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Recall totals

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

37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 recalls
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)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 14,741–14,760 of 20,823 recalls

FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 10 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-135-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed dissolution specifications - low dissolution results at S3 stage.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 5511-113-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed dissolution specifications - low dissolution results at S3 stage.
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 20 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-136-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed dissolution specifications - low dissolution results at S3 stage.
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Zenatane (isotretinoin) capsules, 40 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By: Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India,NDC 55111-137-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed dissolution specifications - low dissolution results at S3 stage.
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Nano PNC Water, packaged in amber glass bottles, Rx only, ICRPstudy.com, Immune Cellular Restoration Program.

by Pacific Medical Solutions

Reason
Marketed without an Approved NDA/ANDA and non-sterility: NANO PNC Water by nebulizer was sampled and found to contain variovorax paradoxus.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, NDC 45802-806-01, UPC 3 45802-806-01 7.

by L. Perrigo Company

Reason
Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC 45802-237-01, UPC 3 45802-237-01 9.

by L. Perrigo Company

Reason
Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Alfuzosin Hydrochloride Extended-release Tablets, 10 mg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, Gujarat, India, NDC 47335-956-88.

by Sun Pharmaceutical Industries, Inc.

Reason
Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg, Orange Flavor, 36 Chewable Tablets, a) packaged in 36-count bottle [UPC Code 369168288362 (FP0545)], b) bulk product (6K28817), OTC, Manufactured by: Allegiant Health Deer Park, NY 11729

by Allegiant Health

Reason
cGMP deviations - presence of rubber particles found loose in the bulk product.
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20

by United Exchange Corporation

Reason
Lack of assurance of sterility
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Eye Wash, 4 fl oz (118 mL) bottle, OTC, Distributed by: United Exchange Corp., 17211 Valley View Ave., Cerritos, CA 90703, Made in Korea, UPC Code: 780707005828

by United Exchange Corporation

Reason
Lack of assurance of sterility
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Eye Irrigating Solution, 4 fl oz (118 mL) bottle, OTC, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0536-1083-97

by United Exchange Corporation

Reason
Lack of assurance of sterility
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20

by United Exchange Corporation

Reason
Non-Sterility: Direct evidence of contamination for 2 lots based on FDA samples.
Published
March 8, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10

by Mylan Pharmaceuticals Inc.

Reason
Presence of Foreign Tablets/Capsules; bottles of Glipizide 5 mg tablets may contain Glipizide 10 mg tablets
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CycloSPORINE Capsules, USP, 100 mg, 30 count (5x6) blister cartons, Rx only, Distributed by American Health Packaging, Columbus, OH--- NDC 68084-921-25

by Amerisource Health Services

Reason
Failed Impurities/Degradations Specifications; out of specification results for Maximum Unknown Impurities and Total Impurities
Published
March 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Gamay Foods Inc

Product
Sharp Cheddar Cheese Seasoning, #125121, Net Weight 50 lbs.…
Reason
Gamay was notified by ingredient supplier that the milk powder ingredient was being recalled due to concerns about potential contamination with Salmonella.
Published
March 8, 2017
Distribution
WI and PA only.

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FDA Recall United States Terminated Historical recordClass II

Gamay Foods Inc

Product
Original Cheddar Cheese Seasoning, #117059, Net Weight 1600…
Reason
Gamay was notified by ingredient supplier that the milk powder ingredient was being recalled due to concerns about potential contamination with Salmonella.
Published
March 8, 2017
Distribution
WI and PA only.

View recall →

FDA Recall United States Terminated Historical recordClass I

Shearers Foods, Llc

Product
SPICY NACHO CHEESE TORTILLA CHIPS: Essential Everyday 10 oz…
Reason
The firm is recalling various snack products because they used ingredients received from Valley Milk Product which may be contaminated with Salmonella
Published
March 8, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Shearers Foods, Llc

Product
NACHO CHEESE TORTILLA CHIPS: Essential Everyday 1 oz bag (Mu…
Reason
The firm is recalling various snack products because they used ingredients received from Valley Milk Product which may be contaminated with Salmonella
Published
March 8, 2017
Distribution
Product was shipped to the following sta…

View recall →

FDA Recall United States Terminated Historical recordClass I

Shearers Foods, Llc

Product
Larry The Cable Guy Jalapeno' Popper Thin Potato Chips 3 oz…
Reason
The firm is recalling various snack products because they used ingredients received from Valley Milk Product which may be contaminated with Salmonella
Published
March 8, 2017
Distribution
Product was shipped to the following sta…

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.