Quick Facts at a Glance
- Recall Date
- November 11, 2025
- Hazard Level
- HIGH
- Brand
- AVID Medical
- 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
- 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
- Organ Recovery Kit
- Model numbers
- Kit Code: LLOF1000-17, UDI : 10809160460726, Lot No : 1651709
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
November 11, 2025
Reported by FDA DEVICE
January 14, 2026
RecallRadar source check
January 21, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Devices are not suitable for organ transplant.
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 ORGAN RECOVERY OR PACK is designed for use in medical procedures for organ transplantation. Healthcare providers purchase these kits to ensure safe and sterile recovery of organs for transplant.
Why This Is Dangerous
The devices are deemed unsuitable for organ transplantation, which can lead to severe complications if utilized. This unsuitability poses a direct risk to patient health and safety during critical medical procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients and healthcare providers face immediate safety concerns due to the potential risks of using an unsuitable product. The inconvenience of returning the product and obtaining a replacement adds to the urgency of the situation.
Practical Guidance
How to identify if yours is affected
- Check if the kit code is LLOF1000-17.
- Verify the UDI number: 10809160460726.
- Look for Lot No: 1651709.
Where to find product info
The kit code and UDI can typically be found on the packaging of the product or in the user manual.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks after contacting the manufacturer.
If the manufacturer is unresponsive
- Document all communication attempts with AVID Medical.
- Consider contacting the FDA if the company is unresponsive.
How to prevent similar issues
- Always verify the suitability of medical devices for their intended use before purchase.
- Look for FDA approval and recall history when selecting medical devices.
- Consult with healthcare providers on the best products for specific medical needs.
Documentation advice
Keep records of all communications regarding the recall, including emails and notes from phone calls.
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Product Details
The recalled product is the ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17, with UDI 10809160460726 and Lot No: 1651709. It distributed nationwide, including states like Florida, Georgia, and Puerto Rico.
Key Facts
- Recall date: November 11, 2025
- Quantity recalled: 52 units
- Distribution: FL, GA, Puerto Rico
- Class I recall due to high hazard level
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Safety Guide
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