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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 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
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026
Most affected stateHawaii 200 recalls mention this state

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Download matching recalls as CSV

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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)

  • 1,956 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 13,021–13,040 of 21,307 recalls

FDA Recall TerminatedTerminated: September 5, 2018Historical recordClass III

Fentanyl Transdermal System, 100 mcg/h, packaged in 5 pouch system (NDC 0591-3214-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3214-54.

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO) degradant exceeding the specification limits
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 5, 2018Historical recordClass III

Fentanyl Transdermal System. 75 mcg/h, packaged in 5 pouch system (NDC 0591-3213-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3213-54.

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO) degradant exceeding the specification limits
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 5, 2018Historical recordClass III

Fentanyl Transdermal System, 50 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3212-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3212-54.

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO) degradant exceeding the specification limits
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 5, 2018Historical recordClass III

Fentanyl Transdermal System. 25 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3198-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3198-54.

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO) degradant exceeding the specification limits
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: December 12, 2018Historical recordClass II

VELCADE (bortezomib) for injection, 3.5 mg/vial, Reconstitution Information, SUBCUTANEOUS INJECTION ONLY add 1.4 mL 0.9% Sodium Chloride to make 2.5 mg/ mL final concentration, INTRAVENOUS INJECTION ONLY add 3.5 mL Sodium Chloride to 1 mg/mL final concentration, Rx Only, Distributed by MILLENNIUM Pharmaceuticals, Inc., Cambridge, MA 02139-4234, NDC 63020-0049-01

by Millennium Pharmaceuticals Inc.

Reason
Defective Container: Confirmed reports of loose vial crimps.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: March 17, 2020Historical recordClass I

Pantoprazole Sodium for Injection, 40 mg per vial, single dose vial, Rx only, Manufactured in India for: AuroMedics Pharma LLC, 6 Wheeling ROad, Dayton, NJ 08810. NDC 55150-202-00

by AuroMedics Pharma LLC

Reason
Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) contained a piece of glass
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 10, 2019Historical recordClass I

Ampicillin and Sulbactam for Injection 1.5 g vial, sterile Dry Powder for injection, 10 vials per carton, Distributed by AuroMedics Pharma LLC. 279 Princeton-Highstown Rd. E. Windsor, NJ 08520, NDC 55150-116-20

by Aurobindo Pharma Ltd.

Reason
Presence of Particulate Matter: A confirmed customer report was received for the presence of visible particulate matter, confirmed as glass, within a single vial.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: November 24, 2020Historical recordClass III

Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups), Rx Only, Dist. By McKesson Packaging Services a business unit of McKesson Corporation 7101 Weddington Rd. Concord, NC 28027, NDC 63739-549-51

by Mckesson Packaging Services

Reason
Subpotent Drug: Out of specification for assay (stability testing)
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

TAD Glutathione Whitening Kits lyophilized powder for injection, 600 mg vials, 10 vials + 10 amps x 4 mL, Manufactured by: Biomedica Foscama Industria, Ferentino, Italy

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Saluta Glutathione Whitening kits, packaged in 600 mg, 1200 mg and 1800 mg glass vials, Manufactured by: Shandong Luye Pharmaceutical Co, Ltd, Yantai, Shandong. PRC

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Ling Zhi capsules

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Sterilized water for injections BP, 50 x 5 mL plastic ampules, Manufactured in India

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

TP Drug Laboratories Vitamin C ampules

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Reiki Glutathione Whitening kits

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Laennec INJ, Placenta extract (human), 2mL vials, Manufactured by: GCJBP Corp, Korea

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Tationil Glutathione, 600 mg/ 4 mL, polvere e solvente per soluzione iniettabile, Teofarma, s.r.l.

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Laroscorbine Platinum Vitamin C 1 gm Collagen 0.35 gm, Roche

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Relumins Vitamin C Solvent ampules

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 13, 2018Historical recordClass II

Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials

by Flawless Beauty LLC

Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Published
February 14, 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.

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