Physio-Control recalls LIFEPAK CR2 defibrillators due to required inspections not being performed after servicing. Affected units have specific part numbers and serial codes. Consumers should contact the manufacturer for details.
Due to required inspections not being performed on products/units that have gone through servicing.
Physio-Control is recalling LIFEPAK CR2 defibrillators because required inspections weren't done after servicing. This could lead to improper function if the device isn't checked properly after maintenance.
The hazard occurs when required inspections after servicing are skipped, which could mean the defibrillator isn't working correctly. This might lead to improper treatment during emergencies if the device fails to function as intended.
Healthcare professionals who use the LIFEPAK CR2 defibrillator for emergency cardiac care are most at risk. The recall affects specific units with listed part numbers and serial codes.
Check for part numbers CR2-2-001451, catalog numbers 99512-001434, or UDI-DI code 883873785911 on the device. The recall includes specific units with the serial number 49638156.
Look for part numbers CR2-2-001451, catalog numbers 99512-001434, or UDI-DI code 883873785911 on the device.
The recall is due to required inspections not being performed on products after servicing, which could lead to improper function.
Affected units have part numbers CR2-2-001451, catalog numbers 99512-001434, UDI-DI code 883873785911, and serial number 49638156.
The recall does not specify a stop-use instruction; affected users should check device details and contact Physio-Control for further guidance.
We’ve drafted a message you can send Physio-Control to request your refund or repair — edit it as you like.
Subject: Recall Z-2499-2025 — Physio-Control Physio-Control Hello, I own a Physio-Control that is covered by recall Z-2499-2025 from Physio-Control. 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.
