Defibtech recalls RMU-2000 Automated Chest Compression Devices with motor issues that may stop compressions, risking patient injury or death. Affected units have specific serial numbers.
Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or death.
Defibtech is recalling its RMU-2000 Automated Chest Compression Device because a motor problem could cause it to stop working during use. This might delay life-saving therapy and lead to injury or death if the device fails.
The device's motor may malfunction and stop compressions unexpectedly. This could delay life-saving treatment for someone in cardiac arrest, potentially causing injury or death if the device fails to operate when needed.
Users of the RMU-2000 device, particularly those in emergency medical settings or home use for cardiac emergencies, are at risk if the device stops compressions during critical moments.
Check the serial numbers listed in the recall notice: 502001000 through 502000999 (with specific numbers provided in the record). The device is sold under the brand Defibtech.
The device may stop compressions unexpectedly, risking patient injury or death. Do not use the device until you confirm it is safe.
The recall notice does not provide a specific recall number; it lists serial numbers for affected units.
Check the serial number on your device against the list of affected serial numbers provided in the recall notice (502001000 through 502000999).
The recall notice does not specify a return process; it only states the device should be stopped using immediately.
We’ve drafted a message you can send Defibtech to request your refund or repair — edit it as you like.
Subject: Recall Z-2543-2024 — Defibtech Defibtech Hello, I own a Defibtech that is covered by recall Z-2543-2024 from Defibtech. 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.
