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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,661–5,680 of 19,087 recalls

FDA Recall Terminated Historical recordClass II

Gentamicin Sulfate Ointment USP 0.1%, packaged as a) 15 grams tube, NDC 52565-090-15; b) 30 grams tube, NDC 52565-090-30, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Gentamicin Sulfate Cream USP, 0.1%, packaged in a) 15 g tubes, NDC 52565-085-15, b) 30 g tubes, NDC 52565-085-30, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fluocinonide Topical Solution USP, 0.05%, packaged in a) 20 mL bottles, NDC 52565-025-20; b) 60 mL bottles, NDC 52565-025-59, Rx only, Teligent Pharma, Inc., Buena, New Jersey 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fluocinonide Gel USP, 0.05%, packaged in a) 15 g tubes, NDC 52565-054-15; b) 60 g tubes, NDC 52565-054-60; c) 30 g tubes, NDC 52565-054-30, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fluocinonide Cream USP, 0.1%, 120 grams tube, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310, NDC 52565-079-11.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Econazole Nitrate Cream, 1%, packaged in a) 15 grams tubes, NDC 52565-022-15; b) 85 grams tubes, NDC 52565-022-85; c) 30 grams tubes, NDC 52565-022-30, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Diflorasone Diacetate Ointment USP, 0.05%, Net Wt 60 g tubes, Rx only, Manufactured for: SOLA Pharmaceuticals, LLC Baton Rouge, LA 70809, NDC 70512-031-60.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Diclofenac Sodium Topical Solution USP, 1.5% w/w, 5 fl. oz. (150 mL) bottles, Rx Only, Manufactured for: SOLA Pharmaceuticals, Baton Rouge, LA 70810, NDC 70512-025-05.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Diclofenac Sodium Topical Solution USP, 1.5% w/w, 5 fl. oz. (150 mL) bottle, Rx only, Teligent Pharma, Inc., Buena, New Jersey 08310, NDC 52565-002-05.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Desoximetasone Ointment USP, 0.25%, packaged in a) 100 grams tubes, NDC 52565-030-99; b) 60 grams tubes, NDC 52565-030-60; c) 15 grams tubes, NDC 52565-030-15, Rx Only, Teligent Pharma, Inc., Buena, New Jersey 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Desoximetasone Ointment USP, 0.05%, packaged in a) 100 grams tubes, NDC 52565-045-99; b) 60 grams tubes, NDC 52565-045-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Desoximetasone Ointment USP, 0.05%, Net Wt. 100 grams tubes, Rx only, Manufactured for: SOLA Pharmaceuticals, Baton Rouge, LA 70810, NDC 70512-037-10.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Desonide Ointment, 0.05%, packaged in a) 15 g tubes, NDC 52565-038-15; b) 60 g tubes, NDC 52565-038-60, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Gel, 0.05%, packaged in a) 15 grams tube, NDC 52565-082-15; b) 30 grams tube, NDC 52565-082-30; c) 60 grams tube, NDC 52565-082-60, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Ointment USP, 0.05%, packaged in a) 15 grams tube, NDC 52565-039-15; b) 30 grams tube, NDC 52565-039-30; c) 45 grams tube, NDC 52565-039-45; d) 60 grams tube, NDC 52565-039-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Lotion, 0.05%, packaged in a) 2 fl. oz. (59 mL) bottles, NDC 52565-055-02; b) 4 fl. oz. (118 mL) bottles, NDC 52565-055-04, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Cream USP, 0.05% (Emollient), packaged in a) 15 grams tube, NDC 52565-094-15; b) 30 grams tube, NDC 52565-094-30; c) 45 grams tube, NDC 52565-094-45; d) 60 grams tube, NDC 52565-094-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Clobetasol Propionate Cream USP, 0.05%, packaged in a) 15 grams tube, NDC 52565-051-15; b) 30 grams tube, NDC 52565-051-30; c) 45 grams tube, NDC 52565-051-45; d) 60 grams tube, NDC 52565-051-60; Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310

by Teligent Pharma, Inc.

Reason
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Published
March 30, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

REVITADERM WOUND CARE GEL, (Benzalkonium Chloride in a gel containing transforming growth factor-b), 0.1%, packaged in 29.6 mL (1.0 FL OZ) bottles (NDC 63347-120-02) and 88.7 mL (3.0 FL OZ) tubes (NDC 63347-120-01), Blaine Labs Inc., Santa Fe Springs, CA 90670

by Blaine Labs Inc

Reason
Microbial Contamination of Non-sterile Product; FDA analysis found the product to be contaminated with Bacillus cereus.
Published
March 30, 2022
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.