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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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: KS ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 13, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

Kanjo Homeopathic Pain Relief Cream With Arnica, NET WT 2 oz (56.70G), Manufactured For: Acutens, Inc., Sheridan, WY NDC 80551-201-02

by Homeocare Laboratories, Inc.

Reason: cGMP deviations
Published: July 5, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Endometrin (progesterone) Vaginal Insert 100mg, packaged in a carton of 21 vaginal inserts with 21 disposable vaginal applicators, Manufactured for: Ferring Pharmaceuticals Inc., Parsippany, NJ NDC# 55566-6500-03

by Ferring Pharmaceuticals Inc

Reason: cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
Published: July 5, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count Tablets Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Distributed by: Major Pharmaceuticals Livonia, MI 48152 USA, NDC 0904-7179-61

by The Harvard Drug Group

Reason: Packaging defect: blister packaging inadequately sealed.
Published: July 5, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Richin Trading Inc

Product: Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; It…
Reason: Potential choking hazard
Published: July 5, 2023
Distribution: Distributed to locations in AZ, CA, CO,…

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FDA Recall United States Terminated Historical recordClass I

Richin Trading Inc

Product: Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Ite…
Reason: Potential choking hazard
Published: July 5, 2023
Distribution: Distributed to locations in AZ, CA, CO,…

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FDA Recall United States Terminated Historical recordClass I

Richin Trading Inc

Product: Sun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan;…
Reason: Potential choking hazard
Published: July 5, 2023
Distribution: Distributed to locations in AZ, CA, CO,…

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FDA Recall United States Terminated Historical recordClass II

Rudolph Foods Company

Product: Rudolphs OnYums Onion Flavored Snack Rings 3 oz. UPC 0-24…
Reason: Undeclared wheat and artificial colors (Yellow 6, Yellow Lake 6, Blue 2 Lake, Blue 1 Lake, Red 40 Lake)
Published: July 5, 2023
Distribution: Arkansas, Colorado, Illinois, Indiana, I…

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FDA Recall United States Terminated Historical recordClass III

Anatox Inc

Product: Sonne's Detoxificant #7, 1 quart (946 mL) packaged in amber…
Reason: Elevated lead levels
Published: July 5, 2023
Distribution: Distributors, retailers, and consumers i…

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FDA Recall United States Terminated Historical recordClass III

Anatox Inc

Product: 1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an ambe…
Reason: Elevated lead levels
Published: July 5, 2023
Distribution: Distributors, retailers, and consumers i…

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FDA Recall Terminated Historical recordClass I

ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg, Unit Dose Carton 40 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited Bachupally-500 090 India, Distributed by: Major Pharmaceuticals Livonia, MI 48152 USA, NDC 0904-6269-08

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

Reason: Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.
Published: June 28, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Glycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01

by Aurolife Pharma, LLC

Reason: Failed Impurities/Degradation Specifications
Published: June 28, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

ENTRINSIC HEALTH SOLUTION INC

Product: enterade Advanced Oncology Formula; Original Vanilla Flavor;…
Reason: Potential for the product to develop mold and spoil.
Published: June 28, 2023
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Nutricia North America

Product: TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g)…
Reason: Infant formula contains undeclared tyrosine
Published: June 28, 2023
Distribution: Alaska, California, Connecticut, Florida…

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FDA Recall Ongoing Historical recordClass III

Tranexamic Acid USP Tablets, 650 mg, 30 tablets (3X10) Unit Dose, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-772-13

by AVKARE LLC

Reason: Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Published: June 21, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

SOFT HANDS Alcohol Antiseptic 80%, Topical Solution, HAND SANITIZER, NON-STERILE SOLUTION, cleanpro SUPPLY, 1 US gallon / 3785.41ml, plastic gallon bottle, MCS Midwest Cleaning Solutions, 404 Noid Rd., Canton, SD 57013.

by Jarman's Midwest Cleaning Systems, Inc.

Reason: Chemical Contamination: FDA testing found Presence of methanol
Published: June 21, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Alcohol Antiseptic 80%, Topical Solution, Hand Sanitizer, Non-sterile Solution, Volume: 3.785 L, plastic gallon bottle, MCS Midwest Cleaning Solutions, 404 Noid Rd., Canton, SD 57013.

by Jarman's Midwest Cleaning Systems, Inc.

Reason: Chemical Contamination: FDA testing found Presence of methanol
Published: June 21, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Isopropyl Alcohol Antiseptic 75%, Topical Solution, Hand Sanitizer Non-sterile Solution, Volume: 3.785 L, plastic gallon bottle, MCS Midwest Cleaning Solutions, 404 Noid Rd., Canton, SD 57013. NDC: 74663-002-01

by Jarman's Midwest Cleaning Systems, Inc.

Reason: CGMP deficiencies: Product manufactured at the same site where FDA testing found Presence of methanol in other products.
Published: June 21, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lysteda (tranexamic acid) USP Tablets, 650 mg, 30 tablets per bottle, Rx Only, Manufactured for: Amring Pharmaceuticals Inc. Berwyn, PA 19312, NDC 69918-301-30

by Amring Pharmaceuticals Inc

Reason: Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Published: June 21, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

HU PRODUCTS

Product: Hu Vanilla Crunch Dark Chocolate bar
Reason: may contain undeclared tree-nuts
Published: June 21, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Buprenorphine Sublingual Tablets, 8 mg, 30 count-bottles, Rx only, Manufactured by: Sun Pharma, NDC 62756-460-83.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: CGMP Deviations
Published: June 14, 2023
Distribution: Nationwide

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Data last updated: September 13, 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.