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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: AS ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 24, 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

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

Aid Backpack Kit - Product Code 85-0917, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amphibious Trauma Kit - Product Code 85-0639, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit - Product Code 85-1274, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue

by North American Rescue LLC.

Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION, 62.5mg elemental iron/5mL, 10 (5mL vials) per shelf pack, Rx only, Mfd: Hikma Farmaceutica (Portugal,) SA Distributed by: Westward Eatowntown NJ 07724 USA, Shelf pack NDC 0143-9570-10, Unit dose NDC 0143-9570-01

by West-Ward Pharmaceuticals Corp.

Reason: Subpotent Drug: Product has an an out of specification in iron assay analysis found during 18 month stability testing.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg, 50 Metered Sprays, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044, By: 3M Drug Delivery Systems, Northridge, CA 91324, NDC 59310-210-13.

by Teva Pharmaceuticals USA

Reason: Failed Content Uniformity: Product was out of specification for spray content uniformity obtained during stability testing.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Qnasl (beclomethasone dipropionate) Nasal Aerosol 40 Mcg, 60 Metered Sprays, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044, By: 3M Drug Delivery Systems, Northridge, CA 91324, NDC 59310-206-06 and 59310-206-08 (Physician Samples).

by Teva Pharmaceuticals USA

Reason: Failed Content Uniformity: Product was out of specification for spray content uniformity obtained during stability testing.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Perfetti Van Melle USA Inc

Product: Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz…
Reason: Blood was observed on equipment during packaging.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

To Your Heart's Content

Product: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk…
Reason: Undeclared allergen of milk from the declared ingredient coconut cream powder.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mondelez International

Product: Nabisco Oreo Fudge Creme Mint Variety, Net Wt. 11.3 oz Dist…
Reason: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and mint varieties) due to milk allergen not being declared on the ingredient list.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mondelez International

Product: Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz…
Reason: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and mint varieties) due to milk allergen not being declared on the ingredient list.
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

4 C Foods, Corp.

Product: Cento Romano Grated Cheese, UPC 70796-90501, 6 oz
Reason: FDA sample revealed the presence of Salmonella contamination
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

4 C Foods, Corp.

Product: Cento Parmesan Grated Cheese, UPC 70796-90502, 6 oz
Reason: FDA sample revealed the presence of Salmonella contamination
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

4 C Foods, Corp.

Product: 4C Homestyle All Natural 100% Imported Italian Pecorino Roma…
Reason: FDA sample revealed the presence of Salmonella contamination
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

4 C Foods, Corp.

Product: 4C Homestyle All Natural Parmesan/Romano Grated Cheese, UPC…
Reason: FDA sample revealed the presence of Salmonella contamination
Published: December 14, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

4 C Foods, Corp.

Product: 4C Homestyle All Natural Parmesan Grated Cheese, UPC 41387-3…
Reason: FDA sample revealed the presence of Salmonella contamination
Published: December 14, 2016
Distribution: Nationwide

View recall →

Data last updated: September 24, 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.