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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

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 17, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass II

bevacizumab (Avastin) Injection, 1.25mg/0.05mL (0.12 mL Fill), Sterile Single-Dose Syringe, Fagron Sterile Services, 8710 E 34th St N. Wichita, KS 67226

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility
Published: September 24, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only, Manufactured by: Alken Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-432-03

by Ascend Laboratories, LLC

Reason: Superpotent drug
Published: September 24, 2025
Distribution: Nationwide

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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: 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: 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…

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Data last updated: October 17, 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.