Boston Scientific recalls Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN: M006185156080
- Recall date
- March 9, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1738-2020
- FDA classification
- Class II
- Brand / firm
- Boston Scientific
- Sold / distributed
- Nationwide Foreign: Europe, Middle East and Africa, the Americas (North America and South America, Asia Pacific and Japan
Why it was recalled
An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN: M006185156080
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