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 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.

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)

  • 1,527 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 13,021–13,040 of 20,519 recalls

FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Extra Large Seasoned/Battered Jo-Jo Wedges / 00148 (5 lb bag…
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Medium Seasoned/Battered Jo-Jo Wedges / 00129 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Seasoned/Battered Baby Jo-Jo Wedges / 00049 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Extra Large Coated Jo-Jo Wedges / 00048 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Battered Jo-Jo Wedges / 00047 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

Fresh Venture Foods, LLC

Product
Gold Coast Packing Broccoli Florets; packed in the follow…
Reason
Firm test results found potential E-coli contamination in Broccoli Florets
Published
August 30, 2017
Distribution
California, Colorado, Minnesota, Missour…

View recall →

FDA Recall United States Terminated Historical recordClass III

Grandma's Herbs

Product
"Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Die…
Reason
Grandmas Herbs Cholesterol has undeclared soy lecithin.
Published
August 30, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Commonwealth Dairy, Llc

Product
Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt, 5.…
Reason
Recalling Friendly Farms Key Lime Crunch Tilts because it may contain undeclared almond pieces.
Published
August 30, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Medium Coated Jo-Jo Wedges / 00040 (5lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

View recall →

FDA Recall Terminated Historical recordClass III

Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 50268-804-12

by AVKARE Inc.

Reason
Failed impurities/degradation specifications: Out of specification for a related compound C.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg) Tablets, wallet of 28 tablets (NDC 68180-911-11), Carton of 3 wallets (NDC 68180-911-13), Rx Only, Manufactured by: Lupin Limited, India, Distributed by Lupin Pharmaceuticals, Inc., Baltimore, MD, 21202

by Lupin Limited (Unit 1)

Reason
Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC: 700580499842

by Genetic Edge Compounds LLC

Reason
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: FDA analysis found the product to tainted with undeclared anabolic steroids and steroid like substances.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09

by ICU Medical Inc

Reason
Presence of Particulate Matter; stainless steel
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Halyard 24-Hour Oral Care Kit q4, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse. Manufactured by Halyard Health Inc., 5405 Windward Parkway, Alpharetta, GA 30004. Distributed by Halyard Sales, LLC Alpharetta, GA 30004. REF # 97014

by Akorn Inc

Reason
Crystallization with subpotent out of specification assay results for chlorhexidine.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Halyard 24-Hour Oral Care Kit q2, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse. Manufactured by Halyard Health Inc., 5405 Windward Parkway, Alpharetta, GA 30004. Distributed by Halyard Sales, LLC Alpharetta, GA 30004. REF # 97012

by Akorn Inc

Reason
Crystallization with subpotent out of specification assay results for chlorhexidine.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL Unit Dose Cup, a) unit dose cup (NDC 50383-720-15), b) 100-count tray (NDC 50383-720-19), Rx Only, Hi-Tech Pharmacal Co. Inc., Amityville, NY 11701.

by Akorn Inc

Reason
Crystallization with subpotent out of specification assay results for chlorhexidine.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004

by DYNAMIC TECHNICAL FORMULATIONS

Reason
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: Product was tested by FDA and found to contain andarine and ostarine.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations, UPC: 7 48252 86193 1

by HARDCORE FORMULATIONS

Reason
Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0

by HARDCORE FORMULATIONS

Reason
Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.
Published
August 23, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles (NDC 10702-026-10), Rx only, mfd. by: KVK-TECH, INC. NEWTOWN, PA 18940

by KVK-Tech, Inc.

Reason
Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test.
Published
August 23, 2017
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.