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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: MP ×
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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

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 I

SunOpta Grains and Foods Inc.

Product: Good & Gather Organic cherries & berries fruit blend. Blueb…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Cherries packaged under the following brands and sizes: 1.…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

SunOpta Grains and Foods Inc.

Product: 365 Whole Foods Market Organic Blackberries. Net Wt 10 oz (…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Good & Gather Blueberries. Net Wt 48 oz (3lb) 1.36kg UPC…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

SunOpta Grains and Foods Inc.

Product: 365 Whole Foods Market Organic Whole Strawberries. Net Wt…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Mango Chunks packaged under the following brand names and si…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

SunOpta Grains and Foods Inc.

Product: Pineapple Chunks packaged under the following brand names an…
Reason: Fruit products have the potential to be contaminated with Listeria monocytogenes.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Scenic Fruit Company, LLC

Product: Cadia - Organic Pineapple Frozen Fruit, packaged in stand-up…
Reason: Potential for contamination with Listeria monocytogenes. Pineapples are recalled by supplier Sunrise Growers Inc.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Scenic Fruit Company, LLC

Product: Trader Joe s Organic Tropical Fruit Blend Pineapple, Banana,…
Reason: Potential for contamination with Listeria monocytogenes. Pineapples are recalled by supplier Sunrise Growers Inc.
Published: July 26, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered Inhalation, net content 6.7 g canister packaged in a box, Rx only, Manufactured by: Cipla Ltd, Indore SE Z, Pithampur, India, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ, 07059, NDC 69097-142-60

by Cipla USA, Inc.

Reason: Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.

by Global Pharma Healthcare Private Limited

Reason: CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be contaminated.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.

by Global Pharma Healthcare Private Limited

Reason: Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.

by Global Pharma Healthcare Private Limited

Reason: CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be contaminated.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.

by Global Pharma Healthcare Private Limited

Reason: Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bivalirudin for Injection 250 mg, 10 Single-Dose Vials, Rx Only, Manufactured for: Accord Healthcare, Inc. Durham, NC 27703 Manufactured by: Intas Pharmaceuticals Limited Ahmedabad-382 210, India, NDC 16729-275-67.

by ACCORD HEALTHCARE, INC.

Reason: Presence of Particulate Matter: Particulate matter identified as fiber.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Atropine Sulfate Injection, USP 8 mg per 20 mL (0.4 mg per mL), 20 mL Multiple Dose Vials, Rx only, Manufactured for: Accord Healthcare, Inc. Durham, NC 27703 Manufactured by: Intas Pharmaceuticals Limited Ahmedabad-382 210, India, NDC 16729-512-43.

by ACCORD HEALTHCARE, INC.

Reason: Presence of Particulate Matter: Particulate matter identified as fiber.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA, NDC 0264-5802-00

by B. Braun Medical Inc.

Reason: Lack of assurance of sterility: bags have the potential to leak.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tiagabine Hydrochloride Tablets, 2 mg, 30-count bottle, Distributed by Sun Pharmaceutical Industries. Inc. Cranbury NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited Halol-Baroda Highway, Halol-389 350, Gujarat, India. NDC#: 62756-200-83

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Impurities: Out of Specification (OOS) result observed during Related Substances testing
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sunitinib Malate Capsules, 12.5 mg, 28-count bottles, Rx only, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0093-8199-28

by Teva Pharmaceuticals USA Inc

Reason: Failed Moisture Limits: Water (moisture) content above the approved product specifications.
Published: July 19, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 36800-691-39), b)45-count cartons (NDC 36800-691-95), and 90-count cartons (NDC 36800-691-75), Distributed by: Topco Associates LLC, Elk Grove Village, IL 60007.

by L. Perrigo Company

Reason: Failed Impurities/Degradation Specifications
Published: July 19, 2023
Distribution: Nationwide

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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.