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Recall totals

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

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 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 November 10, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall TerminatedTerminated: June 18, 2018Historical recordClass II

Travoprost Ophthalmic Solution USP, 0.004%, a) 2.5 mL and b) 5 mL bottles, Rx only, FOR USE IN THE EYES ONLY, Made in India, Distributed by: Par Pharmaceutical Cos., Inc, Spring Valley, NY 10977

by Par Pharmaceutical, Inc.

Reason: Lack of Assurance of Sterility; damage to the internal portion of the dropper tip portion of the container
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: May 8, 2017Historical recordClass II

purely elizabeth.

Product: Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz,…
Reason: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 15, 2018Historical recordClass II

Island Soups Company Inc.

Product: ISLAND SOUPS, FISH SOUP, NET WT. 16 OZ (28.4G)
Reason: Possible contamination with Clostridium botulinum
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 15, 2018Historical recordClass II

Island Soups Company Inc.

Product: ISLAND SOUPS, RED PEAS SOUP, NET WT. 16 OZ (28.4G)
Reason: Possible contamination with Clostridium botulinum
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 15, 2018Historical recordClass II

Island Soups Company Inc.

Product: ISLAND SOUPS, RED PEAS SOUP NO MEAT, NET WT. 16 OZ (28.4G)
Reason: Possible contamination with Clostridium botulinum
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 15, 2018Historical recordClass II

Island Soups Company Inc.

Product: ISLAND SOUPS, GUNGO PEAS SOUP, NET WT. 16 OZ (28.4G)
Reason: Possible contamination with Clostridium botulinum
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 15, 2018Historical recordClass II

Island Soups Company Inc.

Product: ISLAND SOUPS, GUNGO PEAS SOUP NO MEAT, NET WT. 16 OZ (28.4G)
Reason: Possible contamination with Clostridium botulinum
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 15, 2018Historical recordClass II

Island Soups Company Inc.

Product: ISLAND SOUPS, MANNISH WATER, NET WT. 16 OZ (28.4G)
Reason: Possible contamination with Clostridium botulinum
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 20, 2017Historical recordClass II

Rosa Foods HQ

Product: Soylent Food Bars, Net Wt. 2.12 oz (60g), 12 pack.
Reason: Rosa Foods is recalling Soylent Bar because a number of their customers have experienced gastrointestinal issues after consuming Soylent Bars.
Published: December 7, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 26, 2017Historical recordClass II

Phenobarbital Tablets, USP 60mg 100=count bottles, Rx Only, Mfd. by: West-Ward Pharmaceutical Corp. Eatontown, NJ 07724, NDC 0143-1455-01

by West-Ward Pharmaceuticals Corp.

Reason: Failed Dissolution Specifications: Phenobarbital Tablets have an out of specification for dissolution at the 12 month stability time point
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 28, 2018Historical recordClass II

Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 60045, NDC 0409-4093-32

by Hospira Inc.

Reason: Lack of Assurance of Sterility: Complaints of broken tips on the ampules.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 10, 2019Historical recordClass II

Desoximetasone Ointment USP, 0.25%, a) 15 g tubes (NDC 61748-206-15 and b) 60 g tubes (NDC 61748-206-60, Marketed by Versapharm Inc., An Akorn Company, Lake Forest, IL, Manufactured by Hi-Tech, Pharmacal Co, Inc., Amityville, NY

by Akorn Inc

Reason: Failed Stability Specifications; out-of specification value for homogeneity / phase separation.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 1, 2017Historical recordClass III

Diltiazem HCl Extended-release Capsules, USP 120 mg, 100-count bottle (NDC 0378-5220-01), 500-count bottle (NDC 0378-5220-05), Rx Only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV, 26505 USA

by Mylan Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications: OOS results for known compound.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 1, 2020Historical recordClass II

LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620, NDC 60793-860-01

by Pfizer Inc.

Reason: Superpotent
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 12, 2018Historical recordClass III

BuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 300 mg, Rx Only, 500-count bottles, Manufactured by Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA inc. Pennington, NJ 08534, NDC 68382-354-05

by Zydus Pharmaceuticals USA Inc

Reason: Failed Dissolution Specifications: Product did not meet dissolution specification at an intermediate time point.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 20, 2017Historical recordClass III

KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g), 15 g bottle, Physician Sample: Not For Sale, Rx only, RANBAXY, Jacksonville, FL 32257, UPC 3 10631 09335 8.

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Stability Specifications: Low Out of Specification results for alcohol content.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass III

Amoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan, NDC 0143-9887-01

by West-Ward Pharmaceuticals Corp.

Reason: Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II

Lactulose Solution, USP, 10 g/15 mL, 15 mL unit dose cups (NDC 66689-039-01), packaged in 15 mL x 50 unit dose cups per case (NDC 66689-039-50), Rx only, Manufactured by VistaPharm, Inc., Largo, FL 33771.

by VistaPharm, Inc.

Reason: Microbial Contamination of Non-Sterile Products: bulk solution tested positive for the presence of the bacteria, Burkholderia cepacia.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 22, 2017Historical recordClass II

EN-R-G Foods, Inc.

Product: Protein Chews Juneberry,1.8oz, film package, 12 packets per…
Reason: EN-R-G Foods is recalling Cherry Lime Protein Chews, Raspberry Protein Chews, Juneberry Protein Chews due to complaints of nausea and/ or vomiting after consumption.
Published: November 30, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 22, 2017Historical recordClass II

EN-R-G Foods, Inc.

Product: Protein Chews Raspberry,1.8oz, film package, 12 packets per…
Reason: EN-R-G Foods is recalling Cherry Lime Protein Chews, Raspberry Protein Chews, Juneberry Protein Chews due to complaints of nausea and/ or vomiting after consumption.
Published: November 30, 2016
Distribution: Nationwide

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Data last updated: November 10, 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.