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All product recalls associated with Smith & Nephew, Inc. Endoscopy Division.
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
Most Recent
Jan 2026
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.
Sterility seal of the package tray may have gaps/voids compromising the sterility of the device.
The sterility seal of the package trays may have incomplete seals compromising the sterility of the device
Teleflex Medical has identified that the product may malfunction, causing the handle to heat up. There is a potential for the heated handle to burn the user.