Stryker Initiates Voluntary Product Recall of Modular-Neck Stems
MedSun: Newsletter #75, August 2012
FDA Medical Device Safety
Stryker has voluntarily recalled its Rejuvenate and ABG II modular-neck stems. Stryker has notified healthcare professionals and regulatory bodies of this voluntary recall. Patients who received a Rejuvenate Modular or ABG II modular-neck stem are encouraged to contact their surgeon. Patients uncertain if they have one of these products implanted should contact their surgeon or consult their medical records.
FDA Medical Device Safety. Stryker Initiates Voluntary Product Recall of Modular-Neck Stems Action Specific to Rejuvenate and ABG II Modular-Neck Stems. July 6, 2012.