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All product recalls associated with Stryker Instruments, Instruments Div..
Total Recalls
3
Past Year
0
Class I (Serious)
0
Most Recent
Jul 2004
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The tracker is not locking adequately to the anchoring pin, resulting in unacceptable movement, which will affected the patient tracker system.
Product sterility may have been compromised by an inadequate package seal.
Non-sterilized product sold as sterile.