BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall Pectus Table Top Bender, Biomet

Product group Medical instruments for use in humans
Reference 00351/08

The manufacturer Biomet Microfixation recalls Pectus Table Top Bender, reference number 01-3906. The bending procedure may potentially leave deep dents in the pectus bar. Affected lot numbers see English Advisory Notice.

Recall Pectus Table Top Bender, Biomet , Download_VeroeffentlichtAm_EN PDF, 52KB, File does not meet accessibility standards