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Recall totals

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

37,223

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,844

Class I recallsReasonable probability of serious health consequences

24,370

Class II recallsTemporary or medically reversible health consequences

2,896

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 6, 2026 ET

Summary (Year to date)

1,725 recalls have been announced year to date.
Sep 2026 was 7% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,370
Class I	9,844
Class III	2,896
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,370
Class I	9,844
Class III	2,896
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: Cheeseburger Sliders Product ID C47220, 470220
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product: Sam International Bulk Raw Whole Pistachio 80% VP Net Wt. 3…
Reason: Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Minnie Marie Bakers, Inc. dba Awrey's Bakery

Product: White Sponge Cake 8x12 30 lb case 20, 24oz cakes per case
Reason: Products may contain undeclared tree nuts (walnuts). People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Published: September 7, 2016
Distribution: Ohio

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FDA Recall United States Terminated Historical recordClass II

Carfagnas Inc

Product: Carfagnas Mild Chili Ready Sauce in 32 oz. glass jars.
Reason: Acidified process not on file with the FDA
Published: September 7, 2016
Distribution: Ohio only

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: Beef Sausage & Cheese Mini Bagel Sandwich Product ID C80916
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: All American Burger Product ID 470007, C47007
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product: IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. 3 lb.…
Reason: Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product: Beef Sausage Breakfast Sandwich Product ID C99018
Reason: Potential Listeria monocytogenes contamination.
Published: September 7, 2016
Distribution: U.S. distribution to the following; CA,…

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product: JUST Cinnamon Roll Coffee Cake Mix; NET WT 26.9 oz. (1 lb 1…
Reason: Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product: Valued Natural Raw Pistachio Kernels Net Wt 5 oz. (141 g) I…
Reason: Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product: JUST White Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC…
Reason: Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product: JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567…
Reason: Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published: September 7, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Minnie Marie Bakers, Inc. dba Awrey's Bakery

Product: Devils Food Sheet Cake 8x12 Mega 28.125 lb case 20, 2 2.5…
Reason: Products may contain undeclared tree nuts (walnuts). People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Published: September 7, 2016
Distribution: Ohio

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FDA Recall Terminated Historical recordClass III

Hydrocortisone and acetic acid otic solution, Rx only, 10 mL bottle, Distributed by Actavis Inc. 60 Columbia Road Bldg B. Morristown, NJ 07560 USA , NDC 45963-412-61

by Actavis Inc

Reason: Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature sample(s).
Published: August 31, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Acetasol HC (hydrocortisone and acetic acid otic solution USP) , Rx Only, 10 mL bottle, Manufactured by: Actavis Midatlantic LLC 1877 Kawai Road Lincolnton, NJ 28092 USA, NDC 0472-0882-82

by Actavis Inc

Reason: Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature sample(s).
Published: August 31, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amoxicillin for Oral Suspension USP, 400 mg/ 5 mL, 50 mL bottle, Rx only, Manufactured In Canada by: Teva Canada Limited, Toronto, Canada, NDC 0093-4161-76

by Teva North America

Reason: Superpotent drug: Out of specification test result for assay during stability testing.
Published: August 31, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only, Marketed by: VersaPharm Incorporated Marietta, GA 30062, Manufactured by: Ei LLC Kannapolis, NC 28083, NDC 61748-205-60.

by Akorn, Inc.

Reason: Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
Published: August 31, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amlodipine Besylate Tablets, USP, 10 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-452-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-452-56; and c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-452-19; Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Published: August 31, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amlodipine Besylate Tablets, USP, 5 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-451-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-451-56, c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-451-19; and d) 30-count tablets per dosage card in a carton, NDC 51079-451-69, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Published: August 31, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amlodipine Besylate Tablets, USP, 2.5 mg*, packaged in a)100-count (10 x 10) unit dose blisters per carton, NDC 51079-450-20 and b) 30-count tablets per dosage card in a carton, NDC 51079-450-63, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Published: August 31, 2016
Distribution: Nationwide

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Data last updated: October 6, 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.