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Recall totals

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

37,211

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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: NY ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 4, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product: Kemps YO2 Frozen Yogurt Mudslide, One Pint, UPC 41483-04121
Reason: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published: May 24, 2017
Distribution: AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Oberlander Baking Co

Product: Oberlander Bakery Gluten Free Brand Chocolate Kokosh Cake N…
Reason: Oberlander Gluten Free Brand Chocolate Kokosh Cake chocolate filled cake may contain undeclared almond.
Published: May 24, 2017
Distribution: CA, FL , MD, IL, NJ and NY

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FDA Recall United States Terminated Historical recordClass II

McCain Foods USA

Product: Wegman's O'Brien Hash Browns, frozen packages, net wt. 28 o…
Reason: Wegman's O'Brien Hash Browns product, lot B161021, is recalled because it may contain golf ball materials, specifically hard plastic or rubber pieces.
Published: May 24, 2017
Distribution: Distributed in Maryland, Massachusetts,…

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FDA Recall Terminated Historical recordClass II

Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose Blisters per carton (NDC 0093-4359-93), Individual Blister Pack (NDC 0093-4359-19), Rx Only, Manufactured By: Teva Pharmaceutical Industries Ltd., Jerusalem, 9777600, Israel

by Teva Pharmaceuticals USA

Reason: Microbial Contamination of Non-Sterile Products
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PrednisoLONE Oral Solution USP, 15 mg/5mL, alcohol content: 5%(v/v) 240 mL bottle, Rx Only, Manufactured in Canada By: CONTRACT PHARMACEUTICALS LIMITED CANADA, Ontario, Canada, L5N 6L6, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-6118-87

by Teva Pharmaceuticals USA

Reason: Failed Stability Specifications
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 20 mg, packaged in a) 30-count bottles (NDC 62756-556-83), b) 100-count bottles (NDC 62756-556-88), and c) 1000-count bottles (NDC 62756-556-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, 350 Gujarat, India.

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 10 mg, packaged in a) 30-count bottles (NDC 62756-554-83), b) 100-count bottles (NDC 62756-554-88), and c) 1000-count bottles (NDC 62756-554-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, 350 Gujarat, India, NDC 62756-551-18.

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 7.5 mg, packaged in a) 30-count bottles (NDC 62756-553-83), b) 100-count bottles (NDC 62756-553-88), and c) 1000-count bottles (NDC 62756-553-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, 350 Gujarat, India.

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 2.5 mg, 1000-count bottles, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-551-18.

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Buprenorphine HCI Injection, 0.3 mg/mL, 1 mL Single Dose Vial (NDC 42023-179-01), packaged in 1 mL x 5 Single Dose Vials per carton (NDC 42023-179-05), Rx Only, Distributed by: Par Pharmaceuticals Companies, Inc., Spring Valley, NY 10977.

by Par Sterile Products LLC

Reason: Crystallization: due to the presence of white, crystalline particulates, adhered to the side and bottom of the glass vials, which are comprised of principally dextrose and the buprenorphine active component.
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

IC-Green (indocyanine green for injection, USP), 25 mg, packaged in a kit containing six vials of 25 mg lyophilized powder, Rx only, Manufactured by: Akorn, Inc., NDC 17478-701-02

by Akorn, Inc.

Reason: Product is being recalled due to low pH value.
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product: 32 count Miss Vickies Multipack Box 44 oz. packaged in flexi…
Reason: Potential presence of Salmonella
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product: 30 count Lays Kettle Cooked Multipack Tray 41.25 oz. package…
Reason: Potential presence of Salmonella
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product: 30 count Miss Vickies Multipack Tray 41.25 oz. packaged in f…
Reason: Potential presence of Salmonella
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product: 20 count Frito-Lay Bold Mix Sack 18.4 oz. packaged in flexib…
Reason: Potential presence of Salmonella
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product: 12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged…
Reason: Potential presence of Salmonella
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product: Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape…
Reason: Potential presence of Salmonella
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Vertical Pharmaceuticals, Inc.

Product: Vertical Pharmaceuticals OB Complete with DHA Prenatal Multi…
Reason: One (1) lot (21511158) of the OB Complete DHA is being recalled because the label claim for "Omega-3 Fatty Acids" does not match the actual formulation.
Published: May 17, 2017
Distribution: AL, AR, AZ, CA, CO, FL, GA, IL, LA, MA,…

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FDA Recall United States Terminated Historical recordClass II

Treehouse Foods

Product: Macaroni & Cheese microwaveable cups sold under the followin…
Reason: Products containing cheddar cheese seasoning which may be contaminated with Salmonella.
Published: May 17, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Reser's Fine Foods, Inc.

Product: Reser's Fine Foods, American Classics Macaroni Salad, Net Wt…
Reason: Product contains undeclared milk and soy.
Published: May 17, 2017
Distribution: Product was distributed to wholesalers f…

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Data last updated: October 4, 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.