Data Explorer

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.

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

State: HI ×
Clear all

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.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated September 28, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

Download CSV

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass II

Nu Skin Enterprises Inc.

Product: Pharmanex BioGinkgo. Mental Sharpness. 60 Tablets
Reason: Nu Skin announces a voluntary field action for Pharmanex BioGinkgo due to undeclared allergen; wheat.
Published: March 15, 2017
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

McCormick & Co Inc. Spice Mill Plant

Product: McCormick & Co., Inc., Stubbs Barbecue. 18oz Best By Date…
Reason: McCormick & Co., Inc., has decided to initiated a voluntary recall of there Stubbs Sticky Sweet BBQ Sauce 18oz Bottle. Best By Date of January 17, 2020. Because of a glass bottle defect. The glass defect involves various thickness and defects that may result in chipped or missing glass.
Published: March 15, 2017
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Robert Rothschild Farm LLC

Product: Gift Sets with Chocolate Pretzel Dippers
Reason: The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.
Published: March 15, 2017
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Robert Rothschild Farm LLC

Product: Gift Sets with Pretzel Twists
Reason: The product is not labeled with an ingredient statement and therefore, does not declare the allergens, soy and wheat.
Published: March 15, 2017
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

NSE Products, Inc.

Product: Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt.…
Reason: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.
Published: March 15, 2017
Distribution: Nationwide

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

Data last updated: September 28, 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.