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All product recalls associated with Smith & Nephew, Inc., Endoscopy Div..
Total Recalls
37
Past Year
0
Class I (Serious)
0
Most Recent
Sep 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.
Device may have improper Laser Marking, 4mm device may be marked as 6mm and 6mm device may be marked as 4mm.
Device may have improper Laser Marking, 4mm device may be marked as 6mm and 6mm device may be marked as 4mm.
Device may have improper Laser Marking, 4mm device may be marked as 6mm and 6mm device may be marked as 4mm.