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 October 2026.

37,447

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/vitality-works-inc-recalls-365-whole-foods-market-ashwagandha-capsules-sold-nationwide-due-potentialPublished October 30, 2026

Most affected stateHawaii 200 recalls mention this state

State: NE ×
Clear all

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

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated November 3, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Download CSV

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: October 21, 2026Historical recordClass I

World Variety Produce Inc dba Melissa's

Product: Organic Marketside Zucchini 2 Count packages/8 per case In…
Reason: Product may be contaminated with Salmonella
Published: May 4, 2022
Distribution: Product shipped to Walmart DC's in Arizo…

View recall →

FDA Recall TerminatedTerminated: July 31, 2024Historical recordClass II

artnaturals Hand Sanitizer

by VIRGIN SCENT INC

Reason: CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: July 31, 2024Historical recordClass I

artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5

by VIRGIN SCENT INC

Reason: Chemical Contamination: presence of benzene, acetaldehyde, and acetal.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 5, 2023Historical recordClass II

LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA

by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 5, 2023Historical recordClass II

BPC-157 2 mg/mL (5 mL) Injection, 5 mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081

by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: July 31, 2024Historical recordClass I

Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.

by Pink Toyz

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: July 31, 2024Historical recordClass II

artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5

by VIRGIN SCENT INC

Reason: CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 5, 2023Historical recordClass II

Sermorelin Acetate 1 mg/mL (6 mL) Injection, 6 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081

by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 5, 2023Historical recordClass II

PT-141 (Bremelanotide Acetate) 10 mg/mL (2 mL) Injection, 2mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081

by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 5, 2023Historical recordClass II

Melanotan II 1 mg/mL (10 mL) Injection, 10mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA

by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 5, 2023Historical recordClass II

Ipamorelin Acetate/Sermorelin Acetate (1 mg/1 mg)/mL (10 mL) Injection, 10 mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081

by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 5, 2023Historical recordClass II

ARA-290 (Cibinetide Acetate) 6 mg/mL (4 mL) Injection, 4 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA

by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: May 23, 2023Historical recordClass II

Rifampin for Injection, USP, 600 mg/vial, One Vial per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., NDC 67457-445-60

by MYLAN PHARMACEUTICALS INC

Reason: Failed Impurities/Degradation Specifications: High out of specification results obtained for related compound during stability testing.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 25, 2023Historical recordClass II

Diclofenac Sodium Topical Solution 1.5% w/w, Generic for Pennsaid, 150 ml bottle, Rx Only, Mfg: Sola Pharmaceutical, Preferred Pharmaceuticals, Inc., The Physicians Solutions, NDC 68788-7918-01

by Preferred Pharmaceuticals, Inc.

Reason: CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc. is discontinuing its stability study program.
Published: April 27, 2022
Distribution: Nationwide

View recall →

FDA Recall United States TerminatedTerminated: November 3, 2022Historical recordClass I

Liberty Fruit Co Inc DBA Carol's Cuts

Product: Carol's Cuts Fruit Medley Ingredients may include Honey, can…
Reason: Fresh-cut cantaloupe positive for Salmonella.
Published: April 27, 2022
Distribution: Distributed to retail and military groce…

View recall →

FDA Recall United States TerminatedTerminated: November 3, 2022Historical recordClass I

Liberty Fruit Co Inc DBA Carol's Cuts

Product: Carol's Cuts Fruit Tray Ingredients may include Honeydew, ca…
Reason: Fresh-cut cantaloupe positive for Salmonella.
Published: April 27, 2022
Distribution: Distributed to retail and military groce…

View recall →

FDA Recall United States TerminatedTerminated: November 3, 2022Historical recordClass I

Liberty Fruit Co Inc DBA Carol's Cuts

Product: Carol's Cuts Hawaiian Blend Ingredients may include Honeydew…
Reason: Fresh-cut cantaloupe positive for Salmonella.
Published: April 27, 2022
Distribution: Distributed to retail and military groce…

View recall →

FDA Recall United States TerminatedTerminated: November 3, 2022Historical recordClass I

Liberty Fruit Co Inc DBA Carol's Cuts

Product: Carol's Cuts Cantaloupe Chunks Ingredients may include cant…
Reason: Fresh-cut cantaloupe positive for Salmonella.
Published: April 27, 2022
Distribution: Distributed to retail and military groce…

View recall →

FDA Recall OngoingHistorical recordNot Yet Classified

Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036

by Centric Compounding LLC

Reason: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Published: April 20, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: May 10, 2022Historical recordClass II

Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid, 90-Count Bottle, Manufacturer: Dr Reddy's Laboratories Limited, NDC 68788-6390-09

by Preferred Pharmaceuticals, Inc.

Reason: Out of specification results observed in dissolution during long term stability testing.
Published: April 20, 2022
Distribution: Nationwide

View recall →

Data last updated: November 3, 2026 ET

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.