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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

Albuterol Sulfate Inhalation Solution, 0.021%, 0.63 mg/3mL, packaged in 30 x 3 mL Sterile Unit-Dose Vials, Rx only, MFG: Nephron Pharma, NDC 0487-0301-01

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

GlucaGen (glucagon) for injection, 1 mg per vial, single dose kit, Rx only, Manufactured for: Boehringer Mannheim, NDC 0597-0260-10

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

Firmagon (degarelix for injection) 240 mg, Starting Dose, packaged in a kit, Rx only, MFG: Ferring Pharmaceuticals Inc., NDC 55566-8403-01

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

Firmagon (degarelix for injection) 80 mg, Maintenance Dose (28 days), packaged in a kit, Rx only, MFG: Ferring Pharmaceuticals Inc., NDC 55566-8303-01

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

Epinephrine Injection, USP, Single-Dose Auto-Injectors 0.15 mg, packaged in 2 count carton, Rx only, MFG: Mylan Pharma NDC 49502-101-02

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

Epinephrine Injection, USP, Single-Dose Auto-Injectors 0.3 mg, packaged in 2 count carton, Rx only, MFG: Mylan Pharma, NDC 49502-102-02

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

EPI-Pen Jr, 2-PAK, (epinephrine injection, USP) Single-Dose Auto-Injectors 0.15 mg, packaged in 2 count carton, Rx only, MFG: Mylan Pharma, NDC 49502-501-02

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

Dihydroergotamine Mesylate, Injection, USP, 1mg/mL, packaged in box of 5 x 1 mL ampules, Rx only, Manufactured for: Perrigo, Minneapolis, MN, NDC 0574-0850-10

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

Epidural Tray, Nerve Block Single shot, Rx only, # 182207, MFG: Avanos Medical Sales LLC

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

Ampicillin for Injection, USP, 1 g per vial, 10-count box, Rx only, Distributed by: Auromedics Pharma, NDC 55150-113-10

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

Betadine 5%, Sterile Ophthalmic Prep Solution, (povidine-iodine ophthalmic solution), 1 fl. oz. (30 mL), Rx only, Mfd for: Alcon Surgical Inc., NDC 0065-0411-30

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

Sumatriptan Injection, USP, 6mg/0.5 mL, packaged in a box of 5 x 0.5 mL single-dose vials, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0173-01

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

Arzol (Silver Nitrate Applicator), (Silver Nitrate 75%, Potassium Nitrate 25%), 100-count box, Rx only, Manufacturer: Arzol Chemical Co, NDC 12870-0001-02

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

Olanzapine single dose vial Lyophilized, 10 mg, Rx only, MFG: Auromedics Pharma LLC, NDC# 55150-0308-01

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

Lidocaine Patch, 5%, 30-count box, Rx only, Manufacturer: Rhodes Pharmaceuticals, NDC 42858-0118-30

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

Dexmedetomidine HCL Single Dose Vial 200 mcg per 2 mL (100mcg/mL), Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0209-02

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

Bupivacaine HCl Injection, Single Dose Vial, 0.75%, 10 mL/7.5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0171-10

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

Bupivacaine HCl Injection, Multi dose vial, 0.50%, 50 mL/5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0250-50

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

Bupivacaine HCl Injection, Multi dose vial, 0.25%, 50 mL/2.5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0249-50

by Mckesson Medical-Surgical Inc. Corporate Office

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

View recall →

FDA Recall Terminated Historical recordClass II

Bupivacaine HCl Injection, single dose vial, 0.5%, 30 mL/5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0170-30

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.