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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 27, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass III

Imipramine HCl Tablets, USP, 25 mg, 100 count bottles, Mfd By: Mutual Pharmaceutical Co., Inc., Philadelphia, PA --- NDC 54738-913-01

by Mutual Pharmaceutical Company, Inc.

Reason: Chemical Contamination; benzophenone leached from the product label varnish
Published: September 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Imipramine HCl Tablets, USP, 10 mg, 100 count bottles, Rx only, Mfd By: Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 54738-912-01

by Mutual Pharmaceutical Company, Inc.

Reason: Chemical Contamination; benzophenone leached from the product label varnish
Published: September 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Felodipine Extended-Release Tablets, 10 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co Inc., Philadelphia, PA --- NDC 53489-370-01

by Mutual Pharmaceutical Company, Inc.

Reason: Chemical Contamination; benzophenone leached from the product label varnish
Published: September 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Felodipine Extended-Release Tablets, 5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-369-01

by Mutual Pharmaceutical Company, Inc.

Reason: Chemical Contamination; benzophenone leached from the product label varnish
Published: September 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Felodipine Extended-Release Tablets, 2.5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-368-01

by Mutual Pharmaceutical Company, Inc.

Reason: Chemical Contamination; benzophenone leached from the product label varnish
Published: September 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT), Packaged in a) 25 Drop Bags (UPC: 050428 448526) and b) 36 drop bags (UPC: 050428 476581), Over the Counter. Distributed by: CVS Pharmacy, Inc., One CVS Drive Woonsocket, RI 02895.

by Bestco, Inc.

Reason: Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey Lemon cough drops.
Published: September 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) Patient Preoperative Skin Preparation, supplied in a) 0.9 fl oz, 26 mL Single Use Applicator w/urethane sponge and 2-count Cotton-tipped swabs per pouch, packaged in 20 pouches per case (NDC 17518-0011-08, UPC (01) 0 03 17518 01108 5) and b) 0.2 fl oz, 6 mL Single Use Applicator w/urethane sponge per pouch, packaged in 50 pouches per case (NDC 17518-0011-07, UPC (01) 0 03 17518 01107 8), OTC, Made in U.S.A. by 3M Health Care, 2510 Conway Ave., St. Paul, MN 55144.

by 3M Company - Health Care Business

Reason: Chemical contamination: Product may be contaminated with a toxic compound.
Published: September 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lamivudine Oral Solution, USP, 10 mg per 1 mL, 240 mL bottle (8 ounces), Rx only, Manufactured by: Silarx Pharmaceuticals, Inc. Carmel, NY 10512, NDC 54838-0566-70

by Silarx Pharmaceutical, Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a customer complaint that the expiration date printed on the unit carton (5/18) does not match the expiration date on the bottle label (5/17).
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bi-Est (estriol,estradiol), Progesterone Vaginal Suppository, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bi-Est (estriol,estradiol), Progesterone, Testosterone cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bi-Est (estriol,estradiol) Testosterone cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estriol,Estradiol cream, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bi-Est (estriol,estradiol), Progesterone, DHEA, Testosterone drops, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol, Estriol capsules, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol, Estriol, Progesterone capsules, Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tri-Est 80:10:10 Progesterone (estriol, estradiol, estrone, progesterone) capsules Rx only, Manufactured by Park Compounding, Irvine, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811

by Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Reason: Failed Dissolution Specifications
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603-2116-28

by Qualitest Pharmaceuticals

Reason: Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
Published: September 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Methyl Folate Lyophilized Powder for Injection, 20 mg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA

by South Coast Specialty Compounding, Inc.

Reason: Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Published: September 9, 2015
Distribution: Nationwide

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Data last updated: September 27, 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.