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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 October 2026.

37,271
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 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

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)

  • 1,739 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

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

Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 2,541–2,560 of 17,412 recalls

FDA Recall OngoingHistorical recordClass II

DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose, packaged in 6000mL bags, Rx only, Fresenius Medical Care NA Waltham, MA 02451, NDC 49230-206-62.

by Fresenius Medical Care Holdings, Inc.

Reason
Lack of Sterility Assurance
Published
January 10, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: April 24, 2024Historical recordClass III

Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: Azurity Pharmaceuticals, Woburn, MA 01801, NDC 52652-9001-1

by Azurity Pharmaceuticals, Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
Published
January 10, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 18, 2024Historical recordClass II

BioMylz Pvt. Ltd.

Product
Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor…
Reason
Potential mold contamination
Published
January 10, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06

by TCP HRB ACQUISITON LLC

Reason
Chemical contamination: Presence of benzene
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06

by TCP HRB ACQUISITON LLC

Reason
Chemical contamination: Presence of benzene
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA

by TCP HRB ACQUISITON LLC

Reason
Chemical contamination: Presence of benzene
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759 99300 7. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ

by Meta Herbal

Reason
Marketed without an approved NDA/ANDA: Magnum XXL found to contain undeclared active pharmaceutical ingredient (API) - Sildenafil.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2025Historical recordClass II

Thiamine HCl/Pyridoxine HCl 20 mg/mL /100mg/ml Injection Solution, 30mL Amber Glass Vial, Rx only, AnazaoHealth, 7465 W. Sunset Road, Las Vegas, NV, NDC 72682-8721-3.

by AnazaoHealth Corporation

Reason
Presence of Particulate Matter.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2025Historical recordClass II

B-Complex, Thiamine HCI / Riboflavin / Niacinamide / Dexpanthenol / Pyridoxine HCI injection, 74/2/75/2/2 MG/ML, 30ML Sterile Multiple-Dose Vial, Rx only, AnazaoHealth, 7465 W Sunset Rd #1200, Las Vegas, NV 89113, NDC 72682-2230-3

by AnazaoHealth Corporation

Reason
Presence of Particulate Matter.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Inhub Wixela (fluticasone propionate and salmeterol inhalation powder, USP) 500/50MCG, 60 Doses of Inhalation Powder, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-9320-32

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Warfarin Sodium Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1721-01

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Warfarin Sodium Tablets, USP, 2.5 mg, 100 Tablets per bottle, Rx only, Manufactured For: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1714-01

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Triamterene and Hydrochlorothiazide Capsules, USP, 37.5 mg/25 mg, 100 capsules per bottle, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19136. NDC 0527-1632-01

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Terconazole Vaginal Suppositories, 80 mg, 3 Suppositories with Vaginal Applicator, Rx only, Manufactured by: Cosette Pharmaceuticals, Inc., 111 Coolidge Street, South Plainfield, NJ 07080. NDC: 0713-0552-73

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

SPIRIVA HANDIHALER (tiotropium bromide inhalation powder) 18 mcg/Capsule, 30 capsules, 3 blister cards, each card contains 10 capsules, Rx only, For oral inhalation only, Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA. NDC: 0597-0075-41

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

RIVASTIGMINE TRANSDERMAL SYSTEM, Delivers 4.6 mg/24 hours, 30 systems per box, Rx Only, Distributed by: Alvogen, Inc., Morristown, NJ 07960. NDC 47781-304-03

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Ricola CherryHoney Herb Throat Drops (menthol, 1.8 mg), 10 Drops per roll, Manufacturer: Ricola Ltd., 4242 Laufen, Switzerland; Distributed by: Ricola USA Inc., 6 Campus Drive, 2nd Floor South, Parsippany, NJ 07054. NDC: 54305-507-10

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Propranolol Hydrochloride Tablets, 20 mg, 100 Tablets per bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC: 69238-2078-1

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

PredniSONE Tablets, USP, 20 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801. NDC: 59746-175-06

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2024Historical recordClass II

Nyamyc, 100,000 USP units per gram, 60 grams, Rx only, Topical Use Only, Manufactured by: Upsher-Smith Laboratories, Inc, Minneapolis, MN 55447.

by CARDINAL HEALTHCARE

Reason
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published
January 3, 2024
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.

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