Quick Facts at a Glance
- Recall Date
- November 11, 2025
- 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
- Organ Recovery Kit
- Model numbers
- Kit Code: LLOG1000-15, UDI: 10809160432679, Lot No: 1632138, Lot No: 1648393
- Sold at
- Unknown
- 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 Kit by AVID Medical is used in surgical procedures related to organ transplant. Healthcare providers and surgical teams rely on this kit for safe and effective organ recovery.
Why This Is Dangerous
The product's unsuitability for organ transplant presents a significant risk during vital surgical procedures. Using an unsuitable kit can compromise patient safety and transplant success.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects healthcare providers and patients relying on this kit for organ transplant procedures. Immediate action is necessary to prevent potential harm.
Practical Guidance
How to identify if yours is affected
- Check the Kit Code: LLOG1000-15.
- Verify the Lot Numbers: 1632138 and 1648393.
- Look for the UDI: 10809160432679.
Where to find product info
The Kit Code and Lot Numbers can typically be found on the product packaging or documentation.
What timeline to expect
Expect refunds or replacements to be processed within 4-6 weeks after submission.
If the manufacturer is unresponsive
- Document all communications regarding the recall.
- Follow up with AVID Medical if no response is received within a week.
- Consider contacting regulatory authorities if issues persist.
How to prevent similar issues
- Always check for recalls on medical devices before use.
- Look for FDA approval and certifications when purchasing medical devices.
- Consult healthcare providers for recommendations on safe products.
Documentation advice
Keep records of your purchase, correspondence with the manufacturer, and any photos of the product.
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
Product Details
The recalled product is the Organ Recovery Kit, Kit Code: LLOG1000-15. It was distributed nationwide in Florida, Georgia, and Puerto Rico. The affected lot numbers are 1632138 and 1648393.
Key Facts
- Unsuitable for organ transplant
- Class I recall
- Nationwide distribution in FL, GA, Puerto Rico
- Immediate action required
Browse More Recalls
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 ProductGet Alerts for Health & Personal Care Recalls
Get instant alerts for recalls that affect you. Free forever.