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All product recalls associated with Ascension Orthopedics, Inc.
Total Recalls
3
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2009
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.
Trial product was larger than actual implant. Trial product was re-designed to more closely match the implant.
Screwdriver used with the Ascension Total Foot System not manufactured to specification, resulting in the driver not properly engaging and/or stripping the screws making it difficult to properly seat the screws during surgery.
Cracks in the tray due to excessive use can cause perforations in the outer wrap used to maintain instrument tray sterility.