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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,113

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 15, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Lidocaine Cream, 4%, packaged in a) Net Wt. 15 grams tubes, NDC 52565-122-15; b) Net Wt. 30 grams tubes, NDC 52565-122-30; c) 5 x 5 gram tubes, NDC 52565-122-07; Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310; 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

Hydrocortisone Butyrate Lotion, 0.1%, packaged in a) 2 fl oz (59 mL) bottles, NDC 52565-087-02; b) 4 fl oz (118 mL) bottles, NDC 52565-087-04, 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

Halobetasol Propionate Ointment, 0.05%, Net Wt. 50 grams tube, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation, dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-998-67.

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

Hydrocortisone Butyrate Lotion 0.1%, 4 fl. oz. (118 mL) bottle, Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-159-04.

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

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FDA Recall Terminated Historical recordClass II

Halobetasol Propionate Ointment, 0.05%, packaged as a) 15 g tubes, NDC 52565-073-15; b) 50 g tubes, NDC 52565-073-51, 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

Halobetasol Propionate Ointment, 0.05%, Net Wt. 50 grams tube, Rx only, Manufactured for: SOLA Pharmaceuticals, Baton Rouge, LA 70809, NDC 70512-033-50.

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

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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

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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 →

Data last updated: September 15, 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.