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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to October 2026.

37,324

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

State: WA ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 21, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

FDA Recall TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: February 20, 2026Historical 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 TerminatedTerminated: November 17, 2023Historical 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 TerminatedTerminated: November 17, 2023Historical 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 TerminatedTerminated: May 12, 2024Historical 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 TerminatedTerminated: April 27, 2023Historical 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 TerminatedTerminated: April 27, 2023Historical 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 TerminatedTerminated: May 22, 2023Historical recordClass II

Amlag & Quibuyen, LLC dba Hood Famous Bake Shop

Product: Coconut Pandan Cheesecake Coconut Butter Biscuit Crust (4oz…
Reason: Coconut Pandan cheesecake is recalled because Sulfite is not declared as a coconut milk s sub-ingredient and Coconut is not declared in the Contains statement.
Published: February 22, 2023
Distribution: Distributed in WA.

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FDA Recall United States TerminatedTerminated: May 22, 2023Historical recordClass II

Amlag & Quibuyen, LLC dba Hood Famous Bake Shop

Product: Vietnamese Coffee Cheesecake Coconut Butter Biscuit Crust (4…
Reason: Vietnamese Coffee cheesecake is recalled because Coconut is declared in the ingredients statement, but Coconut is not declared in the Contains statement.
Published: February 22, 2023
Distribution: Distributed in WA.

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FDA Recall United States TerminatedTerminated: May 22, 2023Historical recordClass II

Amlag & Quibuyen, LLC dba Hood Famous Bake Shop

Product: White Chocolate Guava Cheesecake Coconut Butter Biscuit Crus…
Reason: White Chocolate Guava cheesecake is recalled because Soy lecithin and Coconut are not declared in the Contains statement.
Published: February 22, 2023
Distribution: Distributed in WA.

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FDA Recall United States TerminatedTerminated: May 22, 2023Historical recordClass II

Amlag & Quibuyen, LLC dba Hood Famous Bake Shop

Product: Ube (Purple Yam) Cheesecake Coconut Butter Biscuit Crust (4o…
Reason: Ube cheesecake is recalled because Coconut is declared in the ingredients statement, but Coconut is not declared in the Contains statement.
Published: February 22, 2023
Distribution: Distributed in WA.

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FDA Recall United States TerminatedTerminated: July 20, 2023Historical 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 TerminatedTerminated: June 21, 2024Historical 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 OngoingHistorical 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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Data last updated: October 21, 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.