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Recall totals

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

37,142

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 26, 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.

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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 United States Terminated Historical recordClass II

Simply Delicious, Inc. dba Bobo's Oat Bars

Product: Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per…
Reason: Bobo's recalled Coconut 3oz Bar due to mold.
Published: February 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product: Panera Reduced-Fat Plain Cream Cheese, 2 oz. and 8 oz.
Reason: Product may be contaminated with Listeria monocytogenes.
Published: February 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product: Panera Plain Cream Cheese, 2 oz. and 8 oz.
Reason: Product may be contaminated with Listeria monocytogenes.
Published: February 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

CHOBANI

Product: Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogur…
Reason: Product is recalled because a statement on the overwrap label erroneously states "No Gluten" while the ingredients statement and the Contains statements on both the overwrap label and the flip label on each individual cup declare wheat.
Published: February 14, 2018
Distribution: distributed in AL, AR, AZ, CA, CO, CT,…

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FDA Recall United States Terminated Historical recordClass II

Palmer and Company

Product: Sea Salt Caramel Hearts, Net Wt 12 OZ (340 g), Made by Palme…
Reason: During packaging, the firm observed a peanut stuck to the outside of caramel heart. Peanuts are not declared on the label.
Published: February 14, 2018
Distribution: Product distributed to one distribution…

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FDA Recall Terminated Historical recordClass I

Nexterone (amiodarone HCl) Premixed Injection, 150mg/100mL, 100-mL bag, Rx Only, Sterile, Baxter Healthcare Corporation, Deerfield, IL. NDC 43066-150-10

by Baxter Healthcare Corporation

Reason: Presence of Particulate Matter:Particulate identified as polyethylene, the primary constituent of the film and ports used to manufacture the bag in which product is packaged
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Clopidogrel Tablets, USP 75 mg, 30-count bottles, Rx only, Packaged for: International Laboratories, LLC St. Petersburg, FL 33710, NDC 54458-888-16

by International Laboratories, LLC

Reason: LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles labeled as Clopidogrel tablets, USP 75 mg.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Vecuronium bromide for Injection, 10 mg vials, Rx only, Mfd. for: Fresenius Kabi, Lake Zurich, IL 60047, Made in India, NDC 63323-781-10

by Fresenius Kabi USA, LLC

Reason: Failed impurities/ degradation specifications: Out-of-specification (OOS) result for USP related compound F at the 12 month stability test station.
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium Tablets 40 mg, 90 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories, Ltd., Srikakulam, INDIA --- NDC 55111-123-05

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium Tablets 20 mg, a) 90 count and b) 500 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories, Ltd., Srikakulam, INDIA --- NDC 55111-122-05

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability
Published: February 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III