Skip to main content

Data Explorer

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 November 2026.

37,449
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
Most affected stateHawaii 200 recalls mention this state

Advertisement

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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 12,541–12,560 of 21,307 recalls

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

Ritussin DM Dextromethorphan Hydrobormide (Dextromethorphan HBr, USP 10 mg, Guaifenesin, USP 100mg), packaged in 4 FL.OZ. (118 mL), RIJ PHARMACEUTICAL CORPORATION 40 COMMERCIAL AVENUE, MIDDLETOWN, NY 10941, NDC 5380740904, UPC 35380740941

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

GeriCare Senna Syrup (Sennosides 8.8 mg), 8 fl oz (237 mL) bottles, Dist, by Gericare Pharmaceuticals 1650 63rd Street Brooklyn, NY 11204, NDC 57696-452-08, UPC 357896452087

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

RPC APAP Elixir (Acetaminophen 160mg), Packaged in 16 FL. OZ. (473 mL) bottles, RIJ PHARMACEUTICAL CORPORATION, 40 COMMERCIAL AVENUE, MIDDLETOWN, NY, NDC 53807-129-16, UPC 353807129161

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

Gericare Liquid Pain Relief Acetaminophen Cherry Flavor 160mg/5mL, packaged in 16 FL OZ (473 mL), Dist. By Gericare Pharmaceuticals 1650 63rd Street Brooklyn, NY 11204, NDC 5789618016, UPC 357896180164

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

RPC Children's Non-Aspirin (Acetaminophen 160 mg) Elixir, packaged in 4 FL. OZ. (118 mL), RIJ PHARMACETUICAL CORPORATION, 40 COMMERCIAL AVENUE, MIDDLETOWN, NY 10941, NDC 53807-129-04, UPC 353807129048

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

RPC Senna Syrup (Sennosides 8.8mg), packaged in 8 fl oz (237 mL) bottles, RIJ Pharmaceuticals Corporation 40 Commercial Avenue, Middletown, NJ 10941, NDC 5380755608, UPC 353807556080

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

Preferred Plus Pharmacy Antacid (Aluminum Hydroxide 200mg, Magnesium Hydroxide 200mg Simethicone 20mg, packaged in 12 FL. OZ. (355 mL) bottles, Manufactured By: RIJ PHARMACEUTICAL CORPORATION 40 Commercial Avenue Middletown, NY 10941, Distributed by: Kinray Inc. Whitestone, NY 11357, NDC 53807-12612, UPC 53807126122

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 7, 2023Historical recordClass II

Preferred Plus Pharmacy Antacid Extra Strength (Aluminum Hydroxide 400mg, Magnesium Hydroxide 400mg, Simethicone 40 mg), packaged in 12 FL. OZ. (355 mL), Manufactured By: RIJ Pharmaceutical Corp.40 Commercial Avenue, Middletown, NY 10941, Distributed by: Kinray Inc. Whitestone, NY 11357 NDC 53807-158-12, UPC 353807158123

by RIJ Pharmaceutical LLC

Reason
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published
June 20, 2018
Distribution
Nationwide

View recall →

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

Divvies LLC

Product
simply delicious Divvies SEMI-SWEET PEPPERMINT BARS made to…
Reason
Product may contain traces of milk.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 1, 2021Historical recordClass II

R.A.B. Food Group LLC

Product
Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.2…
Reason
The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark, NJ 07105 has initiated a recall of Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz. /12 per case. because of an undeclared allergen peanut, tree nut and milk.
Published
June 20, 2018
Distribution
Distribution states  MD, PA, WA, CT, NY…

View recall →

FDA Recall TerminatedTerminated: March 27, 2020Historical recordClass I

Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use cartridge syringe, Single unit (NDC 0409-1782-03) and 10 count box (NDC 0409-1782-69), Rx Only, Hospira Inc., Lake Forest, IL

by HOSPIRA INC, LAKE FOREST

Reason
Presence of Particulate Matter; Potential for particulate matter on the syringe plunger.
Published
June 13, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: January 13, 2020Historical recordClass III

Nystatin Oral Suspension, USP, 500,000 units/5 mL, For Institutional Use Only, packaged in 5 mL cups, Rx Only, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-4810-05

by Pharmaceutical Associates Inc

Reason
Resuspension problems: Out of specification for appearance and resuspendability.
Published
June 13, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass II

Fluticasone propionate Nasal Spray, USP, 50 mcg, packaged in 50 mcg per spray 120 Metered Sprays bottles, 16 g net fill weight, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, FL 33326, NDC 60505-0829-1

by Apotex Inc.

Reason
Presence of foreign substance: glass particles
Published
June 13, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: March 29, 2019Historical recordClass I

Desly International Corp.

Product
Melanie Mini Cookies with Caramel Flavor in a 17.6 oz (500g)…
Reason
Products contain undeclared peanuts.
Published
June 13, 2018
Distribution
CA CT FL GA IL KS KY MA MD ME…

View recall →

FDA Recall United States TerminatedTerminated: March 29, 2019Historical recordClass I

Desly International Corp.

Product
Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plast…
Reason
Products contain undeclared peanuts.
Published
June 13, 2018
Distribution
CA CT FL GA IL KS KY MA MD ME…

View recall →

FDA Recall United States TerminatedTerminated: October 11, 2018Historical recordClass I

BLM Products U. Vertriebsges

Product
Priano Rosso Pesto Sauce, 6.7oz glass jar
Reason
BLM Prod.-und Vertriebsges.mbH & Co. KG has initiated a voluntary recall of Priano Rosso Pesto Sauce, 6.7 oz. packaged in glass jars due to undeclared allergens egg and milk.
Published
June 13, 2018
Distribution
Domestic only: Arkansas, California, Con…

View recall →

FDA Recall United States TerminatedTerminated: October 16, 2018Historical recordClass II

Dean Foods, Inc.

Product
Baskin Robbins Mint Chocolate Chip
Reason
Product may contain unlabeled coconut.
Published
June 13, 2018
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: July 2, 2018Historical recordClass II

Trader Joes Company

Product
Trader Joe's Artisan Bread - Organic French Baguette; (Bro…
Reason
FDA was notified by the Canadian Food Inspection Agency of that two lot codes of Trader Joe's Organic French Baguette may be contaminated with Listeria monocytogenes.
Published
June 13, 2018
Distribution
Distribution Centers in CA and PA - reta…

View recall →

FDA Recall United States TerminatedTerminated: May 20, 2019Historical recordClass I

Lake Michigan Distilling Co LLC

Product
Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, M…
Reason
Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a voluntary recall of Ethanol Extraction s 190 Proof Non-Denatured Grain Alcohol due to contamination with methanol which could cause serious injury or death if consumed.
Published
June 13, 2018
Distribution
Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…

View recall →

FDA Recall United States TerminatedTerminated: July 23, 2021Historical recordClass II

Ahold Usa

Product
Broccoli cuts, All Natural, No Preservatives, Net Wt 16 OZ;…
Reason
Ahold Delhaize received a report from State of CT of finding significant amount of Listeria monocytogenes in a bag of Stop and Shop's Broccoli Cuts, 16 oz.
Published
June 13, 2018
Distribution
CT, DC, MD, MA, NJ, NY PA, RI, VA and WV

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.

Reconnecting to the server…

We lost the connection to the server.

Your session has expired.