Stripper, Vein, External
FDA adverse event reports and recall history for stripper, vein, external (product code DWQ), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 106
- Deaths
- 1
- Injuries
- 3
- Malfunctions
- 98
Reports per year
Source: FDA adverse event reports by year received, 2004–2025. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
- 2015-03-18TerminatedEmployee error
LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System is intended to provide a system to the removal of an incompetent greater saphenous vein. Catalog Number: 7210023, lot #61049252
Mislabeled with an incorrect expiration date
- 2007-08-02TerminatedOther
Smith & Nephew TRIVEX System Pneumatic Footswitch, Part #7209791; distributed by Smith & Nephew, Inc. - Endoscopy, Andover, MA 01810.
Build-up of static charge in Pneumatic Footswitch tubing may cause control unit to reset to default settings in the operating room during surgery.
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