois, 60047, NDC 65219-594-20.
by Fresenius Kabi USA, LLC
- Reason
- Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass II
Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-4379-3
by Apotex Corp.
- Reason
- Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass II
Acthar Gel (repository corticotropin injection), 5 mL multiple-dose vial, Rx Only, Mfd. for: Mallinckrodt ARD LLC, Bridgewater, NJ 08807, NDC 63004-8710-1 & NDC 63004-8710-2
by Mallinckrodt Hospital Products Inc.
- Reason
- Presence of particulate matter: glass and stopper piece
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass II
Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205.
by Church & Dwight Co., Inc.
- Reason
- CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass II
Clobetasol Propionate Cream USP, 0.05%, 60 g tube, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, United States, Manufactured by: Lupin Limited, Pithampur (MP) 454 775, INDIA, NDC 68180-956-04.
by Lupin Pharmaceuticals Inc.
- Reason
- Failed content uniformity specifications.
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass II
Levothyroxine Sodium Tablets, USP, 300 mcg (0.3 mg), 90-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-458-15.
by ACCORD HEALTHCARE, INC.
- Reason
- Subpotent Drug
- Published
- September 2, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing2026 recordClass II
Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg), packaged in a) 90-count bottles (NDC 16729-457-15) and b) 1000-count bottles (NDC 16729-457-17), Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India.
by ACCORD HEALTHCARE, INC.
- Reason
- Subpotent Drug
- Published
- September 2, 2026
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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