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Recall totals

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

37,116

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potatoPublished September 16, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 18, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 60 mg Antihistamine, 12HR, packaged as a) 12 count bottle, NDC 59779-425-53, UPC 0 50428 25414 1; b)24 count bottle, NDC 59779-425-62, UPC 0 50428 53435 9; Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, Made in Czech Republic

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

CAREONE Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, packaged as a)30 count bottle, NDC 41520-229-39, UPC 3 41520 31984 6; b)45 count bottle, NDC 41520-229-95 UPC 3 41520 31983 9; Made in the Czech Republic, Distributed by: Foodhold U.S.A. LLC Landover, MD 20785. Made in Czech Republic

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

berkley jensen, ALLERGY RELIEF, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, 150 count bottle, Made in the Czech Republic, Distributed by: BJ's WHolesale Club 25 Research Drive Westborough, MA 01581

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

basic+care, allergy Fexofenadine Hydrochloride Tablets, 60 mg/Antihistamine, 12HR, 100 count bottle, Made in the Czech Republic, Distributed by: Perrigo Allergan, MI 49010, NDC 0113-7425-78 UPC 3 70030 14536 2

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

basic+care, allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 150 count bottle, Made in the Czech Republic, Distributed by: Perrigo Allergan, MI 49010, NDC 0113-7571-47 UPC 3 70030 11470 2

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

amazon, Allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 30 count bottle, Made in the Czech Republic, Distributed by: Amazon.com Services LLC 410 Terry Avenue N. Seattle, WA 98109 UPC 3 70030 11466 5

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GoodSense Aller.Ease, Fexofenadine hydrochloride 12 HR, 60 mg tablets, 24 count bottle, UPC 3 0113 0425 62 7; Made in the Czech Republic, Distributed by: Perrigo Allergan MI 49010.

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22, UPC 0 41163 48067 4; b) 70 tablets per bottle, NDC 41163-571-01, UPC 0 41163 49847 1; Made in the Czech Republic, Distributed by: UNFI Providence, RI 02908.

by Perrigo Company PLC

Reason: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Gatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-435-01.

by Lupin Pharmaceuticals Inc.

Reason: Failed Stability Specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration.
Published: January 12, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles, Distributed by: Valisa MFG, LLC, Farmingdale, NY, 11735, Made in USA, UPC 6 86162 99246 1

by Valisa MFG LLC

Reason: Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sodium Bicarbonate in 5% Dextrose Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-326-03

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine HCl, 50 mg per 250 mL, (200 mg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-901-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine HCl, 40 mg per 250 mL, (160 mcg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-252-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NOREPINEPHRINE, 16 mg per 250 mL, (64 mcg per mL) in 0.9% Sodium Chloride Injection, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-926-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NOREPINEPHRINE, 8 mg per 250 mL, (32 mcg per mL) in 0.9% Sodium Chloride Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-676-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NOREPINEPHRINE, 4 mg per 250 mL, (18 mcg per mL) in 0.9% Sodium Chloride Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-651-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NOREPINEPHRINE, 16 mg per 250 mL, (64 mcg per mL) in 5% Dextrose Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-002-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MORPHINE SULFATE, in 0.9% Sodium Chloride Injection, 50 mg per 50 mL, (1 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-427-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Fentanyl Citrate, in 0.9% Sodium Chloride Injection, 2.5 mg per 250 mL, (10 mcg per mL), Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-327-02.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Fentanyl Citrate, in 0.9% Sodium Chloride Injection, 1 mg per 100 mL, (10 mcg per mL), Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-327-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: January 5, 2022
Distribution: Nationwide

View recall →

Data last updated: September 18, 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.