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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 October 2026.

37,269
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 1,401–1,420 of 21,432 recalls

FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVING…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
Top Secret Nutrition extra strength uric control fast acting…
Reason
Unapproved Drug Claims.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SER…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVING…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK C…
Reason
Unapproved Drug Claims.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS…
Reason
Unapproved Drug Claims.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LO…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & CI…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC V…
Reason
Unapproved Drug Claims.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc He…
Reason
Unapproved Drug Claims.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS FISH OIL HEART AND BRAIN HEALTH EPA/…
Reason
Unapproved Drug Claims.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS BETA SITOSTEROL (715MG PINE DERIVED…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
HI-TECH PHARMACEUTICALS ADDEREX XR STRONGEST FOCUSING AID WI…
Reason
Unapproved Drug Claims and Misbranded.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: February 19, 2026Historical recordClass III

Hi-Tech Pharmaceuticals Inc.

Product
FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADR…
Reason
Unapproved Drug Claims.
Published
September 24, 2025
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Frozen AquaStar Breaded Shrimp, Butterfly, Clean-Tail, 16/20…
Reason
Product may be contaminated with Cesium-137 (Cs-137).
Published
September 24, 2025
Distribution
The affected AquaStar brand Cocktail Shr…

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FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
Frozen Mercado Kroger Cooked Shrimp - Medium - Peeled - Tail…
Reason
Product may be contaminated with Cesium-137 (Cs-137).
Published
September 24, 2025
Distribution
The affected AquaStar brand Cocktail Shr…

View recall →

FDA Recall United States OngoingHistorical recordClass II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product
AquaStar Cocktail Shrimp, 4oz. shrimp/2oz. cocktail sauce. E…
Reason
Product may be contaminated with Cesium-137 (Cs-137).
Published
September 24, 2025
Distribution
The affected AquaStar brand Cocktail Shr…

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FDA Recall OngoingHistorical recordClass II

chloroproMAZINE Hydrochloride Tablets, USP, 100 mg, 50 Tablets (5x10) unit dose carton, Rx only, Manufactured for: AvKare, Pulaski, TN, 38478, NDC 50268-165-15

by AvKARE

Reason
Presence of a foreign substance.
Published
September 17, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

chloroproMAZINE Hydrochloride Tablets, USP, 50 mg, 50 Tablets (5x10) unit dose carton, Rx only, Manufactured for: AvKare, Pulaski, TN, 38478, NDC 50268-164-15

by AvKARE

Reason
Presence of a foreign substance.
Published
September 17, 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.

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