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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,113
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,781–5,800 of 18,718 recalls

FDA Recall United States Terminated Historical recordClass I

Fresh Express Inc (Div of Chiquita Brands)

Product
"Baby Kale" (salad product) packed in 5oz. packages
Reason
potential to be contaminated with Listeria monocytogenes
Published
February 2, 2022
Distribution
Products were distributed to 110 domesti…

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FDA Recall United States Terminated Historical recordClass I

Fresh Express Inc (Div of Chiquita Brands)

Product
"Baby Greens" (salad product) packed in 6oz. packages
Reason
potential to be contaminated with Listeria monocytogenes
Published
February 2, 2022
Distribution
Products were distributed to 110 domesti…

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FDA Recall United States Terminated Historical recordClass I

Fresh Express Inc (Div of Chiquita Brands)

Product
"Avocado Ranch" (salad product) packed in 9.7oz. and 12.8oz.…
Reason
potential to be contaminated with Listeria monocytogenes
Published
February 2, 2022
Distribution
Products were distributed to 110 domesti…

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FDA Recall United States Terminated Historical recordClass I

Fresh Express Inc (Div of Chiquita Brands)

Product
"Asian Avocado" (salad product) packed in 9.7oz. packages
Reason
potential to be contaminated with Listeria monocytogenes
Published
February 2, 2022
Distribution
Products were distributed to 110 domesti…

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FDA Recall United States Terminated Historical recordClass I

Fresh Express Inc (Div of Chiquita Brands)

Product
"Angel Hair" (salad product) packed in 10oz. packages
Reason
potential to be contaminated with Listeria monocytogenes
Published
February 2, 2022
Distribution
Products were distributed to 110 domesti…

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FDA Recall United States Terminated Historical recordClass I

Fresh Express Inc (Div of Chiquita Brands)

Product
"American" (salad product) packed in 11oz. and 24oz. package…
Reason
potential to be contaminated with Listeria monocytogenes
Published
February 2, 2022
Distribution
Products were distributed to 110 domesti…

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FDA Recall United States Terminated Historical recordClass I

Fresh Express Inc (Div of Chiquita Brands)

Product
"5- Lettuce Mix" (salad product) packed in 6oz. packages
Reason
potential to be contaminated with Listeria monocytogenes
Published
February 2, 2022
Distribution
Products were distributed to 110 domesti…

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FDA Recall Terminated Historical recordClass II

Medique Pain-Off (Acetaminophen 250 mg, Aspirin (NSAID*) 250 mg, Caffeine 65 mg) Tablets, packaged in 2-count Tablets per Unit Dose Packet, packaged as a) 200-count Tablets (100 x 2) Unit Dose packets per carton, UPC 3 47682 22847 7, Reorder #22847; b) 500-count Tablets (250 x 2) Unit Dose packets per carton, UPC 3 47682 22813 2, Reorder #22813; c) 100-count Tablets (50 x 2) Unit Dose packets per carton, UPC 3 47682 22833 0, Reorder #22833; d) 24-count Tablets (12 x 2) Unit Dose packets per carton, UPC 3 47682 22864 4, Reorder #22864; Manufactured for Medique Products, Fort Myers, FL 33967.

by Medique Products

Reason
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-058-04

by VistaPharm, Inc.

Reason
Failed Stability Specifications
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3 mL Prefilled Pens per carton (NDC 49502-0196-75), Rx only, Manufactured in Malaysia for: Mylan Specialty L.P., Morgantown, WV, 26505.

by MYLAN PHARMACEUTICALS INC

Reason
Labeling: Missing Label: label missing from some Semglee prefilled pens.
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Extra Strength Headache (acetaminophen 250 mg, aspirin 250 mg, caffeine 65 mg) tablets, packaged in 2-count tablets per packet, Manufactured for: Lil' Drug Store Products, Inc., Cedar Rapids, IA 52404

by Medique Products

Reason
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin (NSAID), and Caffeine], 250 mg, 250 mg, 65 mg, packaged as 100-count Tablets (50 Packets, 2 tablets each) per carton, Manufactured for: Acme United Corporation 55 Walls Dr, Fairfield, CT 06824, UPC 0 73577 90316 6

by Medique Products

Reason
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3

by Dr. Reddy's Laboratories, Inc.

Reason
Subpotent drug
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville, NC 27834, NDC 51862-604-50

by Mayne Pharma Inc

Reason
CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Leader, 12HR Allergy & Congestion Relief, Fexofenadine HCl, 60mg Pseudoephedrine HCl 120mg Antihistamine Nasal Decongestant, 20 Extended Release Tablets per box, NDC 70000-0518-1, Distributed by Cardinal Health, Dublin, Ohio 43077, Made in India.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

CVS Health, Allergy Relief D, Fexofenadine HCl 60mg/Antihistamine Pseudoephedrine HCl 120mg/Nasal Decongestant, a) 20 Extended Release Tablets per box, UPC 050428436189, b) 30 Extended Release Tablets per box, UPC 050428290538, Distributed by CVS Pharmacy Inc., One CVS Drive, Woonsocket, RI, 02895, Made in India.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

QC QUALITY CHOICE, Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release Tablets, USP, Allergy & Congestion, 10 Tablets per box, NDC 63868-729-10, Distributed by C.D.M.A., Inc., 43157 W 9 Mile Rd, Novi, MI 48375, Made in India.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

equate, Allergy Relief D, Fexofenadine HCl 60mg/Antihistamine, Pseudoephedrine HCl 120mg/Nasal Decongestant Extended-Release Tablets USP, a) 20 Extended Release Tablets per box, NDC 49035-273-20, b) 30 Extended Release Tablets per box, NDC 49035-273-30, Distributed by: Walmart Inc., Bentonville, AR 72716, Product of India.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Dr. Reddys, Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets USP, a) 10 tablets per box, UPC 343598823355, b) 20 tablets per box, UPC 343598823140, c) 30 tablets per box, UPC 343598823317, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Made in India.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications
Published
January 26, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Kroger, Allergy Relief-D, Fexofenadine HCl 60mg/Antihistamine Pseudoephedrine HCl 120mg/Nasal Decongestant, Extended-Release Tablets USP, 20 tablets per box, NDC 30142-611-14, Distributed by the Kroger Co., Cincinnati, Ohio, 45202, Made in India.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications
Published
January 26, 2022
Distribution
Nationwide

View recall →

Data last updated:

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.