HIGH

AVID Medical Recalls Transport Bag Kit Over Sterility Risk

AVID Medical recalled 1,500 units of the TRANSPORT BAG KIT on January 2, 2026. A seal issue with the Tyvek bag may compromise the sterility of the kit. The recall affects healthcare providers and patients in New Jersey.

Quick Facts at a Glance

Recall Date
January 2, 2026
Hazard Level
HIGH
Brand
AVID Medical
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Tyvek bag seal issue which may compromise sterility of the kit.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact AVID Medical, Inc. or your healthcare provider for instructions. Notification method: E-Mail

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About This Product

The Halyard TRANSPORT BAG KIT is designed for medical transport and storage of sterile products. Healthcare providers use these kits to ensure patient safety during procedures.

Why This Is Dangerous

The Tyvek bag seal issue can compromise the sterility of the kit, increasing the risk of infections for patients who rely on sterile medical equipment.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

This recall affects healthcare providers and patients in New Jersey, creating urgency for immediate action to prevent potential health risks.

Practical Guidance

How to identify if yours is affected

  1. Check the kit code: LIFE0080-01.
  2. Verify the UDI-DI: 10809160314500.
  3. Look for the Lot Number: 1650056.

Where to find product info

The kit code, UDI-DI, and Lot Number can typically be found on the packaging or the product label.

What timeline to expect

Expect a timeline of 4-6 weeks for refund processing once the recall is initiated.

If the manufacturer is unresponsive

  • Contact the manufacturer again to follow up on your request.
  • File a complaint with the FDA if you receive no response.

How to prevent similar issues

  • When purchasing medical devices, always check for FDA approvals and recalls.
  • Look for sterility indicators on packaging when buying medical kits.

Documentation advice

Keep copies of any correspondence with the manufacturer and take photographs of the product.

Product Details

The recalled product is the Halyard TRANSPORT BAG KIT, Kit Code: LIFE0080-01, with UDI-DI: 10809160314500 and Lot Number: 1650056. The expiration date is July 24, 2028. The kits were distributed nationwide, primarily in New Jersey.

Key Facts

  • Recall date: January 2, 2026
  • FDA classification: Class II
  • Quantity recalled: 1,500 units
  • Distribution: New Jersey

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
Kit Code: LIFE0080-01. UDI-DI: 10809160314500. Lot Number: 1650056. Expiration Date: 07/24/2028
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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