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.

Additional Information:

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.
http://www.fda.gov/Safety/Recalls/ucm311043.htm


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