BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of S4 FW258R K-Wire-Guidung Instrument for Set S4 SC from manufacturer Aesculap AG Tuttlingen

2009.01.13

Product group Medical instruments for use in humans
Reference 04786/08

The manufacturer Aesculap AG Tuttlingen recalls his medical device S4 FW258R K-Wire-Guidung Instrument for Set S4 SC. Due to insufficient material strenght the distal tip may break.

Recall of S4 FW258R K-Wire-Guidung Instrument for Set S4 SC from manufacturer Aesculap AG Tuttlingen , Download_VeroeffentlichtAm_EN PDF, 567KB, File does not meet accessibility standards