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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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

State: AK ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 14, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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FDA Recall United States Terminated Historical recordClass II

Pacific Coast Fruit Company

Product: Kit Thai Noodle Salad FM; Net weight 6.75 lbs. UPC 0-20728-7…
Reason: Thai Noodle Salad Kits is being recalled due to potential foreign material present in an ingredient.
Published: March 30, 2022
Distribution: Product was distributed to a distributor…

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FDA Recall Terminated Historical recordClass I

Avaphinal Maximum Male Enhancement Sexual Pills, 2000 MG*, packaged in 10 Capsules per carton.

by Walmart Stores

Reason: Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: March 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection USP, 250 mL Excel Container, Rx only, B. Braun Medical Inc., Bethlehem, PA, NDC 0264-7800-20

by B. Braun Medical, Inc.

Reason: Lack of sterility assurance: leaking bags
Published: March 23, 2022
Distribution: Nationwide

View recall →

Data last updated: September 14, 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.