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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.

37,139
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026
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 12,021–12,040 of 20,519 recalls

FDA Recall Terminated Historical recordClass II

Acne Shave Post-Shave Moisturizer (salicylic acid), 0.5%, 3.3 FL OZ (98 mL) tube, Distributed by: United Exchange Corp., 17211 Valley View Blvd., Cerritos, CA 90703 USA, UPC 7 80707 73112 3.

by Shadow Holdings DBA Bocchi Labs

Reason
CGMP Deviations: products may be contaminated with bacteria.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g) bottles (UPC 8 50547 00503 3, Distributed by Herb-X Solutions, Inc., 3838 West Burbank Blvd., Burbank CA 91505.

by Shadow Holdings DBA Bocchi Labs

Reason
CGMP Deviations: products may be contaminated with bacteria.
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

READYFLUSH PROTECT with Dimethicone (3.2%), Flushable Personal Cleaning Cloths, 24-count flexible pack. Manufactured by Medline Industries, Inc. Mundelein, IL 60060 USA. NDC 53329-066-58.

by Medline Industries Inc (Northpoint Services)

Reason
Microbial Contamination of a Non-Sterile Product.
Published
June 20, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride, 1 mL Total Volume in 3 mL syringe, Rx, PharMEDium Services, LLC, Dayton, NJ

by PharMEDium Services, LLC

Reason
Superpotent and Subpotent
Published
June 20, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Gericare Iron Supplement Elixir Ferrous Sulfate 220 mg, packaged in 16 fl oz. (473 mL) bottles, Dist by: Gericare Pharmaceuticals Corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-709-16, UPC 57896709167

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 Terminated Historical recordClass II

Gericare Diocto Liquid (Docusate Sodium 50mg), 50 mg/5 mL, packaged in 16 FL OZ (473 mL) bottles, Dist by: Gericare Pharmaceuticals Corp. 1650 63rd Street, Brooklyn, NY 11204, NDC 57896-403-16, UPC 357896-403164,

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 Terminated Historical recordClass II

SDA Senna Syrup (Sennosides 8.8mg), packaged in 8 FL. OZ. (236 mL) bottles, Distributed by SDA Laboratories 280 Railroad Avenue, Greenwich CT 06830, NDC 66424-562-08, UPC 366424562082

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 Terminated Historical recordClass II

Geritrex Senna Syrup (sennosides 8.8mg), packaged in 8 FL OZ. (236 mL) bottle, Distributed by Geritrex, LLC 144 Kingsbridge Rd East Mt Vernon, NY 10550, 1-800-736-3437, NDC 54162-007-08, UPC 354162007088

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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical recordClass I

New Century Snacks LLC

Product
Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingr…
Reason
Firm was notified by customer that some bags of Tropical Trail mix contain Yogurt Trail mix and therefore do not declare milk, soy, wheat or cashews.
Published
June 20, 2018
Distribution
Alabama, Arizona, California, Colorado,…

View recall →

FDA Recall Terminated Historical 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 Terminated Historical 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 →

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.