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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

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 30, 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).

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 Completed Historical recordClass III

Gildess FE 1/20 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, 6 blisters (NDC 0603-7609-17), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST PHARMACEUTICALS, USA, Huntsville, AL 35811

by Par Pharmaceutical, Inc.

Reason: Subpotent Drug; Ethinyl Estradiol
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall Completed Historical recordClass III

Gildess 1/20 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0,02 mg, USP), 21 count, (a) 3 blisters (NDC 0603-7607-48) and (b) 6 blisters (NDC 0603-7607-15), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST PHARMACEUTICALS, USA, Huntsville, AL 35811

by Par Pharmaceutical, Inc.

Reason: Subpotent Drug; Ethinyl Estradiol
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall Completed Historical recordClass III

Gildess 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP), 21 count, (a) 3 blisters (NDC 0603-7606-48) and (b) 6 blisters (NDC 0603-7606-15), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST PHARMACEUTICALS, USA, Huntsville, AL 35811

by Par Pharmaceutical, Inc.

Reason: Subpotent Drug; Ethinyl Estradiol
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia, BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 16252-570-30.

by Actavis Laboratories, FL, Inc.

Reason: Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17.
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Rikki USA, Inc.

Product: Hollandaise Sauce, sold as Sallere Classic Sauces and Butter…
Reason: Hollandaise Sauce was recalled due to presence of mold.
Published: November 9, 2016
Distribution: distributed in MD and OR.

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FDA Recall United States Terminated Historical recordClass I

Osage Gardens, Incorporated

Product: Organic 2oz Micro Greens. Clear Plastic Clamshell. Keep Refr…
Reason: Osage Gardens announces a voluntary recall of Organic 2oz Micro Greens due to a positive test for Salmonella.
Published: November 9, 2016
Distribution: Colorado and Kansas. No Canadian, VA/gov…

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FDA Recall United States Terminated Historical recordClass I

Vitalicious Acquisition

Product: VitaTops Apple Crumb, NET WT. 2 oz. (55g), packed in a clear…
Reason: The affected lots of VitaTops Apple Crumb contain undeclared milk.
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Roland Foods, LLC.

Product: Roland¿ Preserved Lemons, NET WT. 12.35 OZ., and Roland¿ PRE…
Reason: The product contains undeclared sulfites based on sampling and analysis by New York State Department of Agriculture and Markets and private laboratory testing.
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

JJBL LLC

Product: The Most Awesome Chocolate Bar Ever, Net wt. 1.5 oz. UPC 8 5…
Reason: The Most Awesome Chocolate Bar Ever is recalled due to undeclared wheat.
Published: November 9, 2016
Distribution: distributed in AK, AR, CA, CT, MD, NJ, N…

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FDA Recall United States Terminated Historical recordClass II

JJBL LLC

Product: The Stone Ground Peanut Butter Chocolate Bar, Net wt. 2.5 oz…
Reason: The Stone Ground Peanut Butter Chocolate Bar is recalled due to undeclared soy lecithin.
Published: November 9, 2016
Distribution: distributed in AK, AR, CA, CT, MD, NJ, N…

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FDA Recall Terminated Historical recordClass III

Invokamet (canagliflozin and metformin HCl) tablets, 150 mg/1,000 mg, 60-count bottle, Rx only, Finished product manufactured by: Janssen Ortho, LLC, Gurabo PR 00778, Manufactured for: Janssen Pharmaceuticals, Inc., Titusville, NJ 08560, NDC 50458-543-60

by Janssen Ortho L.L.C.

Reason: Labeling: Incorrect or Missing Package Insert - Xarelto prescribing information outserts may be affixed to the exterior of Invokamet bottles in place of the Invokamet prescribing information outsert.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

DIPYRIDAMOLE Tablets USP, 75 mg, 100-count bottle, Rx only, Dist. by: Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC 0054-0436-25

by Boehringer Ingelheim Pharmaceuticals, Inc.

Reason: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in a 75 mg Persantine 100-count bottle and 50 mg Persantine tablet was found in a 100 count bottle of 75 mg Dipyridamole.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Persantine (dipyridamole USP) tablets, 75 mg, 100-count bottles, Rx only, Dist. by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877, NDC 0597-0019-01

by Boehringer Ingelheim Pharmaceuticals, Inc.

Reason: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in a 75 mg Persantine 100-count bottle and 50 mg Persantine tablet was found in a 100 count bottle of 75 mg Dipyridamole.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Teal Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Purple Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Pink Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Silver Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color found to contain mold, yeast or bacteria
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Blue Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color found to contain mold, yeast, or bacteria
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Bob's Red Mill Natural Foods, Inc.

Product: Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM…
Reason: The firm is voluntarily recalling one lot of Guar Gum due to due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Brown Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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Data last updated: September 30, 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.