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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 12, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

Refresco Beverages US Inc

Product: Great Value; 8oz Apple Juice in 6 pack; 100% Juice; packaged…
Reason: Product contains inorganic arsenic above action level set in industry guidance (13.2ppb)
Published: August 28, 2024
Distribution: Retail locations in: AL, CT, DC, DE, FL,…

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FDA Recall Ongoing Historical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, [NDC 64980-514-05].

by FDC Limited

Reason: Defective container; yellow colored spike from cap lodged in the nozzle
Published: August 21, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

North Fish USA, Inc.

Product: Cold Smoked Capelin, 9-ounce packages, plastic trays, 34 pac…
Reason: Clostridium botulinum (uneviscerated fish)
Published: August 21, 2024
Distribution: U.S. distribution to the following: GA a…

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FDA Recall United States Terminated Historical recordClass I

Foppen Paling En Zalm B.V.

Product: Foppen Smoked Norwegian Salmon Slices - Toast Size, packaged…
Reason: Potential contamination with Listeria monocytogenes
Published: August 21, 2024
Distribution: AL, AR, GA, IL, IN, KY, LA, MI, MO, MS,…

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FDA Recall United States Terminated Historical recordClass I

Publix Super Markets, Inc.

Product: Boars Head Grab and Go Wedge Ham, Smoke Master Black Forest…
Reason: Potential Listeria Monocytogenes
Published: August 21, 2024
Distribution: U.S. Distribution within the states in r…

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FDA Recall United States Terminated Historical recordClass II

G.S. Gelato and Desserts Inc.

Product: FULL CIRCLE market COCONUTMILK CHOCOLATE ALMOND CRUNCH NON0D…
Reason: Undeclared cashews. The firm was notified by a customer that the top label and the carton labels do not match. The carton label states, "coconut milk" while the top label states, "cashew milk". The product actually contains the cashew milk product.
Published: August 21, 2024
Distribution: The product was shipped to the following…

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FDA Recall Terminated Historical recordClass II

Gabapentin Tablets, USP, 600 mg, 500-count bottles, Rx only, Manufactured by: Granules India Limited Hyderabad-500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA NDC 70010-227-05

by Granules Pharmaceuticals Inc.

Reason: Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2

by A-S Medication Solutions LLC

Reason: Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064

by EMPOWER CLINIC SERVICES LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass III

Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only, Distributed By: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC# 69238-1423-1

by Amneal Pharmaceuticals, LLC

Reason: Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate Tablet USP 0.1 mg within the Methotrexate 2.5 mg 100-count Bottle.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PEG-3350, Sodium Sulfate, Sodium Chloride, Potassium Chloride, Sodium Ascorbate, and Ascorbic Acid for Oral Solution 100g/7.5 g /2.691 g/1.015 g/ 5.9 g / 4.7 g, 3 pouches/carton, Rx only, Distributed by: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC# 0093-3560-26.

by Novel Laboratories, Inc. d.b.a Lupin Somerset

Reason: Defective container: potential for non-sealed pouches which can lead to product leakage.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.

by MAIN PRODUCTS INC

Reason: Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Sevelamer Carbonate for Oral Suspension 0.8g packets, packaged in 90 packets per container, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India NDC 43598-478-90

by Dr. Reddy's Laboratories, Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Panaderia Guatemex

Product: Panaderia Guatemex - Gusano packaged in plastic bag
Reason: Undeclared Allergen - Soy
Published: August 14, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Panaderia Guatemex

Product: Panaderia Guatemex - Curenitos packaged in plastic bag
Reason: Undeclared Allergen - Soy
Published: August 14, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Panaderia Guatemex

Product: Panaderia Guatemex - Pegado packaged in plastic bag
Reason: Undeclared Allergen - Soy
Published: August 14, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Panaderia Guatemex

Product: Panaderia Guatemex - Churros packaged in plastic bag
Reason: Undeclared Allergen - Soy
Published: August 14, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Panaderia Guatemex

Product: Panaderia Guatemex - Besos packaged in plastic bag
Reason: Undeclared Allergen - Soy
Published: August 14, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Panaderia Guatemex

Product: Panaderia Guatemex - Liso packaged in plastic bag
Reason: Undeclared Allergen - Soy
Published: August 14, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Panaderia Guatemex

Product: Panaderia Guatemex - Corona packaged in plastic bag
Reason: Undeclared Allergen - Soy
Published: August 14, 2024
Distribution: Multiple states

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Data last updated: September 12, 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.