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Recall totals

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

37,139

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 25, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass I

LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.

by EZWeightLossTX LLC

Reason: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these unapproved drugs.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Lorazepam Oral Concentrate, USP, 2 mg/mL, 30 mL bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Branchburg, NJ 08876. Distributed by: Amneal Pharmaceuticals, Glasgow, KY 42141. NDC 65162-687-84

by Amneal Pharmaceuticals of New York, LLC

Reason: Defective Delivery System: the dropper measurement markings may be reversed, shifted or missing.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (200 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-61.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj, USP QS 5 mL (200 mcg per mL), 5 mL Sterile single dose syringe, packaged in 8 x 5 (FORTY) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-67.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin 100 mcg/mL QS 5% Dextrose Inj, USP (2 mg per 20 mL) 20 mL Sterile single dose syringe, packaged in 10 x 5 (FIFTY) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-818-62.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (100 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-818-61.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (200 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-61.

by Advanced Pharma Inc.

Reason: Subpotent Drug: found to be below the specification for labeled assay.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj, USP QS 5 mL (200 mcg per mL), 5 mL Sterile single dose syringe, packaged in 8 x 5 (FORTY) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-67.

by Advanced Pharma Inc.

Reason: Subpotent Drug: found to be below the specification for labeled assay.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (100 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-818-61.

by Advanced Pharma Inc.

Reason: Subpotent Drug: found to be below the specification for labeled assay.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.25% Acetic Acid Irrigation USP, 500 mL Plastic Irrigation Container (PIC), B. Braun Medical Inc. Irvine CA 92614-5895 USA, NDC 0264-2304-10

by B. Braun Medical Inc

Reason: Presence of Particulate Matter: identified as polyethylene, which is consistent with the material used to manufacture the contain cap
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Extended-release Tablets, USP 54 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC 13811-709-10

by Osmotica Pharmaceutical Corp

Reason: Subpotent Drug
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC 13811-707-10

by Osmotica Pharmaceutical Corp

Reason: Subpotent Drug
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Creative Contract Packaging Corporation, LLC

Product: HERB-OX Beef Flavor Granulated Bouillon, 4 ounce jars
Reason: Creative Contract Packaging LLC is voluntarily recalling two code dates of HERB-OX Beef Flavor Granulated Bouillon, due to the potential presence of an undeclared milk allergen.
Published: December 27, 2017
Distribution: Domestic: AZ, CA, CO, CT, DE, IA,ID, IN,…

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FDA Recall United States Terminated Historical recordClass III

The Hain Celestial Group, Inc. - Worldwide HQ

Product: BluePrint ORGANIC Beet Blast Vegetable & Fruit Drink 16 fl.o…
Reason: The label on the back of the bottle may be for the incorrect product.
Published: December 27, 2017
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass II

Riomet (metformin hydrochloride) Oral Solution Cherry Flavored 500 mg /5 mL, 4 fl. oz. (NDC 10631-206-01) and 16 fl. oz. (NDC 10631-206-02) HDPE bottles, Rx only, Manufactured for: Ranbaxy Laboratories Inc. Jacksonville, FL 32257 USA, Distributed by: Sun Pharmaceutical Industries, Cranbury, NJ 08512

by Sun Pharmaceutical Industries, Inc.

Reason: Microbial Contamination of Non-Sterile Products
Published: December 20, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Penicillin V Potassium for Oral Solution, USP, 125 mg (200,000 U) per 5 mL, 100 mL (when mixed) bottle, Rx only, Manufactured In Canada By: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454; NDC 0093-4125-73.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: high out of specification test results obtained for individual and total impurities.
Published: December 20, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wang Globalnet

Product: Fish Cake in Polybag 10/930g, Item no. 15731 UPC Code 08770…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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FDA Recall United States Terminated Historical recordClass I

Wang Globalnet

Product: Fish Cake in Polybag 10/2.2lbs, Item no. 12842 UPC Code 087…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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FDA Recall United States Terminated Historical recordClass I

Wang Globalnet

Product: Fish Tofu in Polybag 40/240g, Item no. 17185, UPC Code 08770…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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FDA Recall United States Terminated Historical recordClass I

Wang Globalnet

Product: Fish Ball in Polybag 24/12oz., Item no. 20072, UPC Code 0877…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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Data last updated: September 25, 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.