BfArM - Federal Institute for Drugs and Medical Devices

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Product group Injections / Infusions / Transfusions / Dialysis - probes
Reference 07969/13

Teleflex extents the recall due to compromised primary packaging. Addditional device are included.

Teleflex extents a recall , Download_VeroeffentlichtAm_EN PDF, 349KB, File does not meet accessibility standards