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Pro-Med Instruments Recalls
5 recalls on record · December 13, 2017 to June 4, 2025 · Medical Devices
Recalls by year
17
18
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 4, 2025Medical DevicesFDA
Pro-Med Instruments Gmbh recalls DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
Hazard: Potential of compromised compatibility resulting in influence on the positioning of the reference array and an influence of the function of the navigation system cannot be excluded.
September 26, 2018Medical DevicesFDA
Pro-Med Instruments Gmbh recalls DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies
Hazard: The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and Transitional Member within one set up might lead to a malfunction and failure of the headrest system.
September 26, 2018Medical DevicesFDA
Pro-Med Instruments Gmbh recalls DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous cranio
Hazard: The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and Transitional Member within one set up might lead to a malfunction and failure of the headrest system.
September 26, 2018Medical DevicesFDA
Pro-Med Instruments Gmbh recalls DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
Hazard: The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and Transitional Member within one set up might lead to a malfunction and failure of the headrest system.
December 13, 2017Medical DevicesFDA
Pro-Med Instruments Gmbh recalls pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box), S
Hazard: The firm received reports of two breakages of the pin tips which occurred during two identical surgery procedures. The breakage occurred at the very distal end of the conical part of the skull pin tip.