FDA Recall
🇺🇸 United States
TerminatedTerminated: November 21, 2025Historical recordClass II
NuNaturals Inc
- Product
- Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Produ…
- Reason
- Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
- Published
- August 6, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 5, 2025Historical recordClass II
Moon N Sea GA LLC
- Product
- Yellow Fin Tuna, Net WT (variable weight) 50 lb brown corrug…
- Reason
- RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
- Published
- August 6, 2025
- Distribution
- Products were shipped to the following s…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 5, 2025Historical recordClass II
Moon N Sea GA LLC
- Product
- Blue Fin Tuna, Net WT (variable weight) 50 lb brown corrugat…
- Reason
- RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
- Published
- August 6, 2025
- Distribution
- Products were shipped to the following s…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 5, 2025Historical recordClass II
Moon N Sea GA LLC
- Product
- Fresh Scottish Salmon Fillet, Net WT (variable weight) 50 lb…
- Reason
- RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
- Published
- August 6, 2025
- Distribution
- Products were shipped to the following s…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 5, 2025Historical recordClass II
Moon N Sea GA LLC
- Product
- Fresh Chilean Salmon Fillet, Net WT (variable weight) 50 lb…
- Reason
- RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
- Published
- August 6, 2025
- Distribution
- Products were shipped to the following s…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: January 9, 2026Historical recordClass II
Camerican International Inc
- Product
- Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cre…
- Reason
- Undeclared Allergen (Milk). Consumer found a breaded halloumi Cheese Stick in the bag of churro bites. The Halloumi Cheese contains milk which is not an allergen in the churros.
- Published
- August 6, 2025
- Distribution
- The recalled product was distributed to…
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FDA Recall
OngoingHistorical recordClass II
Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for: Ciple USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC# 69097-319-86 (pouch), 69097-319-87 (carton)
by Cipla USA, Inc.
- Reason
- Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
- Published
- July 30, 2025
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: January 5, 2026Historical recordClass II
clomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay Boulevard, Suite 500, Naples, Florida 34108, NDC# 68180-492-01
by Lupin Pharmaceuticals Inc.
- Reason
- Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at expiry.
- Published
- July 30, 2025
- Distribution
- Nationwide
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FDA Recall
CompletedHistorical recordClass III
Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.
by Imprimis NJOF, LLC
- Reason
- Sub-Potent Drug: Subpotent assay results during stability testing.
- Published
- July 30, 2025
- Distribution
- Nationwide
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FDA Recall
CompletedHistorical recordClass II
Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01
by Imprimis NJOF, LLC
- Reason
- Sub-Potent Drug: Subpotent assay results during stability testing.
- Published
- July 30, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Mondelez Global Llc
- Product
- Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 co…
- Reason
- Undeclared allergens (Peanut) due to mispackaging
- Published
- July 30, 2025
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Mondelez Global Llc
- Product
- Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20-…
- Reason
- Undeclared allergens (Peanut) due to mispackaging
- Published
- July 30, 2025
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Mondelez Global Llc
- Product
- Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 c…
- Reason
- Undeclared allergens (Peanut) due to mispackaging
- Published
- July 30, 2025
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Mondelez Global Llc
- Product
- Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 co…
- Reason
- Undeclared allergens (Peanut) due to mispackaging
- Published
- July 30, 2025
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 18, 2025Historical recordClass II
LEWIS BAKERIES
- Product
- Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/…
- Reason
- Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts.
- Published
- July 30, 2025
- Distribution
- Product was distributed to: TN, KS, AR,…
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FDA Recall
OngoingHistorical recordClass II
Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant, 1.8 oz./ 53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-040-00 UPC Code 815195018224
by A.P. Deauville, LLC
- Reason
- CGMP Deviations
- Published
- July 23, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Beauty & Skincare Power Stick original nourishing invisible protection roll-on Antiperspirant/Deodorant Spring Fresh, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-039-00, UPC Code 815195018194
by A.P. Deauville, LLC
- Reason
- CGMP Deviations
- Published
- July 23, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313
by A.P. Deauville, LLC
- Reason
- CGMP Deviations
- Published
- July 23, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Rizatriptan Benzoate Tablets, USP, 10 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ 07054, NDC 67877-262-18
by Ascend Laboratories, LLC
- Reason
- CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
- Published
- July 23, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Rizatriptan Benzoate Tablets, USP, 5 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ 07054, NDC 67877-261-18
by Ascend Laboratories, LLC
- Reason
- CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
- Published
- July 23, 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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