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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 1, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass III

Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC 0025-2742-31), and b) 500-count bottles (NDC 0025-2742-51), Rx only, Distributed by G.D. Searle LLC, Division of Pfizer Inc, NY, NY 10017.

by Pfizer Inc.

Reason: Failed Dissolution Specification
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rocuronium Bromide 50 MG/5ML INJ., Qty: 5 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0222-57

by RemedyRePack Inc.

Reason: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Novolin 70/30, 100 Units/mL Solu., Qty: 1 Vial, MFG by: Novo Nordisk, A/S, Bagsvaerd, Denmark DK-2880, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0414-01

by RemedyRePack Inc.

Reason: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lorazepam 2 mg/mL Inj., Qty: 1 mL Vial, MFG by: West-Ward Pharma, Eatontown, NJ 07724, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0316-01

by RemedyRePack Inc.

Reason: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16

by RemedyRePack Inc.

Reason: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vitamin B-Complex 100, Multi MG Inj, Qty: 30 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0873-02

by RemedyRePack Inc.

Reason: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0253-03

by RemedyRePack Inc.

Reason: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Humulin 70/30, 100 Units/mL Inj, Qty: 10 mL Vial, MFG by: Lilly USA, LLC, Indianapolis, IN 46285, Repackaged by: Remedy Repack, Inc, 625 Kolter Dr, Indiana, PA 15701, NDC 52125-0415-08

by RemedyRePack Inc.

Reason: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

MECLIZINE HYDROCHLORIDE TABLETS, 25 mg, Packaged in a) 100 ct Bottles (NDC: 60429-205-01) and b) 1000 ct Bottles (NDC: 60429-205-10), Rx Only. Manufactured by: Par Pharmaceuticals Companies Inc., Spring Valley, NY 10977. Packaged by: GSMS Incorporated, Carmarillo, CA 93012.

by Golden State Medical Supply Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification for impurities.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

MECLIZINE HYDROCHLORIDE TABLETS, 12.5 mg, Packaged in 1000 ct Bottles, Rx Only. Manufactured by: Par Pharmaceuticals Companies Inc., Spring Valley, NY 10977. Packaged by: GSMS Incorporated, Carmarillo, CA 93012. NDC: 60429-204-10.

by Golden State Medical Supply Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification for impurities.
Published: December 16, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIC (HCG) Sublingual Drops, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIC (HCG) Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

METHYLFOLATE Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

METHYLFOLATE Capsules, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

TRI-EST Gels, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

TRI-EST Liquids, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

TRI-EST Lozenges, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

TRI-EST Capsules, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BI-EST Creams, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BI-EST Suspensions, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason: Penicillin Cross Contamination: potentially contaminated with penicillin
Published: December 9, 2015
Distribution: Nationwide

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Data last updated: October 1, 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.