Pro-Med Instruments Gmbh: Medical Device Recalls in 2018

According to to data from the FDA, there were 3 medical device recalls made by Pro-Med Instruments Gmbh in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
• DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
• DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries