AVID Medical recalled 132 units of its Organ Recovery Kit on November 11, 2025. The devices are not suitable for organ transplant, posing a high risk to patients. Healthcare providers and patients should 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 Kit, Kit Code: LLOG1000-15. It was distributed nationwide in Florida, Georgia, and Puerto Rico. The affected lot numbers are 1632138 and 1648393.
The Organ Recovery Kit is unsuitable for organ transplant. This defect poses a high risk, potentially affecting patient safety during medical procedures.
No specific incidents of injury or death have been reported at this time. The recall is classified as Class I due to the high hazard level.
Stop using the Organ Recovery Kit immediately. Contact AVID Medical or your healthcare provider for instructions on returning the product.
For further information, contact AVID Medical, Inc. via email. Additional details are available at the FDA recall notice link.
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