Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
DORO LUCENT Transitional Member Recalled by Pro-Med Instruments Gmbh Due to The combination of two different design revisions of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pro-Med Instruments Gmbh directly.
Affected Products
DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
Quantity: 31 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 7 states: CA, GA, MS, OH, TN, TX, WV
About Pro-Med Instruments Gmbh
Pro-Med Instruments Gmbh has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report