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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 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

Doxycycline Capsules, USP, 100 mg, 50-count bottle, Rx only, Distributed by: Sun Pharmaceuticals, NDC 63304-616-50

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

Sterile Water for Injection USP, 2000 mL, Rx only, Baxter Healthcare Corp., NDC 0338-0013-06

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

Spinal Tray (A4058-25 Spinal Tray 25G Whitacre No Epinephrine), Rx only, Manufacturer: Smiths Medical ASD, Inc., NJ

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

Ciprofloxacin Ophthalmic Solution 0.3%, 10 mL bottle, Rx only, Manufactured by: Alcon Laboratories, Inc., NDC 61314-0656-10

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

Betamethasone Dipropionate Cream USP, 0.05%, 45 grams tube, Rx only, MFG: Sandoz Pharma, NDC 0168-0055-46

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

Aprepitant Capsule, USP, 40 mg, 1 capsule per unit dose package, Rx only, MFG: Sandoz Pharma, NDC 0781-2321-06

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

Aparaclonidine Ophthalmic Solution 0.5% as base, 0.5%, 5 mL bottle, Rx only, MFG:Sandoz Pharma, NDC 61314-665-05

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

Amoxicillin Capsules, USP, 500 mg, 100-count bottle, Rx only, MFG: Sandoz Pharma, NDC 0781-2613-01

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

Albuterol Sulfate Inhalation Aerosol HFA 90 mcg, with Dose Indicator, 200 metered inhalations, Rx only, Distributed by: Sandoz Inc., NDC 0781-7296-85

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

Albuterol Sulfate Inhalation Aerosol HFA with Dose Indicator, 90 mcg, 200 metered inhalations, Rx only, Manufactured for: PAR Pharmaceutical, NDC 0254-1007-52

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

Adrenalin (epinephrine injection, USP) 30 mg/30 mL (1mg/mL), 30 mL multiple dose vial, Rx only, MFG: Par Pharma, NDC 42023-168-01

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 III

Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution 3mL vial, packaged in a) 30-count (NDC 0487-0201-03), b) 60-count (NDC 0487-0201-60), Rx only, MFG: Nephron Pharma

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

Albuterol Sulfate Inhalation Solution 0.083%, 2.5 mg/3mL, packaged in 25 X 3mL unit-dose vials, Rx only, MFG by: Nephron Pharma, NDC 0487-9501-25

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

Albuterol Sulfate Inhalation Solution 0.083%, 2.5 mg/3mL, packaged in 5 x 3 mL unit-dose vials, Rx only, Manufactured by: Nephron Pharma, NDC 0487-9501-03

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

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

View recall →

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

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.