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Recall totals

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

37,061

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 10, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical recordClass II

Metoprolol Succinate Extended-Release Tablets, USP, 25 mg, Packaged in a) 100-count bottle, NDC 70010-780-01; b) 500-count bottle, NDC 70010-780-05; Rx only, Manufactured by: Granules India Limited, Hyderadab-500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA 20151,

by Granules Pharmaceuticals Inc.

Reason: Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA, Distributed by Cardinal Health, Dublin, OH 43017, NDC 55154-3363-0

by The Harvard Drug Group LLC

Reason: Defective container; blister packaging inadequately sealed.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10), blister pack cartons, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA, NDC 0904-6665-61

by The Harvard Drug Group LLC

Reason: Defective container; blister packaging inadequately sealed.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton, Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA. UPC CODE 3 10310 40000 2.

by Church & Dwight Inc

Reason: Microbial Contamination of Non-Sterile Products: Fungal contamination of infant oral swabs.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6

by Church & Dwight Inc

Reason: Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5

by Church & Dwight Inc

Reason: Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL), For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative Free, 10mL Sterile Single-Dose Vial, Rx Only, Medivant Healthcare, 158 S. Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0001-0.

by Tailstorm Health INC

Reason: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LIDOcaine HCL Sterile Injection, USP, 100mg/10mL, 1%, (10mg/mL), w/EPINEPHRINE 1:100,000, For Infiltration & Nerve Block, Including Caudal & Epidural Use, 10 mL Sterile Single-Dose Vial, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 85226, NDC 81483-0037-0.

by Tailstorm Health INC

Reason: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

KETAmine Hydrochloride Injection, USP, 500mg/5mL, (10mg/mL), For IM or Slow IV Use, 5mL Sterile Multi-Dose Vial, Rx Only, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 85226, NDC 81483-0007-2.

by Tailstorm Health INC

Reason: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office Use Only, Compounded Durg by: Medivant Healthcare, 158 S. Kyrene Rd. Chandler, AZ 85226, NDC 81483-0006-0.

by Tailstorm Health INC

Reason: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

BUPIVAcaine HCL Sterile injection, USP w/EPINEPHRINE 1:200,000, 50 mg/10mL, 0.5%, (5mg/mL), 10 mL Sterile Single-Dose Vial, Rx Only, For Nerve Block, Caudal & Epidural Anesthesia Only, Warning: Contains Sulfites, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0036-0.

by Tailstorm Health INC

Reason: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LIDOcaine HCl Injection, USP, 10mg/mL, 1% (100 mg/10mL), 10 mL Sterile Single Dose Vial, Rx Only, For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative-Free, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0000-0.

by Tailstorm Health INC

Reason: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Vita Warehouse Corp.

Product: 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jens…
Reason: Contains undeclared peanut
Published: July 9, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass I

August Egg Company

Product: --- Shell Eggs; Brown; Various sizes - medium, large, and ju…
Reason: Potential contamination with Salmonella.
Published: July 9, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Peak Cocktails

Product: Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans s…
Reason: Overpressurization leading to exploding cans
Published: July 9, 2025
Distribution: Product was distributed to consumers in:…

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FDA Recall Ongoing Historical recordClass II

Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5%, 15 mL, Rx Only, Sterile, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-0589-3

by Apotex Corp.

Reason: Lack of Assurance of Sterility
Published: July 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Azelastine HCl Ophthalmic Solution, USP, 0.05%, 6 mL, Rx Only, Sterile, Mfg. by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Mfg. for: Apotex Corp., Weston, FL 33326, NDC 60505-0578-4

by Apotex Corp.

Reason: Lack of Assurance of Sterility
Published: July 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 10 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-1003-2

by Apotex Corp.

Reason: Lack of Assurance of Sterility
Published: July 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and further packaged 24 per case, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC 0264-7800-10.

by B BRAUN MEDICAL INC

Reason: Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.
Published: July 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

0.9% Sodium Chloride Injection, USP, Flexible Plastic Container, Rx Only Fresenius Medical Care North America, Waltham, MA 02451, 1-800-323-5188, NDC 49230-300-10

by Fresenius Medical Care Holdings, Inc.

Reason: Lack of Assurance of Sterility
Published: July 2, 2025
Distribution: Nationwide

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Data last updated: September 10, 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.