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Recall totals

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

37,268

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 16, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall Ongoing2026 recordClass II

Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 51672-4206-6

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC 57511-0611-1.

by Elevate Oral Care

Reason: sub potency
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Ltd, Sangareddy -502313, Telangana, India, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, NDC 31722-813-60.

by Annora Pharma Private Limited

Reason: Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass I

BD ChloraPrep FREPP Clear,(2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)) 1.5 mL Applicator, 20 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-30.

by CareFusion 213, LLC

Reason: Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass I

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 1 mL Applicator, 60 Applicators per inner Carton, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-31.

by CareFusion 213, LLC

Reason: Non-Sterility: Due to presence of Aspergillus penicillioides.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

BD ChloraPrep FREPP Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) 1.5 mL Applicator, 20 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-30.

by CareFusion 213, LLC

Reason: Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) 1 mL Applicator, 60 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-31.

by CareFusion 213, LLC

Reason: Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

hydrOXYzine Hydrochloride Oral Solution, USP, 10 mg/5 mL, 473 mL (1 Pint), Rx only, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623. NDC: 70954-912-10

by ANI Pharmaceuticals, Inc.

Reason: Presence of foreign substance
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC 61919-482-60), 60 Caps; CYMBALTA, Packaged and Distributed by Direct Rx.

by Direct Rx

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Sensipar (cinacalcet) Tablets, 90mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks, CA 91320-1799, Made in Japan. NDC 55513-075-30

by Amgen, Inc.

Reason: CGMP Deviations
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC 55513-810-60

by Amgen, Inc.

Reason: Presence of Foreign Substance.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-074-30

by Amgen, Inc.

Reason: CGMP Deviations
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Sensipar (cinacalcet) Tablets, 30mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-073-30

by Amgen, Inc.

Reason: CGMP Deviations
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy.

by Amgen, Inc.

Reason: Presence of Foreign Substance.
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ 08807, NDC 27241-120-04.

by Ajanta Pharma USA Inc

Reason: CGMP Deviations
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, in 46268, NDC 0904-7282-10. Blister Label: Methylergonovine Maleate Tablets, 0.2 mg, USP, One Tablet, Major Pharm/Indianapolis, IN 46268, NDC 0904-7282-10.

by The Harvard Drug Group LLC

Reason: Subpotent Drug
Published: July 1, 2026
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 10, 20262026 recordClass I

George J Howe Company, Inc.

Product: 25# Sunflower Seeds C/S
Reason: The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Published: July 1, 2026
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: September 10, 20262026 recordClass I

George J Howe Company, Inc.

Product: 5# Sunflower Seeds C/NS
Reason: The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Published: July 1, 2026
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: September 10, 20262026 recordClass I

George J Howe Company, Inc.

Product: 5# Sunflower Seeds C/S
Reason: The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Published: July 1, 2026
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: September 10, 20262026 recordClass I

George J Howe Company, Inc.

Product: 8/9.5oz Tub Nut - Sunflower Seed
Reason: The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Published: July 1, 2026
Distribution: The recalled product was distributed to…

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Data last updated: October 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.