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Recall totals

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

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 11, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules, CII 20 mg, 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-832-25; Blister NDC 68084-832-95

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 15 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-898-32; Blister NDC 68084-898-33

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 10 mg 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-815-25; Blister NDC 68084-815-95

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 30 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 60687-154-25; Blister NDC 60687-154-95

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 20 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-943-25; Blister NDC 68084-943-95

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 15 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 60687-133-25; Blister NDC 60687-133-95

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 10 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-936-25; Blister NDC 68084-936-95

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 18, 2017Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 5 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-874-25; Blister NDC 68084-874-95

by Amerisource Health Services

Reason: Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 20, 2016Historical recordClass II

Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection, 10 mL multidose vial, sterile. Rx only. Compounded by Isomeric Pharmacy Solutions, Salt Lake City, UT 84109,

by Isomeric Pharmacy Solution, LLC

Reason: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a voluntary field action for the Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection because the sterile injectable products were sterilized too long leading to potential difficulty resuspending particles.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 30, 2016Historical recordClass II

Superior Foods

Product: Archer Farms Quinoa 10 oz packaged in flexible plastic bag
Reason: Product contains undeclared wheat
Published: September 14, 2016
Distribution: Multiple states

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FDA Recall United States OngoingHistorical recordClass II

Inland Seafood, Inc.

Product: Inland Market, Premium, Maine Lobster Spread, Net Wt. 7 oz.…
Reason: Possible contamination with foreign matter; wood pieces.
Published: September 14, 2016
Distribution: CT, FL, GA, MA, MD, NC, NJ, NY, PA, SC,…

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FDA Recall United States TerminatedTerminated: April 10, 2017Historical recordClass II

Pharmavite

Product: Nature Made(R) adult gummies Multi for Her plus Omega-3, 150…
Reason: Specific lots of Nature Made(R) product may have possible Salmonella contamination.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 22, 2019Historical recordClass II

McCain Foods USA

Product: Fire roasted Poblano & Jalapeno popper bites packaged in a w…
Reason: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 10, 2017Historical recordClass II

Pharmavite

Product: Nature Made(R) D3 1000IU, 350 count, UPC 0-31604-04070-3
Reason: Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States CompletedHistorical recordClass II

Geneva Foods, LLC

Product: Lysander's All Natural Bourbon Flavor Rub; for beef, chicken…
Reason: Product contains undeclared allergens soy and wheat. Also does not declare sulfites.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Inland Seafood, Inc.

Product: Inland Market, Traditional Crab Cake, Net Wt. 5 lbs, Inland…
Reason: Possible contamination with foreign matter; wood pieces.
Published: September 14, 2016
Distribution: CT, FL, GA, MA, MD, NC, NJ, NY, PA, SC,…

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FDA Recall United States TerminatedTerminated: April 10, 2017Historical recordClass II

Pharmavite

Product: Nature Made(R) Multi + Omega-3, 150 count, UPC 0-31604-04173…
Reason: Specific lots of Nature Made(R) product may have possible Salmonella contamination.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 10, 2017Historical recordClass II

Pharmavite

Product: Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC…
Reason: Specific lots of Nature Made(R) adult gummies Hair.Skin.Nails may exceed specifications total viable plate count.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 10, 2017Historical recordClass II

Pharmavite

Product: Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2
Reason: Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Published: September 14, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 22, 2019Historical recordClass II

McCain Foods USA

Product: Breaded stuffed Jalapenos poppers labeled in part: Anchor br…
Reason: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Published: September 14, 2016
Distribution: Nationwide

View recall →

Data last updated: November 11, 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.