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Recall totals

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

37,339

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,860

Class I recallsReasonable probability of serious health consequences

24,450

Class II recallsTemporary or medically reversible health consequences

2,901

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 2,095 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/imperio-distribution-llc-recalls-beef-jerky-products-produced-without-benefitPublished October 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 27, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product: FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADR…
Reason: Unapproved Drug Claims.
Published: September 24, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: January 16, 2026Historical recordClass I

Neuhaus nv

Product: NEUHAUS brand ORIGINAL BELGIAN CHOCOLATE; POPPING MILK CHOCO…
Reason: Product contains undeclared wheat.
Published: September 24, 2025
Distribution: VA, MD, PA, NY, and Washington DC

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FDA Recall United States TerminatedTerminated: December 18, 2025Historical recordClass II

Abdallah Incorporated

Product: Cream Caramels, Milk, Item ID: 2210L. Packed On (YYMMDD):…
Reason: Undeclared allergen (peanut, pecan).
Published: September 24, 2025
Distribution: PA

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FDA Recall United States TerminatedTerminated: December 18, 2025Historical recordClass II

Abdallah Incorporated

Product: Sea Salt Caramel Dark Miniature, Item ID: 2237 ML. Packed…
Reason: Undeclared allergen (peanut, pecan).
Published: September 24, 2025
Distribution: PA

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FDA Recall OngoingHistorical recordClass II

chloroproMAZINE Hydrochloride Tablets, USP, 100 mg, 50 Tablets (5x10) unit dose carton, Rx only, Manufactured for: AvKare, Pulaski, TN, 38478, NDC 50268-165-15

by AvKARE

Reason: Presence of a foreign substance.
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

chloroproMAZINE Hydrochloride Tablets, USP, 50 mg, 50 Tablets (5x10) unit dose carton, Rx only, Manufactured for: AvKare, Pulaski, TN, 38478, NDC 50268-164-15

by AvKARE

Reason: Presence of a foreign substance.
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Mineral SkinScreen, Zinc Oxide 22.75%, 15 mL, 0.5 fl. oz. per tube, Supreme Sunscreen SPF 50, 15 mL 0.5 fl. oz. per tube, Distributed by: Grace & Fire USA Inc., 251 Little Falls Drive, New Castle Wilmington, Delaware 19808, NDC 84803-110-01 (15 mL Velvet Screen), UPC 9355909005757.

by GRACE & FIRE PTY LTD

Reason: Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, Zinc Oxide 22.75%, a) 15 mL, 0.5 fl. oz. per tube, NDC 84803-106-01, UPC 9355909006068, b) 50 mL, 1.7 fl. oz. per tube, NDC 84803-106-02, UPC 9355909005924, Distributed by: Grace & Fire USA Inc., 251 Little Falls Drive, New Castle Wilmington, Delaware 19808.

by GRACE & FIRE PTY LTD

Reason: Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 200 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141. NDC: 16714-051-01

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 200 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1133-1

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 100 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141. NDC: 16714-050-01

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 100 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1132-1

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 50 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141. NDC: 16714-049-01

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 50 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1131-1

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 25 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141. NDC: 16714-048-01

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 25 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1130-1

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 10 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141. NDC: 16714-047-01

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Chlorpromazine Hydrochloride Tablets, USP, 10 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1129-1

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Sulfamethoxazole and Trimethoprim, USP, 800 mg/160 mg, Double Strength, 10 Tablets unit dose blister pack (10x1) per bag, Rx only, Distributed by Cardinal Health, Dublin, OH 43017, NDC 55154-7895-0 (Outer Bag) containing NDC 0904-2725-61 (Inner blisters).

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Sulfamethoxazole and Trimethoprim, USP, 800 mg/160 mg, Double Strength, 100 Tablets unit dose blister packs (10x10) per carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-2725-61

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Published: September 17, 2025
Distribution: Nationwide

View recall →

Data last updated: October 27, 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.