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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 11,041–11,060 of 23,216 recalls

FDA Recall United States Terminated Historical recordClass I

Rong Shing Trading NY Inc

Product
Glam Day Nougat Candy packaged in 6-ounce (170g) plastic pac…
Reason
Product may contain undeclared allergens, specifically milk and eggs.
Published
November 6, 2019
Distribution
Retailers in 17 states: CO, FL, GA, IL,…

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FDA Recall United States Terminated Historical recordClass II

Rong Shing Trading Inc.

Product
GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard…
Reason
Product contains undeclared milk
Published
November 6, 2019
Distribution
Retailer in 7 states: KY, MD, NY, UT, VA…

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FDA Recall Terminated Historical recordClass II

Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20

by Avella of Deer Valley, Inc. Store 38

Reason
Lack of sterility assurance.
Published
October 30, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-984-10

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason
Lack of Assurance of Sterility; bags have potential to leak
Published
October 30, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl; 25 g L-Lysine HCl, Single Dose Container, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-988-10

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason
Lack of Assurance of Sterility; bags have potential to leak
Published
October 30, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Sodium Chloride Injection-200 mL Total Dose: (400 mcg/200 mg)/200 mL, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-526-20

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason
GMP Deviations: potential glass contamination
Published
October 30, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride Injection-250 mL, Rx Only Total Dose: (500 mcg/312.5 mg)/250 mL, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-530-25

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason
GMP Deviations: potential glass contamination
Published
October 30, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Sodium Chloride Injection-250 mL Total Dose: (500 mcg/156.3 mg)/250 mL, Rx Only, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC 69374-0525-25

by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Reason
GMP Deviations: potential glass contamination
Published
October 30, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
Consider Bardwell Farm Dorset cheese PLU code 97776 sliced a…
Reason
Potential to contain Listeria monocytogenes
Published
October 30, 2019
Distribution
NORTH ATLANTIC AND NORTHEAST WHOLE FOODS…

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FDA Recall United States Terminated Historical recordClass II

The Newark Nut Store

Product
Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) ret…
Reason
Kopper s Chocolate has initiated recall of Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) retail package, metallized foil resealable pouch, 12 pouches per case, printed BB: 08/2020 because the product packaging only identifies soy as an allergen. The product does not list milk , which is an allergen .
Published
October 30, 2019
Distribution
The product was distributed to NY, NJ, a…

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FDA Recall United States Terminated Historical recordClass I

Euphoria Fancy Food Inc

Product
Capitan K Salmon slightly salted piece - net.wt 1.05 oz (200…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
October 30, 2019
Distribution
Product was distributed in NY, PA, NJ &…

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FDA Recall United States Terminated Historical recordClass I

Mrs. Stratton's Salads, Inc

Product
Tuna salad under the following brand names: BALLARDS FARM Ba…
Reason
Potential contamination from Listeria monocytogenes.
Published
October 30, 2019
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

Threshold Enterprises Ltd

Product
Source Naturals Dietary Supplement Brain Charge Advanced…
Reason
Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.
Published
October 30, 2019
Distribution
U.S. distribution to the following: AL,…

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FDA Recall United States Terminated Historical recordClass II

Wismettac Asian Foods, INC

Product
Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration…
Reason
Product label identifies bonito, but product dipping sauce actually contains skipjack tuna, yellowfin tuna, and bluefin tuna as well as does not state the general allergen name of fish.
Published
October 30, 2019
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Roland Foods, LLC

Product
Roland Brand Red Caviar - Whole Grain Lumpfish (Lumpfish Roe…
Reason
Potential to be contaminated with Clostridium botulinum.
Published
October 30, 2019
Distribution
Products were distributed in US states:…

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FDA Recall United States Terminated Historical recordClass I

Roland Foods, LLC

Product
Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish R…
Reason
Potential to be contaminated with Clostridium botulinum.
Published
October 30, 2019
Distribution
Products were distributed in US states:…

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FDA Recall United States Terminated Historical recordClass I

AMPLE HILLS MANUFACTURING

Product
Ample Hills Peppermint Pattie ice cream packed in 3 gallon t…
Reason
Product may contain undeclared peanut allergen
Published
October 30, 2019
Distribution
Distributed in NY, NJ, CA, FL

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FDA Recall United States Terminated Historical recordClass II

The Truck Farm, LLC

Product
Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix.…
Reason
The product contains wheat flour, but does not declare wheat on the label.
Published
October 30, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose Vial NDC 50742-464-50 Rx Only Ingenus Pharmaceuticals, LLC. Orlando, FL 32839

by Ingenus Pharmaceuticals Llc

Reason
Crystallization: Presence of particulate matter identified as API crystallization
Published
October 23, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Dextroamphetamine Sacharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, Mixed Salts of a single Entity Amphetamine Product), 20mg, 100-count bottle, RX Only, Distributed by: Aurobindo Pharma USA Inc., Dayton, NJ 08810, NDC 13107-073-01

by Aurobindo Pharma USA Inc.

Reason
Superpotent Drug: Amphetamine Mixed Salts 20mg have been found to be out of specification for weight and thickness.
Published
October 23, 2019
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.