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 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.
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.
This recall is not part of a broader industry pattern.
The recall affects healthcare providers and patients relying on this kit for organ transplant procedures. Immediate action is necessary to prevent potential harm.
The Kit Code and Lot Numbers can typically be found on the product packaging or documentation.
Expect refunds or replacements to be processed within 4-6 weeks after submission.
Keep records of your purchase, correspondence with the manufacturer, and any photos of the product.
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.
Not sure what to do next? Our guide walks you through the process step by step.
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