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Recall totals

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

37,060

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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 9, 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 Ongoing Historical recordClass I

EGGS UNLIMITED LLC

Product: Big Y Brown Jumbo A 12ct Eggs; UPC: 018894319146 Simple Trut…
Reason: Firm received, repackaged eggs that are potentially contamination with Salmonella.
Published: November 12, 2025
Distribution: Product was distributed to 3 retail cons…

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: Publix Large Shrimp Peeled & Deveined Tail On 31/40, net wt.…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: Publix Extra Large Shrimp Easy to Peel Deveined 21/25, net w…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs.…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lb…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25, net…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 l…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs.…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt.…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product: Kroger Raw Colossal EZ Peel Shrimp, net wt. 2lbs., UPC 20011…
Reason: Shrimp may be contaminated with Cesium-137 (Cs-137).
Published: November 12, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Teasdale Foods, Inc.

Product: Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), UPC…
Reason: Undeclared allergen - milk
Published: November 12, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Teasdale Foods, Inc.

Product: Giant/Martin's Crunchy Taco Dinner Kit, Net Wt 9.4 OZ (266g)…
Reason: Undeclared allergen - milk
Published: November 12, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Eagle Spice and Extract Co., Inc.

Product: Eagle Spice Ground Ginger 16 oz.
Reason: Contains elevated levels of lead (Pb)
Published: November 12, 2025
Distribution: Multiple states

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FDA Recall Ongoing Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 30 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-048-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Published: November 5, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Desipramine Hydrochloride Tablets, USP, 75 mg, 100 count bottle (NDC 23155-581-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.

by Heritage Pharmaceuticals Inc

Reason: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Published: November 5, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 70 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-052-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Published: November 5, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-051-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Published: November 5, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 50 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-050-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Published: November 5, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 40 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-049-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Published: November 5, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 20 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-047-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.
Published: November 5, 2025
Distribution: Nationwide

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Data last updated: September 9, 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.