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All product recalls associated with Smith & Nephew, Inc. Endoscopy Division.
Total Recalls
1000
Past Year
631
Class I (Serious)
65
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.
Product is labeled as reusable but there is a potential that the cannulated handle of the product cannot be cleaned adequately following use.
Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.
Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.