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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.

37,271
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 recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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 3,481–3,500 of 20,472 recalls

FDA Recall OngoingHistorical recordClass III

Tobramycin Opthalmic Solution USP, 0.3%, 5mL bottle, Rx only, Manufactured for: Alembic Pharmaceuticals, Bedminster, NJ 07921, USA, NDC 62332-518-05

by ALEMBIC PHARMACEUTICALS, INC.

Reason
Failed Impurities/Degradation Specifications
Published
August 23, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 12, 2024Historical recordClass III

PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61

by Advanced Accelerator Applications USA, Inc.

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Published
August 23, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 1, 2024Historical recordClass II

hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry 3-pack overwrap UPC 8 19156 02349 4, UPC 10819156023491 case; in the variety 3-pack of Strawberry + Unicorn + Grape UPC 8 19156 02332 6, UPC 10819156023323 case; and in a 24-count Toothpaste Floorstand, UPC 819156020684 (case).

by Colgate Palmolive Company

Reason
Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon fluoride free toothpaste.
Published
August 23, 2023
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Lett. Salad Shred Mix w/Rom, Produce Code 458009, 4-5 lb. b…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

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FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Lettuce Romaine All American, packaged in the following size…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

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FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Lettuce Rom Blend 50/50, packaged in the following sizes and…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

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FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Lett. Blend Rom/End/Rad-All Seasons packaged in the followin…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

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FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Lettuce Salad Blend Monterey, Produce Code 404709, 4-5lb. ba…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

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FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Romaine lettuce packaged into the following configurations a…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

View recall →

FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Lettuce Romaine 80/20 GB, packaged in the following sizes an…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

View recall →

FDA Recall United States OngoingHistorical recordClass II

G.O. Corporation

Product
Lettuce Mix w 20 Romaine, Produce Code 421009, 4-5 lb. bags…
Reason
Romaine lettuce may be contaminated with deer feces.
Published
August 23, 2023
Distribution
Multiple states

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FDA Recall TerminatedTerminated: February 26, 2024Historical recordClass III

Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T of D & NH), India, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512. NDC 47335-063-86

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Out of Specification result observed in content uniformity testing
Published
August 16, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: November 7, 2023Historical recordClass I

ONO LLC

Product
ONO Vegan Blueberry Muffin Protein Overnight Oats, 2.75oz. U…
Reason
Undeclared milk
Published
August 16, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: September 29, 2023Historical recordClass I

Cava Foods LLC

Product
Cava Spicy Hummus UPC 89832800227 Net Wt. 8oz./226.8 g Pack…
Reason
Undeclared sesame
Published
August 16, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: January 11, 2024Historical recordClass I

Betty Lou's Inc

Product
Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, C…
Reason
Undeclared sesame. Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds product containing sesame was packaged and labeled with Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds labels that did not declare sesame.
Published
August 16, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 21, 2025Historical recordClass II

PHENYLephrine in 0.9 sodium chloride, 400 mcg /10 mL, (40 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6007-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published
August 9, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 21, 2025Historical recordClass II

rocuronium, 50 mg /5 mL, (10 mg/mL), 5 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6010-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published
August 9, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 21, 2025Historical recordClass II

ePHEDrine in 0.9% sodium chloride, 50 mg /5 mL, (10 mg/mL), 5 mL Syringe, Rx only, CAPS Inc., Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-6004-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published
August 9, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 21, 2025Historical recordClass II

fentaNYL 2 mcg/mL and bupivacaine 0.125% PF in 0.9% sodium chloride / Total Volume = 250 mL, Total fentaNYL 500 mcg/250 mL, bag, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2082-2

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published
August 9, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 21, 2025Historical recordClass II

ketamine in 0.9% sodium chloride, 50 mg/5mL (10mg/mL), 5 mL syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-3022-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published
August 9, 2023
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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