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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: PR ×
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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

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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

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

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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

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FDA Recall Terminated Historical recordClass II

Bupivacaine HCl Injection, single dose vial, Preservative Free 0.5%, 10mL (25/ct), Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-169-10

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

Azithromycin for Injection USP Vial, 500 mg per vial, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-174-10

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

Topex (benzocaine 20%), Topical Anesthetic Gel Strawberry, 1 oz, Rx only, Manufacturer: DS Healthcare, NDC 0699-5116-01

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

TobraDex (tobramycin and dexamethasone), Ophthalmic Ointment, 3.5 gm, Rx only, Manufacturer: Novartis, NDC 0078-0876-01

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

Miocol-E (acetylcholine chloride intraocular solution) 20 mg/2mL (10 mg/mL), Rx only, Manufacturer: Bausch & Lomb, NDC 24208-539-20

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 2-PAK (epinephrine injection, USP), Single-Dose Auto-Injectors 0.3 mg, Rx only, Manufactured for: Mylan Specialty LP., NDC 49502-500-02

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

Earache Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015. NDC 0363-3233-15

by Grato Holdings, Inc.

Reason: Microbial contamination of non-sterile product.
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Homeopathic EarAche Ear Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 59779-568-15

by Grato Holdings, Inc.

Reason: Microbial contamination of non-sterile product.
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Homeopathic EarAche Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: RITE AID, 30 Hunter Lane, Camp Hill, PA 17011. NDC 11822-3644-3

by Grato Holdings, Inc.

Reason: Microbial contamination of non-sterile product.
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dose Vial, 5 vials per Carton, Rx Only, Carton NDC 0703-1501-02, Distributed by: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, Vial NDC 0703-1501-01

by Teva Pharmaceuticals USA Inc

Reason: Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

B-Complex + Chromic Chloride (Choline Chloride 3%, Inositol 3%, Pyridoxine HCl 2%, Niacinamide 2%, Thiamine HCl 2%, Chlorobutanol 0.5%, Riboflavin 0.05%, Chromic Chloride 0.003%), 30 mL Multi-Dose Vial, packaged in 2 x 30 mL Multi-Dose Vials per carton, US Specialty Formulations, LLC, 116 Research Drive, Bethlehem, PA 18015, P/N: 234-15523

by US Specialty Formulations LLC

Reason: Lack of Assurance of Sterility
Published: June 15, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ethanol for Injection 95%, 67 mL Multi-Dose vial, Rx only, US Specialty Formulations, 1403 South Albert Street, Allentown, PA 18103, PN: 69389-06229

by US Specialty Formulations LLC

Reason: Lack of Assurance of Sterility
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.