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

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Source: FDA and USDA public dataLast updated September 12, 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

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

Alprazolam Tab, USP 0.5mg, (CIV), packaged in: a) 30-count bottle (NDC 68788-7595-3), b) 60-count bottle (NDC 68788-7595-6), c) 90-count bottle (NDC 68788-7595-9); Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL.

by Preferred Pharmaceuticals, Inc.

Reason: CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tab, USP 0.25mg, (CIV), 30-count bottle, Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL. Ins:NDC 68788-7594-3

by Preferred Pharmaceuticals, Inc.

Reason: CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Simvastatin 40 mg tablets, packaged in a) 30-count bottles (NDC 70518-0060-01) and b) 90-count bottles (NDC 70518-0060-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rosuvastatin 40mg tablets, packaged in a) 45-count bottles (NDC 70518-1311-01), and b) 90-count bottles (NDC 70518-0484-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rosuvastatin 10mg tablets, packaged in a) 30-count bottles (NDC 70518-0375-03 and 70518-0375-01) and b) 90-count bottles (NDC 70518-0375-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rosuvastatin 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-3519-00

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ropinirole 2mg tablets, packaged in 180-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC70518-2750-00

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Atorvastatin 20 mg tablets, packaged in a) 30-count bottles (NDC 70518-1977-00) and b)90-count bottles (NDC 70518-1977-01), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tadalafil 5 mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2972-00

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Simvastatin 10 mg tablets, packaged in a) 30-count bottles (NDC 70518-0064-01) and b) 90-count bottles (NDC 70518-0064-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rosuvastatin 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-3519-00.

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ropinirole 0.5 mg tablets, packaged in 90-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2439-00.

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Glimepiride 2 mg tablets, packaged in a) 30-count bottles (NDC 70518-0405-03), b) 90-count bottles (NDC 70518-0405-00) and c)180-count bottles (NDC 70518-0405-02), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Doxazosin 2 mg tablets, packaged in a) 30-count (NDC 70518-1560-00) and b) 90-count bottles (NDC 70518-1560-01), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Atorvastatin 10 mg tablets, packaged in a) 30-count bottles (NDC 70518-1946-00) and b) 90-count bottles (NDC 70518-1946-01), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Aripiprazole 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2921-03

by RemedyRePack Inc.

Reason: cGMP Deviations
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection, USP, CIII, 200 mg/mL, packaged in: a) 10 mL multiple-dose vials (NDC 52536-625-10) and b) 1 mL single dose vials (NDC 52536-625-01), Rx only, Mfd for: Wilshire Pharmaceuticals, Inc., Atlanta, GA 30328.

by Azurity Pharmaceuticals, Inc.

Reason: cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Perrigo Nutritionals

Product: Gerber GoodStart SoothePro Infant Formula with Iron. Milk…
Reason: Infant Formula has the potential to be contaminated with Cronobacter spp.
Published: April 12, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Dabigatran Etexilate 150mg Capsules, 150 mg, Rx Only, 60 Capsules per bottle, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054, NDC 67877-475-60.

by Ascend Laboratories, LLC

Reason: CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Dabigatran Etexilate Capsules, 75 mg, Rx Only, 60 Capsules per bottle, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-474-60.

by Ascend Laboratories, LLC

Reason: CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.
Published: April 5, 2023
Distribution: Nationwide

View recall →

Data last updated: September 12, 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.