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All product recalls associated with Synovis Surgical Inovation Div. of.
Total Recalls
451
Past Year
40
Class I (Serious)
5
Most Recent
Sep 2025
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.
There is a potential for the pouch to become damaged during shipping, compromising the sterility of the device inside.
The bond may fail and a leak or separation of the device occur at the distal end (where this device connects to the arterial line).
Package Integrity/Sterility Compromised: The foil pouch in the Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement has a potential for minute defects which may compromise the sterility of the outside of the tray in which the device is packaged.