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All product recalls associated with Smith & Nephew, Inc. Endoscopy Division.
Total Recalls
154
Past Year
2
Class I (Serious)
0
Most Recent
Nov 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.
Product is non-sterile but labeled incorrectly as sterile.
Product is non-sterile but labeled incorrectly as sterile.
Surgical camera control units were not designed and manufactured to pass the IEC 60101 testing for electrical fast transients (EFT)