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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: FL ×
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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

Oxycodone Hydrochloride Tablets, USP, 10 mg, 100 count bottle, Rx only, Marketed by: Rhodes Pharmaceuticals L.P., Coventry RI 02816, Manufactured by: Purdue Pharma L.P., Stanford, CT 06901 NDC 42858-002-01

by Rhodes Pharmaceuticals, L.P.

Reason: Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Naturo Aid Pharmaceutical Inc.

Product: Vita Aid SynerClear (Chocolate), VA-012. The product is a p…
Reason: Undeclared Milk. Products may be contaminated with milk residue.
Published: September 22, 2021
Distribution: Distributed in Arizona, California, Flor…

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FDA Recall United States Terminated Historical recordClass II

Naturo Aid Pharmaceutical Inc.

Product: Vita Aid SynerClear (Vanilla), VA-924. The product is a pow…
Reason: Undeclared Milk. Products may be contaminated with milk residue.
Published: September 22, 2021
Distribution: Distributed in Arizona, California, Flor…

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FDA Recall United States Terminated Historical recordClass II

Naturo Aid Pharmaceutical Inc.

Product: Vita Aid SynerClear (Unflavoured), VA-925. The product is a…
Reason: Undeclared Milk. Products may be contaminated with milk residue.
Published: September 22, 2021
Distribution: Distributed in Arizona, California, Flor…

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FDA Recall United States Terminated Historical recordClass II

Naturo Aid Pharmaceutical Inc.

Product: Vita Aid Keto-Elemental Nutrition (Thai), VA-958. The produ…
Reason: Undeclared Milk. Products may be contaminated with milk residue.
Published: September 22, 2021
Distribution: Distributed in Arizona, California, Flor…

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FDA Recall United States Terminated Historical recordClass II

Naturo Aid Pharmaceutical Inc.

Product: Vita Aid Keto-Elemental Nutrition (Chocolate), VA-958. The…
Reason: Undeclared Milk. Products may be contaminated with milk residue.
Published: September 22, 2021
Distribution: Distributed in Arizona, California, Flor…

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FDA Recall United States Terminated Historical recordClass I

Jimmy's Cookies, LLC

Product: Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 bla…
Reason: Undeclared allergen - Peanuts.
Published: September 22, 2021
Distribution: The recalled product was distributed to…

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FDA Recall Terminated Historical recordClass II

QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui Cosmetics Co., Ltd, Baiyun District, Guanzhou, China Distributed by Native Promotional Products, Tulsa, OK NDC 74447-010

by NATIVE PROMOTIONS, INC

Reason: Subpotent
Published: September 15, 2021
Distribution: Tribal nations in the following states:…

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FDA Recall United States Terminated Historical recordClass II

Ingredion

Product: Fermentation Derived Pepsin Product packaging: 5 individual…
Reason: Undeclared egg allergen
Published: September 15, 2021
Distribution: Distributed in the following states: CA,…

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FDA Recall Ongoing Historical recordClass II

aulief (Organic Camphor 3.00% Organic Menthol 5.00%), topical pain relief, packaged as a) 3.2 oz (90.7g) tube UPC 6 87806 30003 1 NDC 76305-302-01 ; b) 7.0 oz (198.5g) tube, UPC 6 87806 30007 9, NDC 76305-302-02; c) 16 oz (453.6g)Bottle w/ Pump, UPC 6 87806 30016 1, NDC 76305-302-03; Distributed by: CHINA-GEL LLC, Arlington Heights, IL 60005,

by China Gel Inc

Reason: CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

CHINA-GEL WHITE (Camphor 3.00%, Menthol 5.00%), A TOPICAL PAIN RELIEVER, packaged in a) 2 oz(56.8g) Tube, 76305-301-13 ; b) 4 oz (113.5 g) jar, UPC 6 87806 20004 1, NDC 76305-301-02 ; c) 6 OZ (170 g) tube, UPC 6 87806 20006 5, NDC 76305-301-03; d) 8 oz (226.8 g) Jar, UPC 6 87806 20008 9, NDC 76305-301-04; e) 16 oz ( 453.6 g) Bottle w/ Pump, UPC 6 87806 20016 4, NDC 76305-301-05; f) 120 oz (3.78L) gallon, UPC 6 87806 20128 4, NDC 76305-301-06: Distributed by: CHINA-GEL LLC, Arlington Heights, IL 60005,

by China Gel Inc

Reason: CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

CHINA_GEL (Camphor 3.00%, Menthol 5.00%) A TOPICAL PAIN RELIEVER, packaged as a) 2 OZ (56.8g) tube, NDC 76305-300-13; b) 4 OZ (113.5g) jar, UPC 6 87806 10004 2, NDC 76305-300-02; c) 6 OZ (170 g) tube, UPC 6 87806 10006 2, NDC 76305-300-03; d) 8 OZ (226.8g) jar, UPC 6 87806 10008 2, NDC 76305-300-04; e) 16 OZ (453.6g), Bottle w/ Pump, UPC 6 87806 10016 7, NDC 76305-300-03; f) 128 OZ (3.78L) Gallon, UPC 6 87806 10128 7, NDC 76305-300-06; Distributed by: CHINA-GEL LLC, Arlington Heights, IL 60005,

by China Gel Inc

Reason: CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clopidogrel Tablets, USP, 75 mg, 500-count bottle, Rx only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceutical Ltd., Baddi, Himachal, Pradesh, INDIA NDC 33342-060-15

by Macleods Pharma Usa Inc

Reason: Presence of foreign matter
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Artificial Tears Ointment, Lubricant Eye Ointment, Net Wt. 3.5 g (1/8 oz.) per tube, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-062-35

by Akorn, Inc.

Reason: Non-Sterility - OOS sterility testing observed during 12-month controlled room temperature stability testing. The microbiological investigation identified the organism as a member of the Bacillus cereus group.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lidocaine Ointment USP, 5% Rx Only, Net Wt 35.44 g(1 1/4 oz)packaged in a laminat tube, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-008-14.

by Teligent Pharma, Inc.

Reason: Failed Viscosity Specifications: lot does not meet specification for Viscosity, which was determined through routine testing.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. India, Marketed by: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801 NDC 59746-329-90

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Subpotent
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8 Fl OZ (236 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200. Distributed by SBL Brands, LLC Las Vegas, NV 89119 UPC: 6 76753 00420 8 ,

by Global Sanitizers LLC

Reason: CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1 ,

by Global Sanitizers LLC

Reason: CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1

by Global Sanitizers LLC

Reason: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and to contain methanol.
Published: September 8, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8 FL OZ (236 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200, Distributed by SBL Brands, LLC. Las Vegas, NV 89119. Made in Mexico UPC: 6 76753 00420 8,

by Global Sanitizers LLC

Reason: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and to contain methanol.
Published: September 8, 2021
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.