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Recall totals

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

37,136

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/berlin-seeds-recalls-alfalfa-sprouting-seed-because-possible-health-riskPublished September 23, 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 23, 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

Paliperidone Extended-Release Tablets, 3 mg, 90 count bottles, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA, NDC: 0591-3693-19

by Teva Pharmaceuticals

Reason: Failed Dissolution Specifications: Drug release test result, obtained during routine 9-month stability testing, which was below specification for one tablet. Teva cannot at this time exclude the potential for additional tablets to be below specification.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and Pfizer Inc. New York, NY 10017 USA, NDC 0003-0894-21

by Bristol-Myers Squibb Company

Reason: Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

BRILINTA (ticagrelor) tablets, 90 mg, 8-count Professional Sample bottles, Rx only, Mfd. for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850; By: AstraZeneca AB, SE-151 85 Sodertalje, Sweden, NDC 0186-0777-08.

by AstraZeneca Pharmaceuticals, LP

Reason: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count professional sample bottle labeled as BRILINTA 90 mg tablets contained 5 ZURAMPIC 200 mg tablets, in addition to the expected 8 BRILINTA tablets.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015; Distributed in Canada by Baxter Corporation, Toronto, Ontario, Canada, Product Code: 2B1322, NDC 0338-0049-02.

by Baxter Healthcare Corporation

Reason: Lack of Assurance of Sterility: Customer complaints for leaking bags.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 15 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-922-25

by Advanced Pharma Inc.

Reason: Lack of Assurance of Sterility
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 30 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-924-25

by Advanced Pharma Inc.

Reason: Lack of Assurance of Sterility
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 20 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-926-25

by Advanced Pharma Inc.

Reason: Lack of Assurance of Sterility
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

QUELICIN (Succinylcholine Chloride) Injection, USP 20 mg/mL in a) 5 mL vial (NDC 15082-814-67), b) 7mL vial (NDC 15082-814-79), c) 10mL vial (NDC 15082-814-61), Repackaged by Advanced Pharm, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404.

by Advanced Pharma Inc.

Reason: Lack of Assurance of Sterility
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

NatureBox, Inc.

Product: NatureBox Mini Crispy Snickerdoodles: Cinnamon-sugar cookie…
Reason: One piece of a cashew was found during packing of Mini Crispy Snickerdoodle snack product.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wildway LLC

Product: Trader Joe's Grainless Granola 8 oz. (SKU 56307) packaged i…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

3CS ORGANICS LLC

Product: Lebenswert Bioland Anfangsmilch1, 500g (4/case), Lebenswert…
Reason: The product is not FDA approved and not all products are labeled in English.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

3CS ORGANICS LLC

Product: HOLLE Bio Lait Pour Nourrissons Au Lait De Chevre, Zuigeling…
Reason: The product is not FDA approved and not all products are labeled in English.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

3CS ORGANICS LLC

Product: HIPP Tetrapack-Liquid , Single Serve Combiotik Hungry Infant…
Reason: The product is not FDA approved and not all products are labeled in English.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

3CS ORGANICS LLC

Product: HIPP Organic Comb Hungry Infant Milk, 800g (4bx/case), HIPP…
Reason: The product is not FDA approved and not all products are labeled in English.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

3CS ORGANICS LLC

Product: HIPP Anti-Reflux AR Bio-Spezialnahrung, 500g (4/case)
Reason: The product is not FDA approved and not all products are labeled in English.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Threshold Enterprises Ltd

Product: Source Naturals Renewal Antioxidant Tablet: 10 Count Sample…
Reason: Dietary supplements contain low levels of undeclared boron
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Threshold Enterprises Ltd

Product: Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30…
Reason: Dietary supplements contain low levels of undeclared boron
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wildway LLC

Product: Wildway Vanilla Bean Espresso Grain-free Granola 8 oz. UPC…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wildway LLC

Product: Wildway Coconut Cashew Grain-free Granola 8 oz. and 10 oz. U…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: July 19, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wildway LLC

Product: Wildway Banana Nut Grain-free Granola 8 oz. UPC: 85866000517…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: July 19, 2017
Distribution: Nationwide

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Data last updated: September 23, 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.