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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

36,950
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 841–860 of 18,483 recalls

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

FDA Recall Ongoing Historical recordClass II

Lisdexamfetamine Dimesylate Capsules, 10 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 57664-046-88.

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

View recall →

FDA Recall Ongoing Historical recordClass II

0.9% SODIUM CHLORIDE Injection, USP, 100 mL, Rx only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC 0990-7984-37

by Otsuka ICU Medical LLC

Reason
Lack of Assurance of Sterility: Potential for flexible container leaks.
Published
November 5, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Everolimus tablets 2.5 mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC# 49884-119-91

by ENDO USA, Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Published
November 5, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Everolimus tablets 10 mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC# 49884-128-91

by ENDO USA, Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Published
November 5, 2025
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass III

Everolimus tablets 7.5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC# 49884-127-91

by ENDO USA, Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Published
November 5, 2025
Distribution
Nationwide

View recall →

Data last updated:

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.