Overview of recall records associated with Orthovita, Inc., dBA Stryker Orthobiologics., including dates, categories and classifications where available.
Classification mix: Class II: 4.
Two isolated instances of holes in the outer header bag component of the double barrier sterile packaging configuration
Several shipments of Vitagel product (a surgical hemostat) required to be stored at 2 -8 degrees Celsius (C) were not delivered to customers within the validated delivery time.
There is the potential for a breach in the inner or outer packaging pouches of all lots of the Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle.
There is the potential for a breach in the inner or outer packaging pouches of all lots of the Imbibe Bone Marrow Aspiration Needle.
This page summarizes recall records in which the official source identifies Orthovita, Inc., dBA Stryker Orthobiologics. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
