BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of PROPAQ LT Patient Monitors from WelchAllyn

Product group Medical electronics / Electromedical devices
Reference 03248/06

WelchAllyn has issued an information about the recall of PROPAQ LT Patient Monitors with serial numbers KA001225 - KA002847. In the 1. failure case the pulse oximetry sensors may emit sufficient heat through its LEDs to burn the finger of a patient.

Recall of PROPAQ LT Patient Monitors from WelchAllyn , Download_VeroeffentlichtAm_EN PDF, 103KB, File does not meet accessibility standards