AVID Medical recalled 52 units of the ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17, on November 11, 2025. The devices are unsuitable for organ transplant procedures, presenting a serious health risk. Healthcare providers must stop using the device immediately and follow recall instructions.
Devices are not suitable for organ transplant.
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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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.
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.
This recall is not part of a broader industry pattern.
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.
The kit code and UDI can typically be found on the packaging of the product or in the user manual.
Expect a refund or replacement process to take approximately 4-6 weeks after contacting the manufacturer.
Keep records of all communications regarding the recall, including emails and notes from phone calls.
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.
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