FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Nate's Fine Foods, LLC
- Product
- COOKED FETTUCCINE PASTA 6 X 5 lbs pouches Net Weight: 30 lbs…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Nate's Fine Foods, LLC
- Product
- TAYLOR FARMS COOKED TROTOLLE MAP 8 X 2.75 lb pouches Net Wei…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Nate's Fine Foods, LLC
- Product
- TAYLOR FARMS COOKED ROTINI MAP 8 X 3 lb pouches Net Weight:…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Nate's Fine Foods, LLC
- Product
- COOKED LINGUINE PASTA 5LB POUCHES PERISHABLE KEEP REFRIGERAT…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Nate's Fine Foods, LLC
- Product
- FRESH CREATIVE FOODS COOKED PENNE PASTA 8 x 3 lb pouches Net…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Nate's Fine Foods, LLC
- Product
- MAP COOKED FETTUCCINE PASTA 6 x 5 lbs pouches Net Weight: 30…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Nate's Fine Foods, LLC
- Product
- COOKED LINGUINE PASTA 6 x 5 lb Net Wt. 30lbs (13.60kg) PERIS…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
M.O.M Enterprises, LLC.
- Product
- Organic BABY bedtime drops; sleep + immunity blend; Promotes…
- Reason
- Potential yeast contamination.
- Published
- October 15, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 25, 2025Historical recordClass I
Western United Fish Company Inc
- Product
- Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193…
- Reason
- Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.
- Published
- October 15, 2025
- Distribution
- Product was sold in the following states…
View recall →
FDA Recall
OngoingHistorical recordClass II
Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 5 mL, Rx Only, Sterile, Manufactured by: Apotex Inc., Richmond Hill, Ontario, Canada, L4C 5H2, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-1003-1.
by Apotex Corp.
- Reason
- Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
- Published
- October 8, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5%, a) 5 mL and b) 10 mL, Rx Only, Sterile, Manufactured by: Apotex Inc., Richmond Hill, Ontario, Canada, L4C 5H2, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-0589-1 (5 mL), NDC 60505-0589-2 (10 mL).
by Apotex Corp.
- Reason
- Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
- Published
- October 8, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Carbamazepine Extended-Release Tablets, USP 400 mg, 30 Tablets per carton (3x10 unit dose cards), Rx Only, American Health Packaging, Columbus, OH 43217. Carton NDC 60687-594-21; (Individual Dose NDC: 60687-594-11)
by Amerisource Health Services LLC
- Reason
- Failed Dissolution Specifications.
- Published
- October 8, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Entecavir Tablets, USP, 1 mg, 30-count bottle, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-921-06.
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
- Published
- October 8, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Entecavir Tablets, USP, 0.5 mg, 30-count bottle, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-920-06.
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
- Published
- October 8, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: October 9, 2025Historical recordClass III
Stanley Pearlman Enterprises, Inc.
- Product
- NAFCO, WHITING FILLET SKIN-ON BONELESS IQF, 2 lb., Cases are…
- Reason
- Recall initiated due to the wrong best by date (1-11-2025) being printed on the retail bag which would imply that these are expired but in truth they are good until 1-11-2027.
- Published
- October 8, 2025
- Distribution
- The product was distributed to the follo…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: October 1, 2026Historical recordClass I
WFM Purchasing, LP
- Product
- Whole Foods Market Blueberry Almond Granola, PLU 86032, pack…
- Reason
- Product was incorrectly labeled, resulting in undeclared wheat, sesame, and cashew.
- Published
- October 8, 2025
- Distribution
- One retail store in Philadelphia, PA.
View recall →
FDA Recall
OngoingHistorical recordClass III
READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic, Not Sterile, 1 Gallon (3.78 L) per bottle, Manufactured in USA by Medline Industries, LP., Three Lakes Drive, Northfield, IL 60093, NDC 53329-939-25
by Medline Industries, LP
- Reason
- Subpotent drug
- Published
- October 1, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass III
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 30 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-034-01
by Granules Pharmaceuticals Inc.
- Reason
- Failed Impurities/Degradation Specifications:
- Published
- October 1, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass III
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 20 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-032-01
by Granules Pharmaceuticals Inc.
- Reason
- Failed Impurities/Degradation Specifications:
- Published
- October 1, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass III
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 15 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-031-01
by Granules Pharmaceuticals Inc.
- Reason
- Failed Impurities/Degradation Specifications:
- Published
- October 1, 2025
- 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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