Skip to main content
Get Alerts

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.

37,115
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 7,061–7,080 of 18,555 recalls

FDA Recall Terminated Historical recordClass II

Phendimetrazine Yellow Tabs 35mg, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: KVK-Tech, Newtown, PA 18940, NDC 0702-0077-10

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Topiramate 25mg Tabs White/round tablets, 10-count bags, Distributed by: Calvin Scott & Co., Inc. Alb., MN 87123, Mfg: Sun Pharm., Inc. Cranbury, NJ 08512, NDC 47335-0707-13

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Thyroid Neutral Tabs 2 gr, 28-count tablets, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, MN 87123, Manufactured by RLC, Cave Creek, AZ 85331 Labs, NDC 64727-3308-02

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Thyroid 1 Gr tablets, 28-count bags, Rx Only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by RLC Labs Cave Creek, AZ 85331, NDC 64727-3300-01

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Thyroid 1 Grain Tablets, 28-count bags, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by RLC Labs, Cave Creek, AZ 85331, NDC 64727-3300-02

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Hydrochlorothiazide 50mg tablets, 14-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Accord Healthcare, Inc., Durham NC 27703; NDC 16729-0184-17

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Hydrochlorothiazide (HCTZ) Orange Tabs 25mg, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123 Manufactured by Unichem Pharmaceuticals, NDC 29300-0128-10

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Hydrochlorothiazide 25mg tablets, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Mfg: Accord Healthcare, Inc, Durham, NC 27703, NDC 16729-0183-17

by Calvin Scott & Company, Inc.

Reason
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Prednisone Tablets, USP 2.5 mg, 100 tablets, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, Manufactured by: Tianjin Tianyao Pharmaceuticals Co., Ltd No. 221 Huanghai Road, Tianjin Economical-Technological Development Area, Tianjin, China 300457 NDC 0527-2931-37

by Lannett Company, Inc.

Reason
Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP 2.5 mg actually contained Prednisone Tablets, USP 10 mg
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Elitek (rasburicase) for injection, 7.5 mg vial, Rx Only Mfd. by Sanofi - Aventis U. S. LLC Bridgewater, NJ, 08807, NDC 0024-5151-75

by Sanofi-Aventis U.S. LLC

Reason
Failed Stability Specifications: Out of Specification result for enzyme activity levels noted during routine stability testing.
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

STIMATE (desmopressin acetate) Nasal Spray1.5 mg/mL, 2.5 mL glass vial with spray cap, Rx only, Manufactured for: CSL Behring LLC, King of Prussia, PA 19406-0901; By: Ferring GmbH, Kiel, Germany, NDC 0053-6871-00

by Ferring Pharmaceuticals Inc

Reason
Superpotent Drug
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Desmopressin Acetate Nasal Spray 10 mcg/0.1 mL, 5mL glass vial with spray cap, Rx only, Manufactured for: AMRING PHARMACEUTICALS INC., Berwyn, PA 19312, NDC 69918-501-05

by Ferring Pharmaceuticals Inc

Reason
Superpotent Drug
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

DDAVP Nasal Spray (desmopressin acetate) 10 mcg/0.1 mL, 5 mL bottles, Rx Only, Mfd for: Ferring Pharmaceuticals Inc., Parsippany, NJ 07054 USA, NDC 55566-2500-0

by Ferring Pharmaceuticals Inc

Reason
Superpotent Drug
Published
August 26, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Smith Foods Inc.

Product
Earth Grown brand Vanilla Non-Dairy Frozen Dessert in pint s…
Reason
Undeclared cashews in the product.
Published
August 26, 2020
Distribution
Products were distributed to the followi…

View recall →

FDA Recall United States Terminated Historical recordClass I

Smith Foods Inc.

Product
Earth Grown brand Chocolate Non-Dairy Frozen Dessert in pint…
Reason
Undeclared cashews in the product.
Published
August 26, 2020
Distribution
Products were distributed to the followi…

View recall →

FDA Recall United States Terminated Historical recordClass I

Smith Foods Inc.

Product
Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pi…
Reason
Undeclared cashews in the product.
Published
August 26, 2020
Distribution
Products were distributed to the followi…

View recall →

FDA Recall United States Terminated Historical recordClass II

High Liner Foods Inc.

Product
HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab…
Reason
Product contains undeclared hydrolyzed soy protein.
Published
August 26, 2020
Distribution
Multiple states

View recall →

FDA Recall Terminated Historical recordClass I

All Clean Hand Sanitizer, Fresh Scent, 1 Liter bottles, Ethyl Alcohol 70.00%, Produced by Eskbiochem SA de CV Ave Mexico Japon 50 Celaya, Gto. Mexico 38010, Distributed by All Clean Natural LTD, UPC Code 6 28055 37013 0

by Itech 361 LLC

Reason
Chemical Contamination: Product contains undeclared methanol.
Published
August 19, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Mibelas 24 Fe (norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets) chewable,1 mg/0.02 mg/75 mg, Rx Only, Provides 24 days of active therapy, Pouch Contains one wallet of 28 tablets, NDC: 68180-911-11, Carton contains 3 wallets of 28 tablets each, NDC: 68180-911-13, Distributed by: Lupin Pharmaceuticals, Inc., MD, 21200, Manufactured by: Lupin Limited, India.

by Lupin Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification result observed in related substance test.
Published
August 19, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Day & Night Pack Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles/Ear Itch MD Nighttime Intensive Soothing Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5

by Eosera, Inc.

Reason
cGMP Deviations.
Published
August 19, 2020
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.