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Recall totals

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

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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 2,072 recalls
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)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 5,041–5,060 of 21,324 recalls

FDA Recall United States Terminated Historical recordClass III

Dole Fresh Vegetables Inc

Product
Dole Chopped Kit Bacon & Bleu Green Cabbage, Green Leaf Lett…
Reason
Incorrect chemical added into wash systems when certain organic loads of vegetables start to create excessive foaming. The incorrect chemical added was a lot of foam detergent.
Published
January 18, 2023
Distribution
U.S. distribution to the following: AL,…

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FDA Recall United States Terminated Historical recordClass III

Dole Fresh Vegetables Inc

Product
Dole Very Veggie Green Leaf Lettuce, Iceberg Lettuce, Carrot…
Reason
Incorrect chemical added into wash systems when certain organic loads of vegetables start to create excessive foaming. The incorrect chemical added was a lot of foam detergent.
Published
January 18, 2023
Distribution
U.S. distribution to the following: AL,…

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FDA Recall United States Terminated Historical recordClass III

Dole Fresh Vegetables Inc

Product
Dole Chopped Kit BBQ Ranch Green Cabbage, Green Leaf Lettuce…
Reason
Incorrect chemical added into wash systems when certain organic loads of vegetables start to create excessive foaming. The incorrect chemical added was a lot of foam detergent.
Published
January 18, 2023
Distribution
U.S. distribution to the following: AL,…

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FDA Recall United States Terminated Historical recordClass II

Lidl US TRADING

Product
ACME Everything Bagel Smoked Salmon Net Wt. 4 OZ (113G) UPC:…
Reason
Possible pathogen grown and toxin formation in Salmon products
Published
January 18, 2023
Distribution
Distributed to stores in VA, MD, NC, GA,…

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FDA Recall United States Terminated Historical recordClass II

Lidl US TRADING

Product
ACME Smoked Nova Salmon Net Wt. 4 OZ (113G) UPC: 23384104065
Reason
Possible pathogen grown and toxin formation in Salmon products
Published
January 18, 2023
Distribution
Distributed to stores in VA, MD, NC, GA,…

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FDA Recall Terminated Historical recordClass II

Epi-Caine, Epinephrine 0.025% Lidocaine HCL 0.75% Solution for Intraocular Injection, 1 ml, Single Dose Vial, Compounded by Pine Pharmaceuticals, 355 Riverwalk Pkwy, Tonawanda, NY 14150. NDC 69194-0948-1

by Pine Pharmaceuticals, LLC

Reason
CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Published
January 11, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a) Case (NDC 0409-7620-59), b) Single Unit (NDC 0409-7620-49), Rx only, Distributed By Hospira, Inc., Lake Forest, IL 60045 USA,

by Pfizer Inc.

Reason
Lack of assurance of sterility: Bags have the potential to leak.
Published
January 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Prochlorperazine Maleate Tablets, USP 5mg, 100 tablets, RX Only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury, Maryland 21801, NDC 59746-113-06

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Subpotent Drug: Out of specification for assay at the 18-month stability timepoint.
Published
January 11, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd, E. Windsor, NJ 08520; Made in India. NDC 55150-155-20

by Eugia US LLC

Reason
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Published
January 11, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Mary's Gone Crackers

Product
Super Seed Everything Crackers 5.5 oz. UPC: 8 53665 00509 1
Reason
May contain foreign object: rubber pieces
Published
January 11, 2023
Distribution
Product was distributed to 8 distributor…

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FDA Recall United States Terminated Historical recordClass II

Mary's Gone Crackers

Product
Super Seed Classic Crackers (6 pk.) 5.5 oz. UPC: 8 97580 000…
Reason
May contain foreign object: rubber pieces
Published
January 11, 2023
Distribution
Product was distributed to 8 distributor…

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FDA Recall United States Terminated Historical recordClass I

Tai Phat Wholesalers LLC

Product
Three Gold Coins, Dried Mushrooms (01277) Nam Meo Nguyen T…
Reason
Products were found to be contaminated with Salmonella.
Published
January 11, 2023
Distribution
The product was distributed to consignee…

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FDA Recall United States Terminated Historical recordClass I

Tai Phat Wholesalers LLC

Product
Three Gold Coins, Dried Mushrooms (01052) Nam Meo Nguyen T…
Reason
Products were found to be contaminated with Salmonella.
Published
January 11, 2023
Distribution
The product was distributed to consignee…

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FDA Recall United States Terminated Historical recordClass I

Tai Phat Wholesalers LLC

Product
Three Gold Coins, Dried Mushrooms Sliced (01276) Nam Meo S…
Reason
Products were found to be contaminated with Salmonella.
Published
January 11, 2023
Distribution
The product was distributed to consignee…

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FDA Recall United States Terminated Historical recordClass I

Tai Phat Wholesalers LLC

Product
Three Gold Coins, Dried Mushrooms Sliced (01051) Nam Meo S…
Reason
Products were found to be contaminated with Salmonella.
Published
January 11, 2023
Distribution
The product was distributed to consignee…

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FDA Recall United States Terminated Historical recordClass I

Cranberry Sweets & More Inc

Product
Recalled Meltaways product is packaged in clear cellophane b…
Reason
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Published
January 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Timolol Maleate Ophthalmic Solution, USP 0.5%, 2.5 mL, Rx Only, Mfg by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Mfg for: Apotex Corp. Weston, FL 33326, NDC 60505-1005-4

by Apotex Corp.

Reason
Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.
Published
January 4, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Alcohol Antiseptic 80% Topical Solution Hand Sanitizer, Non-Sterile Solution, packaged as a a) 2.5 gallon bottle (9,464 ml), NDC 55533-524-02, and b) 55 gallon bottle (208,198 ml), NDC 55533-524-03, Manufactured for: Multi-Mist Products A Division of NCH Corporation 1618 Northgate, Irving, Texas 75062

by NCH Life Sciences LLC

Reason
CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.
Published
January 4, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Glycopyrrolate Tablets, USP, 1 mg, 50 Tablets (5x10) Unit Dose carton, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-363-15

by AVKARE LLC

Reason
Failed impurities/degradation specifications: Out of specification for unknown impurities.
Published
January 4, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ganciclovir for Injection, USP, 500mg per vial, packaged in a 10-count carton, Rx Only, Mfd. by: THYMOORGAN PHARMAZIE GmbH, Germany, Distributed by Hikma Berkeley Heights, NJ 07922, NDC 0143-9299-01

by Hikma Pharmaceuticals USA Inc.

Reason
Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.
Published
January 4, 2023
Distribution
Nationwide

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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.