Health & Personal Care
HIGH
FDA DEVICE
DJO Surgical ALTIVATE Glenoid Reamer Head Recall Expands to 927 Units
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
DJO Surgical
Their is
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Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.