Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0210-2014 — Composite Series Skull Clamp, one clamp per tote. The MAYFIELD¿ Skull Clamp (A3059) is a cranial stabilization device, designed to provide rigid skeletal fixation. The Skull Clamp is placed on the patient's skull to hold their head and neck securely in a particular position when rigid fixation i

U.S. FDA — Device Enforcement · United States · 2013-08-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0210-2014
Date of alert
2013-08-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Integra LifeSciences Corp.
Product category
device
Product type
Devices
Reported risk: An investigation of an adverse trend of complaints for the Skull Clamp index locking knob not easily unlocking or disengaging and malfunctions of the 80 lbs. torque knob was initiated. None of the complaints resulted in a report of patient injury, adverse health consequence, or a delay / prolongation of the surgical procedure.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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