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Recall totals

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

37,113

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 15, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass II

Riverside Natural Foods, Ltd.

Product: Good & Gather Banana Chocolate Chip Date & Nut Bars, UPC 0 8…
Reason: The product contains an undeclared almonds.
Published: December 16, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Anagrelide Capsules, USP 1 mg, 100 capsules, Rx only, Manufactured in India for: Torrent Pharma Inc., Basking Ridge, NJ 07920 NDC 13668-462-01

by Torrent Pharma Inc

Reason: Failed Dissolution Specifications
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clobetasol Propionate Ointment USP 0.05%, Net Wt. 50 grams, Rx Only, Teligent Pharma. Inc. Buena, NJ 08310 NDC 52565-039-60

by Teligent Pharma, Inc.

Reason: Superpotent and Subpotent; low and high assay results
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

REGENECARE HA (Lidocaine HCL 2%) Topical Anesthetic Hydrogel, Net Wt. 3 oz. (85 g), Manufactured For: MPM Medical Mesquite, TX 75149. NDC 66977-107-03

by MPM Medical LLC

Reason: Microbial Contamination of Non-Sterile Drug Product. The product was found to be contaminated with the bacteria Burkholderia cepecia.
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Levocetirizine Dihydrochloride Tablets, USP, 5 mg 30-count bottle, Rx Only, Distributed by: Marlex Pharmceuticals, Inc. New Castle, DE 19720. NDC 10135-0639-30

by InvaTech Pharma Solutions, LLC

Reason: Failed Impurities/Degradation Specifications: One lot of Levocetirizine dihydrochloride tablets 5 mg 30 count failed stability testing.
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Aripiprazole Tablets, USP, 15 mg, 30 tablets per unit dose carton, Rx Only, Manufactured by: Apotex, Inc, Toronto, Ontario Canada M9L 1T9, Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA, NDC 0904-6512-04

by The Harvard Drug Group

Reason: Failed Dissolution Specifications: Out of specification for dissolution.
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ARIPIPRAZOLE TABLETS, 15 mg, 30-count. bottles, Rx Only, GSMS Incorporated, Manufactured by: Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS, Incorporated, Camarillo, CA 93012 USA, NDC #60429-449-30

by Golden State Medical Supply Inc.

Reason: FAILED DISSOLUTION SPECIFICATIONS: Possibility of out-of-specification (OOS) dissolution limits for the remaining shelf life of the Aripiprazole Tablets
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Tucson Tamale Wholesale Company, LLC

Product: Tucson Tamale Blue Corn, Veggie & Cheese Tamales (2 Pack), 1…
Reason: Plastic pieces (1-2 cm) were discovered inside cans of tomatoes which were used to make two types of tamales.
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Tucson Tamale Wholesale Company, LLC

Product: Tucson Tamale Blue Corn & Veggie Tamales (2 Pack), 11 OZ (31…
Reason: Plastic pieces (1-2 cm) were discovered inside cans of tomatoes which were used to make two types of tamales.
Published: December 9, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Triamcinolone Acetonide Lotion USP, 0.025%, 60 mL (60 grams) bottle, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-010-59

by Teligent Pharma, Inc.

Reason: Subpotent Drug: One lot of Triamcinolone Acetonide Lotion, 0.025% 60 mL.does not meet assay results.
Published: December 2, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levetiracetam Tablets, USP 500 mg, packaged in 120-count bottle, Rx only, Manufactured by: VKT Pharma Private Limited Srikakulam, India - 532 409, Manufactured for: Eywa Pharma Inc. 2 Research Way, Floor 3 Princeton, NJ 08540, NDC 71930-063-52

by EYWA PHARMA INC

Reason: Presence of foreign tablet/capsule: A 1000 mg Levetiracetam Tablet was found in 500 gram bottle of Levetiracetam Tablets.
Published: December 2, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Felodipine Extended Release Tablets, USP 10 mg,100-count bottle, Rx only, Distributed by: Heritage Pharmaceuticals Inc. East Brunswick, NJ 08816 Made in India, NDC 23155-050-01

by Heritage Pharmaceuticals Inc

Reason: Failed impurities/ degradation specifications: Out of specification impurity results were observed during routine testing of stability samples for the impurity Felodipine Related compound A
Published: December 2, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Immune Boost with natural strawberry flavor, 8,000 IU, Supports a Healthy and Balanced Immune System, 60 mL bottle, Manufactured by: Fusion Health and Vitality, LLC. 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004.

by Fusion Health and Vitality LLC

Reason: Marketed without an Approved NDA/ANDA: Product marketed with drug claims.
Published: December 2, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

DOXOrubicin Hydrochloride Injection, USP, 10 mg / 5 mL (2 mg / mL), 5 mL fill in a 6 mL vial, Single Dose Vial, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047. NDC: 63323-883-05

by Fresenius Kabi USA, LLC

Reason: Cross Contamination with Other Products: trace amounts of octreotide found during testing
Published: December 2, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

clomiPRAMINE Hydrochloride Capsules USP, 50 mg, 30-count bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD NDC 59746-711-30

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Failed Tablet/Capsule Specification
Published: December 2, 2020
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473 mL) NDC 52376-021-02; b) 4 fl oz (118 mL) NDC 52376-021-04, Sunstar Americas, Inc.

by Sunstar Americas, Inc.

Reason: Microbial Contamination of Non-sterile Products: contamination with Burkholderia lata.
Published: December 2, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Aripiprazole Tablets, USP 15 mg tablets, packaged in a) 1000 count bottle, NDC 60505-2675-8; b) 30 count bottle, NDC 60505-2675-3; Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326

by Apotex Corp.

Reason: Failed Dissolution Specifications: Out of specification for dissolution.
Published: November 25, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sodium Chloride Injection, USP, 0.9%, 0.308 mOsmol/mL, 2mL Single Dose Vial, Preservative Free, For use as a sterile diluent, Rx Only, Mfd. by. West-ward Eatontown, NJ 07724 USA, a) Vial NDC 0641-0497-17, b) Carton of 25 vials NDC 0641-0497-25.

by Hikma Pharmaceuticals USA Inc.

Reason: Failed pH Specifications: Out of Specification pH Test Results were found in Sodium Chloride Injection USP 0.9% 2 mL vial.
Published: November 25, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Testosterone Gel 1%, 2.5 grams per unit dose, packaged in 2.5 gram Unit-Dose Packets (NDC 0591-3216-17); 30 Unit-Dose Packets per carton (NDC 0591-3216-30), Rx only, Manufactured by: Actavis Laboratories UT, Inc., Salt Lake City, UT 84108; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054.

by Teva Pharmaceuticals USA

Reason: Superpotent Drug: High out-of-specification assay results were obtained during stability testing.
Published: November 25, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01

by Ascent Pharmaceuticals, Inc.

Reason: Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and Acetaminophen Tablets USP 10mg/325 mg contains one Losartan Potassium Tablets, USP 100 mg.
Published: November 25, 2020
Distribution: Nationwide

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Data last updated: September 15, 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.