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Recall totals

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

37,139

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

State: MP ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 25, 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

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

FDA Recall Terminated Historical recordClass II

Temozolomide Capsules, 140 mg, packaged in a) 5-count bottles (NDC 0378-5263-98), b) 14-count bottles (NDC 0378-5263-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.

by Mylan LLC.

Reason: Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Temozolomide Capsules, 100 mg, packaged in a) 5-count bottles (NDC 0378-5262-98), b) 14-count bottles (NDC 0378-5262-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.

by Mylan LLC.

Reason: Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Albuterol Sulfate Inhalation Solution, USP, 0.021% (0.63 mg / 3 mL), 3mL Vials, Rx only, Mfd. for Watson Laboratories Inc., Corona, CA 92880 USA, Mfd. by Cipla Ltd. Verna, Goa India, NDC 0591-3467-53

by Actavis Inc

Reason: Failed Impurities/Degradation Specifications: Product is out of specification for a known degradant.
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL, NDC 0603-1147-56

by Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Reason: Failed Impurities/ Degradation Specifications
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC 0054-4297-31.

by Roxane Laboratories, Inc.

Reason: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint.
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Boulder Brands, LLC

Product: Earth Balance Vegan Cheddar flavored Mac and Cheese, 6oz pac…
Reason: Earth Balance Vegan White Cheddar flavored Mac and Cheese and Earth Balance Vegan Cheddar flavored Mac and Cheese with undeclared allergen, milk.
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Boulder Brands, LLC

Product: Earth Balance Vegan White Cheddar flavored Mac and Cheese, 6…
Reason: Earth Balance Vegan White Cheddar flavored Mac and Cheese and Earth Balance Vegan Cheddar flavored Mac and Cheese with undeclared allergen, milk.
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Schreiber Food International

Product: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce…
Reason: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.
Published: February 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

HCG (Chorionic Gonadotropin Lyopholized) II, 1000 unit vial, Rx only, Prepared by Town & Country, Compounding & Consultation Services, 106 Prospect St - 1st FL, Ridgewood, NJ 07459

by Town and Country Compounding and Consultation Services, LLC

Reason: Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.

by Sandoz Inc

Reason: Subpotent Drug: out of specification results for assay test.
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only, Manufactured by Perrigo, Yeruham, Israel, Distributed by Perrigo, Allegan, MI --- NDC 45802-736-84, UPC 345802736840

by L. Perrigo Company

Reason: Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets), NDC 69646-704-38 (10 ct. Carton of 1gm samples) / NDC 69646-704-01 (Individual 1gm Samples within Carton), Rx Only, Novum Pharma LLC, Chicago, IL 60654

by Novum Pharma, LLC

Reason: Subpotent Drug: Out of specification result for pramoxine hydrochloride
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Pentasa (mesalamine) Controlled-Release Capsules, 250 mg, 240 count bottle, Rx only, Manufactured for Shire US Inc., Lexington, MA --- NDC 54092-189-81

by Shire PLC

Reason: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles labeled to contain 250 mg capsules
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason: Failed Dissolution Specifications
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Herr Foods, Inc.

Product: Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.…
Reason: Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient . The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Herr Foods, Inc.

Product: Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 o…
Reason: Herrs Foods is announcing a product recall on Chipotle flavored Kettle Potato Chips under the Herrs and the Peddlers Pantry Brand, 2.625 oz., and 8.0 oz. due to possible health risk. These products were flavored with Chipotle seasoning that contained a milk ingredient. The milk ingredient is being recalled due to a potential risk of Salmonella contamination.
Published: January 25, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 30 mg over 9 hours (3.3 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5555-3.

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 20 mg over 9 hours (2.2 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5554-3.

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Transdermal Patch, 10 mg over 9 hours (1.1mg/hr), packaged in- 30 count per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc, Miami, FL 33186, NDC 68968-5552-3

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Out of Specification (OOS) results for the mechanical peel force (MPF) and and/or the z-statistic values.
Published: January 18, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Cytotec (misoprostol) Tablets, 200 mcg, 100 Tablets blister pack (10X10), For in-institution use only, Rx only, Distributed by G.D. Searle, Division of Pfizer, Inc., NY, NY --- NDC 0025-1461-34

by Pfizer Inc.

Reason: Failed Impurities/Degradations Specifications; Out of specification results for two known degradation products and total impurities at 18 months
Published: January 18, 2017
Distribution: Nationwide

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Data last updated: September 25, 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.