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Medline Nail Kit Recalled Over Sterility Concerns

Medline Industries recalled 1,640 units of its Nail Kit, Model POD14214, on January 5, 2026. The recall stems from concerns that the sterile saline wound wash may not meet required sterility standards. Patients and healthcare providers must stop using the product immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical Devices1) POD14214UDI-DI: 10889942819362(each)40889942819363(case)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 5, 2026
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
January 5, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries, LP
Product type
Wound Care Kit
Model numbers
1) POD14214, UDI-DI: 10889942819362(each), 40889942819363(case), Lot Number: 25CBS147, 2) POD14214, Lot Number: 25CBJ329, 3) POD14214, Lot Number: 25ABU209 +4 more
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 5, 2026

  2. Reported by FDA DEVICE

    March 4, 2026

  3. RecallRadar source check

    March 11, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter

About This Product

The Medline Nail Kit is designed for wound care and includes sterile saline for cleaning wounds. Consumers purchase this product to ensure proper hygiene and care of minor injuries.

Why This Is Dangerous

The recall is due to concerns that the saline solution may not have been manufactured to the required sterility assurance levels, risking contamination and infection.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers must stop using this product immediately to avoid potential health risks associated with using non-sterile wound care supplies.

Practical Guidance

How to identify if yours is affected

  1. Check the model number on the product packaging
  2. Verify the lot numbers against those listed in the recall
  3. Look for the UDI-DI number on the product

Where to find product info

The model number and lot numbers can typically be found on the packaging of the Nail Kit or on the instruction manual included with the product.

What timeline to expect

Refund processing may take 4-6 weeks after returning the recalled product.

If the manufacturer is unresponsive

  • Document all correspondence with Medline regarding the recall.
  • Follow up with Medline via phone or email if you do not receive a response.

How to prevent similar issues

  • Purchase products with clear sterility assurance labels.
  • Look for products that have been certified by health authorities.
  • Check for recalls regularly on the manufacturer’s website.

Documentation advice

Keep records of your purchase, including receipts and any correspondence related to the recall.

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Product Details

The recalled product is Medline's Nail Kit, Model Number POD14214. It was distributed worldwide, including the U.S., Bahamas, Bermuda, and Cayman Islands. The product was sold for an undisclosed price.

Key Facts

  • Recall date: January 5, 2026
  • Quantity recalled: 1,640 units
  • Affected model: POD14214
  • Hazard classification: Class II

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
1) POD14214
UDI-DI: 10889942819362(each)
40889942819363(case)
Lot Number: 25CBS147
2) POD14214
+7 more
Affected States
ALL
Report Date
March 4, 2026
Recall Status
ACTIVE

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