OrganOx recalls metra liver transport devices with serial numbers 511-537 for potential battery cell damage causing short circuits. Affected units may require repair or replacement to prevent electrical hazards during liver transport.
Battery movement led to damage of one of the battery cells causing it to short to the battery retention bracket
OrganOx is recalling specific metra liver transport devices that could have battery cell damage leading to short circuits. This risk could cause electrical issues during liver transport procedures, potentially affecting organ preservation.
Battery movement during use can damage one of the battery cells, causing it to short to the battery retention bracket. This short circuit may lead to electrical issues that could compromise liver preservation during transport.
Healthcare professionals using OrganOx metra devices for donor liver transport are most at risk. Affected units have specific serial numbers listed in the recall.
Check if your OrganOx metra device has a serial number between 511 and 537 (inclusive). The device is used for transporting donor livers for transplantation.
Verify your OrganOx metra device's serial number to see if it is listed in the recall range (511-537).
Reach out to OrganOx directly for guidance on next steps if your device is affected.
Battery movement can damage one of the battery cells, causing it to short to the battery retention bracket.
Serial numbers 511, 512, 514, 515, 516, 517, 518, 519, 520, 522, 523, 524, 525, 527, 528, 529, 530, 531, 533, 535, 536, 537.
The recall does not require immediate stoppage; affected devices may be used with caution after contacting OrganOx.
We’ve drafted a message you can send OrganOx to request your refund or repair — edit it as you like.
Subject: Recall Z-0501-2025 — OrganOx OrganOx Hello, I own a OrganOx that is covered by recall Z-0501-2025 from OrganOx. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
