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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 721–740 of 17,758 recalls

FDA Recall Ongoing 2026 recordClass II

LIQUID DAYQUIL 12/8oz

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

DAYQUIL COLD & FLU, 32CT/2PK

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Claritin, 20 Count, UPC: 655708016305

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Bayer 2Pk- 25 CT

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Benadryl, 25'S 2PK Box, UPC 815556020316

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Aleve 1's, 60 CT

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559

by GOLD STAR DISTRIBUTION INC

Reason
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each

by Encon Safety Products Co

Reason
cGMP deviations.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 47781-662-10.

by Alvogen, Inc

Reason
Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Clindamycin Phosphate USP, 1% (10 mg/mL), Topical Solution, 60 mL per applicator bottle, Rx only, Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel; Dist. by: Taro Pharmaceuticals USA, Inc., Hawthorne, NY 10532, NDC# 51672-4081-4

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Fluocinolone Acetonide Solution Topical Solution USP, 0.01%, 60-mL bottles, Rx only, Dist. by: Taro Pharmaceuticals Inc., Hawthorn, NY 10532. NDC 51672-1365-4

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Impurities/Degradation Specifications: Out of specification result was obtained for the known impurity D.
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass I

Herbs Forever

Product
HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Suppleme…
Reason
Potential undeclared allergen ingredient (Wheat)
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass I

Herbs Forever

Product
HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 V…
Reason
Potential undeclared allergen ingredient (Wheat)
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

AZ Gems, Inc.

Product
Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial…
Reason
elevated levels of chloramphenicol in frozen shrimp
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

WhiteWave - Louisville Pilot Plant

Product
So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, N…
Reason
Foreign material
Published
January 21, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Rosuvastatin Tablets, USP, 10 mg, Rx Only, 50 Tablets (5 x 10) Unit Dose per carton, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 50268-709-15

by AvKARE

Reason
Out of specification for dissolution.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887

by Medinatura New Mexico, inc.

Reason
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863

by Medinatura New Mexico, inc.

Reason
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Published
January 14, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0522-01. Case label: SpecGx LLC, NDC 0406052201, Exp. 2027/03, Lot: 0522J23493

by SpecGx, LLC

Reason
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Published
January 14, 2026
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.