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Recall totals

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

37,266

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/pan-pepin-inc-emite-alerta-por-alergenos-en-el-producto-parabien-al-grano-debido-la-presencia-dePublished October 13, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 14, 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

Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-1318-3

by Apotex Corp.

Reason: Failed dissolution specifications.
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05

by Par Health USA, LLC

Reason: Crystallization
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe packaged in a carton, Rx only, Manufactured for: TerSera therapeutics LLC, Deerfield, IL 60015, BY: AstraZeneca UK Limited, Macclesfield, England, Product of Switzerland, website at www.zoladex.com, NDC 70720-950-36.

by TerSera Therapeutics LLC

Reason: Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08907, NDC 69238-2452-3.

by Amneal Pharmaceuticals, LLC

Reason: Defective Container; packets were found to be either empty or partially full.
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottle, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807. NDC: 27241-126-02

by Ajanta Pharma USA Inc

Reason: Failed Dissolution Specifications: below specification
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass I

TODD'S SEEDS LLC

Product: Todd's Seeds Variety Pack of Sprouting Seeds - Broccoli, Alf…
Reason: Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass I

TODD'S SEEDS LLC

Product: Todd's Seeds Alfalfa & Mung Bundle (1lb each), packaged sepa…
Reason: Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass I

TODD'S SEEDS LLC

Product: Todd's Seeds Salad Sprouting Mixture - Broccoli, Mustard, Al…
Reason: Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass I

TODD'S SEEDS LLC

Product: Todd's Seeds Sprouting Seed Mix - Broccoli, Radish, Alfalfa,…
Reason: Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass I

TODD'S SEEDS LLC

Product: Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccol…
Reason: Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass I

TODD'S SEEDS LLC

Product: Todd's Seeds Alfalfa Sprouting Seeds, packaged in heat-seale…
Reason: Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Published: October 7, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15

by Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Reason: Lack of Assurance of Sterility
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15

by Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Reason: Lack of Assurance of Sterility
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1685-1

by Amneal Pharmaceuticals of New York, LLC

Reason: Defective Delivery System: Possibility of no medication in the prefilled pen.
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ, 08540; Manufactured by: Macleods Pharmaceuticals, Ltd, Baddi, Himachal Pradesh, INDIA, NDC 33342-068-07.

by Macleods Pharmaceuticals Limited

Reason: Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification.
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops, Sterile, 0.5 FL OZ (15 mL) EACH, 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-02 (carton)

by Sterling Pharmaceutical Services LLC

Reason: Lack of Assurance of Sterility
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Lubricant Eye Drops-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494-448-05

by Sterling Pharmaceutical Services LLC

Reason: Lack of Assurance of Sterility
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38

by Sterling Pharmaceutical Services LLC

Reason: Lack of Assurance of Sterility
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

TRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL OZ (15 mL) bottles, Manufactured exclusively for TRP Company, Inc. 1575 Delucci Ln, Reno, NV 89502, NDC 17312-430-15.

by Sterling Pharmaceutical Services LLC

Reason: Lack of Assurance of Sterility
Published: September 30, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Reliable-1 Laboratories Lubricating Tears, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY, 11580, www.reliable1labs.com, NDC 69618-076-55.

by Sterling Pharmaceutical Services LLC

Reason: Lack of Assurance of Sterility
Published: September 30, 2026
Distribution: Nationwide

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Data last updated: October 14, 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.