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Recall totals

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

37,339

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,860

Class I recallsReasonable probability of serious health consequences

24,450

Class II recallsTemporary or medically reversible health consequences

2,901

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 2,095 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/imperio-distribution-llc-recalls-beef-jerky-products-produced-without-benefitPublished October 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 27, 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	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

FDA Recall OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 TerminatedTerminated: October 28, 2025Historical 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 TerminatedTerminated: February 17, 2026Historical 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 United States TerminatedTerminated: July 24, 2025Historical recordClass I

Harris Teeter

Product: ZENSHI HANDCRAFTED SUSHI California Roll 10pc (Brown Rice) N…
Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published: July 9, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: July 24, 2025Historical recordClass I

Harris Teeter

Product: ZENSHI HANDCRAFTED SUSHI Yuzu Teriyaki Tuna Roll 10pc Net Wt…
Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published: July 9, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: July 24, 2025Historical recordClass I

Harris Teeter

Product: ZENSHI HANDCRAFTED SUSHI Yuzu Teriyaki Sauce 3oz Net Wt. 3oz…
Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published: July 9, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: July 24, 2025Historical recordClass I

Harris Teeter

Product: ZENSHI HANDCRAFTED SUSHI Vegetable Roll 10pc (Brown Rice) Ne…
Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published: July 9, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: July 24, 2025Historical recordClass I

Harris Teeter

Product: ZENSHI HANDCRAFTED SUSHI Vegetable Roll 10pc Net Wt. 7.1oz U…
Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published: July 9, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: July 24, 2025Historical recordClass I

Harris Teeter

Product: ZENSHI HANDCRAFTED SUSHI Ultimate Chili Roll - Tuna 10pc Net…
Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published: July 9, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: July 24, 2025Historical recordClass I

Harris Teeter

Product: ZENSHI HANDCRAFTED SUSHI Ultimate Chili Roll - Shrimp Net Wt…
Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Published: July 9, 2025
Distribution: Product was shipped to the following sta…

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Data last updated: October 27, 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.