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Recall totals

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

37,211

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

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 5, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

Temozolomide Capsules, 180 mg, packaged in a) 5-count bottles (NDC 0378-5264-98), b) 14-count bottles (NDC 0378-5264-14), 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, 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 II

PITTSBURGH SPICE & SEASONING CO

Product: Pittsburgh Spice Co; Buffalo Wing Sausage, 20.25 OZ for 25 #…
Reason: Pittsburgh Spice and Seasoning Company is voluntarily recalling Buffalo Wing And Sausage Seasoning because the milk powder ingredient was recalled by the ingredient manufacturer due to possible salmonella contamination.
Published: February 1, 2017
Distribution: OH and PA

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FDA Recall United States Terminated Historical recordClass I

Jem Raw Chocolate LLC

Product: Cashew Masala Tahini, Jem brand, 16 oz glass jar has UPC 8 6…
Reason: Cashew Masala Tahini is recalled due to a confirmed positive for Salmonella.
Published: February 1, 2017
Distribution: distributed in CA, FL, and OH.

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FDA Recall United States Terminated Historical recordClass I

Jem Raw Chocolate LLC

Product: Cashew Curry Tahini, Jem brand, 16 oz glass jar has UPC 8 61…
Reason: Cashew Curry Tahini, Jem brand, is recalled due to a confirmed positive for Salmonella.
Published: February 1, 2017
Distribution: distributed in CA, FL, and OH.

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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

Berner Food & Beverage, LLC

Product: Our Family Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NET 42…
Reason: Product contaminated with spoilage bacteria, Enterobacter cloacae and Pantoea species.
Published: February 1, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Berner Food & Beverage, LLC

Product: Roasted Garlic Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NE…
Reason: Product contaminated with spoilage bacteria, Enterobacter cloacae and Pantoea species.
Published: February 1, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Berner Food & Beverage, LLC

Product: Four Cheese Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NET 4…
Reason: Product contaminated with spoilage bacteria, Enterobacter cloacae and Pantoea species.
Published: February 1, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Berner Food & Beverage, LLC

Product: Creamy Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NET 425g;…
Reason: Product contaminated with spoilage bacteria, Enterobacter cloacae and Pantoea species.
Published: February 1, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Berner Food & Beverage, LLC

Product: Lite Creamy Alfredo, gluten free, Pasta Sauce; Glass jar, me…
Reason: Product contaminated with spoilage bacteria, Enterobacter cloacae and Pantoea species.
Published: February 1, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Tortillas Tita, LLC

Product: Tortilla Enchilada, 16 Oz. /16 units per case, packed in pla…
Reason: Tortillas Tita initiated a voluntary recall of all lots of their Corn Tortillas and Tortilla Enchilada produced between September 2016 and December 7, 2016, due to undeclared allergen Wheat.
Published: February 1, 2017
Distribution: Domestic: MI, OH Foreign: None VA/DO…

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FDA Recall United States Terminated Historical recordClass II

Tortillas Tita, LLC

Product: Corn Tortillas, 18 Count-16 Oz./453 g 16 units per case, 10…
Reason: Tortillas Tita initiated a voluntary recall of all lots of their Corn Tortillas and Tortilla Enchilada produced between September 2016 and December 7, 2016, due to undeclared allergen Wheat.
Published: February 1, 2017
Distribution: Domestic: MI, OH Foreign: None VA/DO…

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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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Data last updated: October 5, 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.