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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

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

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Source: FDA and USDA public dataLast updated September 17, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

BUP 10MG/HYDROM 15MG/SUF 200MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BUP 10MG/ FENT 1000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BACLOFEN 2000MCG/ML (40) INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BAC 800MCG/BUP 6.7MG/CLON 600 MCG/FENT 850MCG/MORP 20MG INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BAC 250MCG/ /FENT 3500MCG/ /MORP 25MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BAC 2400MCG/ FENT 2600MCG/ MORP 3600MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

BAC 160MCG/HYDROM 16MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Dutasteride Capsules, 0.5 mg, 30 Capsules (6 X 5) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-282-13.

by AVKARE Inc.

Reason: Failed Impurities/Degradation Specifications: High out of specification results for related compounds.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Bob's Red Mill Natural Foods, Inc.

Product: Garbanzo Beans or Chickpeas, sold under brand Bob's Red Mill…
Reason: Product is recalled due to the potential presence of glyphosate.
Published: January 22, 2020
Distribution: Garbanzo Beans were distributed in CA, C…

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FDA Recall United States Terminated Historical recordClass III

Bob's Red Mill Natural Foods, Inc.

Product: 13 Bean Soup Mix is sold under Bob's Red Mill brand, packag…
Reason: Product is recalled due to the potential presence of glyphosate.
Published: January 22, 2020
Distribution: Garbanzo Beans were distributed in CA, C…

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FDA Recall Terminated Historical recordClass III

SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5513-2 UPC 8 83484 71794 3 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason: Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5514-1 UPC 8 83484 717936 6 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason: Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deodorant Net Wt 2.6 oz (73g) NDC# 41595-5547-1 UPC 8 83484 31020 5 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason: Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC 8 83484 71717 2 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason: Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets 75mg), Rx Only, Distributed by: Lupin Pharmaceuticals Inc Baltimore, MD 21202, Manufactured for: Lupin Limited Pithampur 454775 INDIA 240875, NDC 68180-866-11

by Lupin Pharmaceuticals Inc.

Reason: Failed Tablet/Capsule Specifications: Complaints related to crumbling of tablets when popped out of the blister pack.
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Reichel Foods Inc.

Product: Pro2Snax To The Max snack tray containing Sweet Gala Apples,…
Reason: Products are being recalled due to Listeria monocytogenes contamination.
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Reichel Foods Inc.

Product: Pro2Snax To The Max snack tray containing Sliced Apples, Har…
Reason: Products are being recalled due to Listeria monocytogenes contamination.
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wayfare Health Foods LLC

Product: Plant Based WayFare Butterscotch Pudding Organic Dairy Free,…
Reason: Product is recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wayfare Health Foods LLC

Product: Plant Based WayFare Vanilla Pudding Organic Dairy Free, Item…
Reason: Product recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published: January 15, 2020
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wayfare Health Foods LLC

Product: Plant Based WayFare Chocolate Pudding Organic Dairy Free, It…
Reason: Product recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published: January 15, 2020
Distribution: Nationwide

View recall →

Data last updated: September 17, 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.