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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: UT ×
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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

CEFAZOLIN 5mg/mL/HEPARIN 100unit/ml 1.5ML SYR, antibiotic, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

CEFAZOLIN (a) 12GM IN NS 600ML, (b) 2GM IN NS 100ML, (c) 2GM/20ML SW SYRINGE, (d) 3GM IN NS 150ML, antibiotic, used with a curlin, home or no pump assigned. Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

CASPOFUNGIN 50MG IN NS 100ML, used with a HOMEPUMP, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin/Sulbactam 3GM IN NS 100ML, antibiotic, Rx only, used with a home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AMPICILLIN 8GM IN NS 400ML, antibiotic, used with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AMPICILLIN 12GM IN NS 600M, used with a Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amikacin 450MG IN NS 45ML, Antibiotic, used in a HOMEPUMP, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300 Chesapeake, VA 23320,

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride, used as a diluent or hydration, packaged volume of (a)1000ML (b)2000ML (c) 720ML, used with Curlin pump, no pump or gravity. Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320

by Sentara Infusion Services

Reason: Lack of sterility assurance
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure, distributed by: DERMAL SOURCE, Portland, OR, www.dermalsource.com, 1-866-568-3223, NDC code: 80069-012-01, Drug Facts- For use by licensed professionals only' Active Ingredients- Lidocaine HCL (5%), Epinephrine (0.01%).

by HTO Nevada, Inc.

Reason: cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

New & Improved Blue Gel Anesthetic, to reduce pain and swelling during pain sensitive procedures, 1 oz bottle, distributed by Dermal Source, Portland, OR, www.dermalsource.com 1-888-568-3223. NDC Code: 80069-008-01. Drug Facts- For use by licensed professionals only, Active Ingredients -Lidocaine HCL (5%), Tetracaine HCL (1%) and epinephrine (0.1%).

by HTO Nevada, Inc.

Reason: cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, packaged in (a) 100-count bottle, NDC 68001-501-00; (b) 500-count bottle, NDC 68001-501-03. Manufactured by Alkem Laboratories Ltd., India. For BluePoint Laboratories

by Amerisource Health Services LLC

Reason: Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL), Riboflavin 30 mg/30 mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW INTRAVENOUS USE, 30 mL Sterile Multiple Use Vial, Rx Only, Compounded for a licensed professional or patient use by: McGuff Compounding Pharmacy Services, Inc, Santa Ana, CA 92704.

by McGuff Compounding Pharmacy Services, Inc.

Reason: Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thiamine Hydrochloride 200 mg/2mL (100mg/mL), Riboflavin 2 mg/2mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW INTRAVENOUS USE, 2 mL Sterile Single Use Vial, Preservative-Free, Rx Only, Compounded for a licensed professional or patient use by: McGuff Compounding Pharmacy Services, Inc, Santa Ana, CA 92704.

by McGuff Compounding Pharmacy Services, Inc.

Reason: Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pepsico Inc

Product: Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 F…
Reason: Foreign object (glass).
Published: February 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Posaconazole Delayed-Release Tablets, 100 mg, 60-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009; Manufactured by: Biocon Pharma Limited, Bengaluru, India - 560 099, NDC 70377-038-11.

by BIOCON PHARMA INC

Reason: Failed Impurities/Degradation Specifications: High Out Of Specification degradation results.
Published: February 15, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL bottle, Sterile, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. NDC: 17478-215-02

by Akorn, Inc.

Reason: Failed Stability Specifications: Out of specification test results for viscosity was identified at the 12M stability timepoint.
Published: February 15, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, 8 FL OZ (237 ML) bottles.

by Urban Electric Power

Reason: CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Published: February 15, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v), packaged in a) 2 FL OZ (60 ML), b) 3 FL OZ (88 ML) bottles, c) 10 FL OZ (295 ML) bottles, d)12 FL OZ (355 ML) bottles, e)16 FL OZ (473 ML) bottles, f) 64 FL OZ (1892 ML) bottles, g) 128 FL OZ (3785 ML) bottles

by Urban Electric Power

Reason: CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Published: February 15, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Mondelez Global Llc

Product: Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UP…
Reason: Undeclared FD&C Yellow No. 5
Published: February 15, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ortho Molecular Products, Inc.

Product: Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, p…
Reason: Raw material tested positive for Cronobacter sakazakii.
Published: February 15, 2023
Distribution: Nationwide

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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.