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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: CO ×
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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 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 I

Aquamar Inc

Product: Kanimi Crab Flavored Seafood Fancy Shred Style 92410 Ingredi…
Reason: Product found to contain undeclared wheat and eggs
Published: June 28, 2023
Distribution: U.S. distribution to the following: AZ,…

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FDA Recall United States Terminated Historical recordClass I

Aquamar Inc

Product: Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM…
Reason: Product found to contain undeclared wheat and eggs
Published: June 28, 2023
Distribution: U.S. distribution to the following: AZ,…

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FDA Recall United States Terminated Historical recordClass I

Aquamar Inc

Product: Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ing…
Reason: Product found to contain undeclared wheat and eggs
Published: June 28, 2023
Distribution: U.S. distribution to the following: AZ,…

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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 United States Terminated Historical recordClass II

T.W. GARNER FOOD CO

Product: Texas Pete BUFFALO Wing Sauce 12 FL OZ - 355 mL TW GARNER FO…
Reason: The product contains undeclared soybean oil and soy lecithin.
Published: June 21, 2023
Distribution: Product was shipped to the following sta…

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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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FDA Recall Terminated Historical recordClass II

Travoprost Ophthalmic Solution, USP (Ionic Buffered Solution), 0.004%, Rx only, Manufactured by Apotex Inc., Manufactured by: GSMS Incorporated, Camarillo, CA 93012, a) NDC 51407-731-25 (2.5 mL bottle), b) NDC 51407-731-05 (5 mL bottle).

by Golden State Medical Supply Inc.

Reason: Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary container.
Published: June 14, 2023
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

ASCORBIC ACID PRESERVED INJECTION SOLUTION, 500 mg/mL, 30 mL Sterile Multiple-Dose Vial, RX ONLY, Compounded by: Empower Pharmacy, 5980 W Sam Houston Pkwy N Ste 300 Houston, TX 77041, NDC 72627-2405-1

by Empower Clinic Services LLC dba Empower Pharmacy

Reason: Mislabeling: preservative free product labeled as preserved.
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.