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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- AVID Medical
- Product type
- Transport Bag Kit
- Model numbers
- Kit Code: LIFE0080-01. UDI-DI: 10809160314500. Lot Number: 1650056. Expiration Date: 07/24/2028
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 2, 2026
Reported by FDA DEVICE
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
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
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
- Check the kit code: LIFE0080-01.
- Verify the UDI-DI: 10809160314500.
- 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.
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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
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Safety Guide
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