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All product recalls associated with Implant Innovations, Inc..
Total Recalls
4
Past Year
0
Class I (Serious)
0
Most Recent
Oct 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 nylon bag holding the product was not completely sealed before sterilization. Patients could be infected if the abutment is implanted.
The tray lid seals may be open thereby compromising the sterility barriers for the recalled lots.
Some 8mm OsseoFix drills included in the kit may be incorrectly laser marked as 4mm OsseoFix drills.