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 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.
These devices are deemed unsuitable for organ transplants, posing a significant risk to patient safety. The recall falls under Class I, indicating a high hazard level.
Patients and healthcare providers should stop using the device immediately. Contact AVID Medical, Inc. or your healthcare provider for further instructions.
For more information, reach AVID Medical, Inc. via email. More details can be found on the FDA website.
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