Loading...
Loading...
All product recalls associated with Smith & Nephew, Inc. Endoscopy Division.
Total Recalls
559
Past Year
11
Class I (Serious)
11
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.
Mis-packaging-product in the package may be a different size than indicated on the labeling.
Mis-packaging-product in the package may be a different size than indicated on the labeling.
Smiths Medical became aware that product returned to them under recall # Z-0800-06/ Z-0807-06 was inadvertently distributed to consignees after the recall was initiated 03/29/2006. The product was originally recalled because Locator Wand covers, which are supplied on the outside of PORT-A-CATH and P.A.S. PORT sterile trays, may have an insufficient seal and product sterility could be compromised.