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Recall totals

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

37,139

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 25, 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 II

BLEACHING CREAM 0.1% CREAM, BLEACHING CREAM HQ4%, BLEACHING CREAM-NO HQ, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BL 20%/4% CREAM, BLT 20%/6%/4% CREAM, BLT 20%/6%/6%, BLT 20% 8% 4% CREAM, BLT 20% 8% 4% OINTMENT, BLT 20% 8% 6% CREAM, BLT 20%/ 8% /8% OINTMENT, BLT 20%/ 8% /8% CREAM, BLT 20%/ 7%/ 7% CREAM, BLT 20%/ 10%/ 4% CREAM, BLT 20%/ 10%/ 10% CREAM, BLT 20%/ 20%/ 10% OINTMENT,BLT 7%/ 10%/ 7% CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BENZOYL PEROXIDE 5% CLINDAMYCIN 1.2%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ADAPALENE 0.1%, BENZOYL PEROXIDE 2.5% GEL, ADAPELENE 0.3%, BENZOYL PEROXIDE 2,5% GEL, AZELAIC ACID 15% CREAM, AZELAIC ACID 20% IN OI FREE CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BICARBONATE 10%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MINOXADIL all strength including 2%, 5% and MINOXIDIL / RETINOIC ACID 5% / 0.025, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

5-FLUOROURACIL IN VANICREAM, FLUOROURACIL in all strengths including 0.05%, 5% CREAM, FLUOROURACIL 4.9% IN CERAVE CREAM, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

TACROLIMUS 0.1% Ointment and TACROLIMUS 0.1%/KETOCONAZOLE 2%, Rx only, Synergy Rx, 4901 Morena Blvd #504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

KETOCONAZOLE 2%/HYDROCORTISONE 1.5% CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676.

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HCG and HCG with resveratrol Human Chorionic Gonadotropin in different strengths: HCG 300 UNITS/RESVERATROL 50MG S.L. Tablet, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

CANTHARADIN 0.7% SOLUTION and CANTHARIDAN / PODOPHYLLUM SOLUTION, CANTHARIDIN/PODOPHYLLUM RESIN MIXTURE, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Human Chorionic Gonadotropin (HCG) 5,000 units/vial and 11,000 units/vial, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason: Lack of Assurance of Sterility: There are also CGMP Deviations.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT, 3.4 FL OZ (100 mL), Colgate Oral Pharmaceuticals, Inc., New York, NY 10022 --- NDC 0126-0016-61, UPC 3834110622

by Colgate Palmolive Co

Reason: Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GlipiZIDE Extended-release tablets, 2.5 mg, 30-count carton (NDC 68084-295-21), Individual dose (NDC 68084-395-11), Rx Only, Packaged and Distributed by American Health Packaging, Columbus, Ohio 43217, NDC 68084-295-21

by Amerisource Health Services

Reason: Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded dissolution specification rates for the 10 hour testing point.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clindamycin Phosphate Topical Solution USP, 1%, packaged in a) 30 mL applicator bottles (NDC 0472-0987-91) and b) 60 mL applicator bottles (NDC 0472-0987-92), Rx Only, Manufactured by: G&W Laboratories, Inc., 111 Coolidge Street, South Plainfield, NJ 07080; Distributed by: Actavis Mid Atlantic LLC, 1877 Kawai Road, Lincolnton, NC 28092.

by G & W Laboratories, Inc.

Reason: CGMP Deviations: an expired active ingredient was used in the manufacture of these recalled lots.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection, Preservative Free, Rx only, Compounded by Isomeric Pharmacy Solutions, Salt Lake City, UT 84109, NDC 70285-1920-1

by Isomeric Pharmacy Solution, LLC

Reason: CGMP Deviations
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30 count HDPE bottles, Rx Only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0093-5721-56

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PROTONIX I.V. (pantoprazole sodium) for Injection, Equivalent to 40 mg pantoprazole per vial, For I.V. infusion only, Rx Only, Distributed by Wyeth Pharmaceuticals Inc, A subsidiary of Pfizer Inc, Philadelphia, PA 19101, Under license from Takeda GmbH, D78467 Konstanz, Germany, MADE IN FRANCE; packaged in A) Pfizer Injectables, 1 vial per carton (NDC 0008-0923-51) in a) bundles of 10 unit cartons (NDC 0008-0923-55) and b) 25 x 40 mg Vials per carton (NDC 0008-0923-60); B) NOVAPLUS, 1 vial per carton (NDC 00008-0941-01) in 25 x 40 mg Vials per carton (NDC 0008-0941-03); and C) PREMIERPro Rx, 1 vial per carton (NDC 0008-4001-01) in a) bundles of 10 unit cartons (NDC 0008-4001-10) and b) 25 x 40 mg Vials per carton (NDC 0008-4001-25).

by Pfizer Inc.

Reason: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month stability time point.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Gel Spice Co, Inc.

Product: 1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by…
Reason: Ground Turmeric may contain excess levels of lead.
Published: March 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Pioglitazone and Glimepiride Tablets, USP, 30 mg/4 mg, 30 count bottles, Rx only, Manufactured by Lek Pharmaceuticals d.d., Verovskova Ulica 57, Ljubljana, - SI-1526, Slovenia --- NDC 0781-5635-31

by Sandoz Inc

Reason: Failed Dissolution Specifications
Published: March 15, 2017
Distribution: Nationwide

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Data last updated: September 25, 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.