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

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Source: FDA and USDA public dataLast updated September 13, 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

Propofol Injectable Emulsion, USP 200 mg per 20 mL (10 mg per mL), twenty-five 20 mL vials, Rx only, MFG: Teva Pharma USA, NDC 0591-2136-95

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Propofol Injectable Emulsion, USP, 200 mg/ 20 mL (10 mg/mL), packaged in a) 50 mL vial, in packs of 20 (NDC 00591-2136-51), b) 100 mL vial, in packs of 10 (NDC 00591-2136-68), Rx only, MFG: Teva Pharma USA

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Proair, HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 metered inhalations, Rx only, MFG: Teva Pharma USA, NDC 59310-579-22

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Mupirocin Ointment, USP 2%, 22 grams tube, Rx only, MFG: Teva Pharma USA, NDC 0093-1010-42, MFG: Teva Pharma USA

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension USP, 400 mg/5mL (80 mg/mL), 5 mL multi-dose vials, Rx only, MFG: Teva Pharma USA, NDC 0703-0063-01

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, packaged in a) 1 mL single dose vial (NDC 0703-0051-01) b) 25-count box (NDC 0703-0051-04), Rx only, MFG: Teva Pharma USA

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension USP, 400 mg/10 mL (40 mg/mL), 10 mL multi-dose vial, Rx only, MFG: Teva Pharma USA, NDC 0703-0045-01

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension, USP, 200mg/5mL (40 mg/mL), 5 mL multi-dose vial, Rx only, MFG: Teva Pharma USA, NDC 0703-0043-01

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension, USP, 40 mg/mL, packaged in a) 1 mL single dose vial (NDC 0703-0031-01), b) 25-count box (NDC 0703-0031-04), Rx only, MFG: Teva Pharma USA

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Medroxyprogesterone acetate injectable suspension, USP, 150 mg/mL, 1 mL vials, packaged in a) single dose vial (NDC 0703-6801-01), b) 25-count box single dose vials (NDC 0703-6801-04), Rx only, MFG: Teva Pharma USA

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lidocaine Patch 5%, 30-count box, Rx only, MFG: Teva Pharma USA, NDC 0591-3525-30

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levalbuterol Tartrate HFA Inhalation Aerosol, 45 mcg/actuation, 200 metered inhalations, Rx only, MFG: Teva Pharma USA, NDC 0591-2927-54

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottle, Rx only, MFG: Teva/Actavis, NDC 00228-2127-10

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ketoconazole Cream, 2%, Net Wt 60 grams tube, Rx only, MFG: Nycomed Inc, NDC 0168-0099-60

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension USP, 400 mg/5 mL (80 mg/mL), 5 mL Multiple Dose Vial, Rx only, MFG: NorthstarRx/Teva Pharma USA, NDC 16714-473-01

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension, USP, 400 mg/10 mL (40 mg/mL), 10 mL Multiple Dose Vial, Rx only, MFG: NorthstarRx/Teva Pharma USA, NDC 16714-090-01

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension, USP, 200 mg/5 mL (40 mg/mL), 5 mL Multiple Dose Vial, Rx only, MFG: NorthstarRx/Teva Pharma USA , NDC 16714-089-01

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MethyLPREDNISolone Acetate Injectable Suspension USP, 40 mg/mL, packaged in a) single dose vial (NDC 6714-088-01) b) 25-count box (NDC16714-088-25), Rx only, MFG: NorthstarRx/Teva Pharma USA

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Medroxyprogesterone acetate injectable suspension, 150 mg/mL, 1 mL single dose vial, Rx only, MFG: NorthStarRx/Teva Pharma USA , NDC 16714-981-01

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg, 100-count unit dose box, Rx only, MFG: Major Pharma, NDC 0904-2725-61

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: cGMP deviations: Temperature abuse
Published: June 15, 2022
Distribution: Nationwide

View recall →

Data last updated: September 13, 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.