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

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Source: FDA and USDA public dataLast updated September 16, 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 United States Terminated Historical recordClass II

Aroma Meats LLC

Product: Curry Leaf Powder (Karevepaku Podi), packaged in white plast…
Reason: Product was from unapproved source.
Published: January 26, 2022
Distribution: Distributed in Oregon.

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FDA Recall United States Terminated Historical recordClass II

Aroma Meats LLC

Product: Pulihora Paste is packaged in yellow plastic pouch. No weigh…
Reason: Product was from unapproved source.
Published: January 26, 2022
Distribution: Distributed in Oregon.

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FDA Recall United States Terminated Historical recordClass II

Aroma Meats LLC

Product: Cilantro Sweet Pickles (Kollimini Sweet) is packaged in Whit…
Reason: Product was from unapproved source.
Published: January 26, 2022
Distribution: Distributed in Oregon.

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FDA Recall United States Terminated Historical recordClass II

Aroma Meats LLC

Product: Nethili Pickle is packaged in clear plastic pouch and produc…
Reason: Fish pickled product is visible and the name Nethili is declared, but anchovy name is not declared on label.
Published: January 26, 2022
Distribution: Distributed in Oregon.

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FDA Recall United States Terminated Historical recordClass III

Aroma Meats LLC

Product: Fish-Pickle is packaged in yellow plastic pouch. No listed…
Reason: Fish is declared but specific fish name is not declared on Fish-pickle.
Published: January 26, 2022
Distribution: Distributed in Oregon.

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FDA Recall United States Terminated Historical recordClass II

Power Selles Imports dba Culinary Collective

Product: ZOCALO AJI LIMO DRIED CHILI PODS- ORGANIC, Dried Aji Peppers…
Reason: Due to presence of mold on product
Published: January 26, 2022
Distribution: Distributed in CA, KY, MO,MS, MT, NM, NY…

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FDA Recall Terminated Historical recordClass II

Sufentanil Citrate Injection, USP 100 mcg/2 mL (50 mcg/mL) for intravenous and epidural use, Rx only, 2 mL Ampule, Warning - May be habit forming, Preservative Free, Manufactured by Akorn, Inc. Lake Forest, IL 60045, NDC 17478-0050-02.

by Akorn, Inc.

Reason: Subpotent Drug: Out of specification for assay at the 30-month stability timepoint.
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Clobetasol Propionate Ointment USP, 0.05%, 60g tubes, Rx only, Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532. NDC 51672-1259-3

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Microbial Contamination of Non-Sterile Products: presence of R. Pickettii bacteria
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nitroglycerin Lingual Spray, 400 mcg per spray, 200 metered sprays, 12 g bottles, Rx only, Manufactured by Perrigo, Yeruham, Israel; Distributed by Perrigo, Allegan, MI 49010, NDC 45802-210-02

by Padagis US LLC

Reason: Defective Delivery System
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), 50 mL vials, Rx Only, Manufactured and Distributed by: Exela Pharma Sciences, LLC., Lenoir, NC 28645, NDC 51754-5001-1

by Exela Pharma Sciences LLC

Reason: Lack of Assurance of Sterility
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 --- NDC 50383-961-34

by Akorn, Inc.

Reason: Labeling: Missing Label
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles, Rx only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 -- NDC 50383-965-30

by Akorn, Inc.

Reason: Labeling: Missing Label
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Carbamazepine Tablets, USP 200 mg 100 Tablets Rx only NDC 13668-268-01 Manufactured by: Torrent Pharmaceuticals Ltd. Bharuch-392130, India Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920.

by Torrent Pharma Inc.

Reason: Failed Dissolution Specifications
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

The Natural Dentist Healthy Balance Peppermint Sage, Menthol 0.12%, 16.9 FL OZ (500 mL) bottles, Manufactured for Revive Personal Products Company, Madison, NJ 07940, UPC 7 14132 00071 4

by Revive Personal Products Company

Reason: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Menthol with UPC 7 14132 00071 4 instead of Peppermint Oil and Sage Oil with UPC 7 14132 00073 8
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Metoprolol Tartrate Tablets, USP 25 mg, 1000 - count bottle, Rx Only, Distributed by: TruPharma, LLC. Tampa, FL 33609; Manufactured by: Rubicon Research Prvate Limited Ambernath, Dist. Thane, 421506 India. NDC 52817-360-00

by Rubicon Research Private Limited

Reason: Complaint received of foreign matter (metal) embedded in tablet.
Published: January 19, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

NutraCap Labs LLC

Product: Wycked Naturals Wycked PRE Wycked Vice Strawberry Kiwi Sampl…
Reason: During an FDA investigation the firm was notified that the product contains undeclared milk.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

NutraCap Labs LLC

Product: Vyce World Nutrition Bed Burn Capsules 60ct Bottle NO UPC CO…
Reason: During an FDA investigation the firm was notified that the product contains undeclared milk.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

NutraCap Labs LLC

Product: UXO Supplements Ghillie Peach Mango 19oz Jar UPC CODE 6 3723…
Reason: During an FDA investigation the firm was notified that the product contains undeclared milk.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

NutraCap Labs LLC

Product: Tailor Made Compounding Clarity Capsule 90ct Bottle NO UPC C…
Reason: During an FDA investigation the firm was notified that the product contains undeclared milk.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

NutraCap Labs LLC

Product: Rare Planet Health Ageless Tropical Island Tropical Island 1…
Reason: During an FDA investigation the firm was notified that the product contains undeclared shellfish.
Published: January 19, 2022
Distribution: Product was shipped to the following sta…

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Data last updated: September 16, 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.