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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

36,950

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,732

Class I recallsReasonable probability of serious health consequences

24,263

Class II recallsTemporary or medically reversible health consequences

2,873

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,071 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 2026

Most affected stateHawaii 200 recalls mention this state

State: RI ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 7, 2026 ET

Summary (Year to date)

1,458 recalls have been announced year to date.
Aug 2026 was 53% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

FDA Recall United States Terminated Historical 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 Ongoing Historical 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 Terminated Historical 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 Completed Historical 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 Completed Historical 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

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FDA Recall United States Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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

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FDA Recall Ongoing Historical 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

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FDA Recall Ongoing Historical 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

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FDA Recall Ongoing Historical 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 Ongoing Historical 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

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FDA Recall Ongoing Historical recordClass II

Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 100-count bottles, Rx only, Mfg for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202, Manufactured by: Lupin Limited Nagpur-441 108, INDIA, NDC 68180-519-01

by Lupin Pharmaceuticals Inc.

Reason: Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.
Published: July 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Omeprazole Delayed-release Capsules, USP, 20mg, 1000-count bottle, Rx Only, Manufactured by: Dr. Reddy's Laboratories Limited, Bachupally - 500 090 INDIA, Manufactured for: Qualient Pharmaceuticals Health LLC, Grand Cayman, Cayman Islands, NDC 82009-022-10. NDC 82009-022-10

by Dr. Reddy's Laboratories, Inc.

Reason: Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
Published: July 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-456-17

by ACCORD HEALTHCARE, INC.

Reason: Subpotent Drug: Assay below the approved specification
Published: July 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-455-17

by ACCORD HEALTHCARE, INC.

Reason: Subpotent Drug: Assay below the approved specification
Published: July 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-452-17

by ACCORD HEALTHCARE, INC.

Reason: Subpotent Drug: Assay below the approved specification
Published: July 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-451-17

by ACCORD HEALTHCARE, INC.

Reason: Subpotent Drug: Assay below the approved specification
Published: July 23, 2025
Distribution: Nationwide

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Data last updated: September 7, 2026 ET

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. Read the full medical disclaimer.