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Recall totals

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

37,450
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresh-ready-foods-llc-recalls-fresh-you-brand-sausage-egg-cheese-biscuit-sandwich-due-possiblePublished November 8, 2026
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 14,501–14,520 of 21,307 recalls

FDA Recall United States TerminatedTerminated: May 1, 2018Historical recordClass II

National Fish & Seafood, Inc.

Product
AMERICAS CHOICE B/D SHRIMP BEER BATTERED POPCORN 12/14 OZ
Reason
Product may contain undeclared milk.
Published
July 19, 2017
Distribution
CA CT FL GA IL IN MA MD ME MI…

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FDA Recall United States TerminatedTerminated: August 15, 2018Historical recordClass I

Wildway LLC

Product
Wildway Vanilla Bean Espresso Grain-free Granola 8 oz. UPC…
Reason
Potential to be contaminated with Listeria monocytogenes.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 15, 2018Historical recordClass I

Wildway LLC

Product
Wildway Coconut Cashew Grain-free Granola 8 oz. and 10 oz. U…
Reason
Potential to be contaminated with Listeria monocytogenes.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 15, 2018Historical recordClass I

Wildway LLC

Product
Wildway Banana Nut Grain-free Granola 8 oz. UPC: 85866000517…
Reason
Potential to be contaminated with Listeria monocytogenes.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 15, 2018Historical recordClass I

Wildway LLC

Product
Wildway Apple Cinnamon Grain-Free Granola 8 oz and 10 oz UPC…
Reason
Potential to be contaminated with Listeria monocytogenes.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2021Historical recordClass II

3CS ORGANICS LLC

Product
Topfer Lactana Bio 1 Anfangsmilch, 600g (3/case), Topfer Lac…
Reason
The product is not FDA approved and not all products are labeled in English.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2021Historical recordClass II

3CS ORGANICS LLC

Product
HOLLE Bio Zulgelingen Opvolgmelk 2, (3/case), HOLLE Bio Lait…
Reason
The product is not FDA approved and not all products are labeled in English.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2021Historical recordClass II

3CS ORGANICS LLC

Product
HIPP HA Combiotik HA 1, 500g (4/case), HIPP Combiotik HA 2,…
Reason
The product is not FDA approved and not all products are labeled in English.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 11, 2021Historical recordClass II

3CS ORGANICS LLC

Product
HIPP Bio Combiotik 1, Canister, 900g (4/case), HIPP Bio Co…
Reason
The product is not FDA approved and not all products are labeled in English.
Published
July 19, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 20, 2020Historical recordClass II

VenomX, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottles, Skin Protectant Phillips Company, Millerton, OK -- NDC 43074-207-01

by Phillips Co.

Reason
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 20, 2020Historical recordClass II

StaphWash+Plus+ Skin Protectant, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 43074-101-01

by Phillips Co.

Reason
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 20, 2020Historical recordClass II

StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 04307-100-11

by Phillips Co.

Reason
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 20, 2020Historical recordClass II

Diabecline brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-100-11

by Phillips Co.

Reason
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 20, 2020Historical recordClass II

TetraStem brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-301-11

by Phillips Co.

Reason
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: July 20, 2020Historical recordClass II

Tetracycline-ABC Brand Topical ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 4307410201

by Phillips Co.

Reason
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: June 12, 2018Historical recordClass II

Succinylcholine Chloride, 100 mg per 5mL, 20 mg per mL syringe. IV Use Only. JCB Laboratories, 8710 E 34th St., N. Wichita, KS 67226 UPC 7335968405

by Fagron Compounding Services LLC dba Fagron Sterile Services

Reason
Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial supplier
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: May 9, 2018Historical recordClass III

G & W Clobetasol Propionate Ointment 0.05%, packaged in a) 15 g tube (NDC 0713-0656-15), b) 30 g tube (NDC 0713-0656-31, c) 45 g tube (NDC 0713-0656-37), d) 60 g tube (NDC 0713-0656-60), Rx Only, Manufactured by G & W Laboratories, Inc. 111 Coolidge Street, South Plainfield, NJ 07080

by G & W Laboratories, Inc.

Reason
Failed impurities/degradation specifications: This product is being recalled due to out of specification results for Clobetasol Related Compound A, a known impurity which is a degradation product.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 7, 2020Historical recordClass II

parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and Antigingivitis Toothpaste, 0.454% (0.15% w/v fluoride ion), 3.4 OZ (96.4 g) tube, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059, NDC 0135-0601-01.

by GSK Consumer Healthcare

Reason
Presence of Foreign Substance: possibility of the presence of metal in the product.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 30, 2019Historical recordClass II

Clindamycin Injection USP; 900 mg/6 mL (150 mg/mL). 6 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-464-69

by Alvogen, Inc

Reason
Lack of Assurance of Sterility
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 30, 2019Historical recordClass II

Clindamycin Injection USP; 600 mg/4 mL (150 mg/mL). 4 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-463-69

by Alvogen, Inc

Reason
Lack of Assurance of Sterility
Published
July 12, 2017
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.

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