Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1736-2020 — Contour VL Ureteral Stent Set 6FX22-30CM with .035 Sensor UPN: M006180156080

U.S. FDA — Device Enforcement · United States · 2020-03-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1736-2020
Date of alert
2020-03-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Boston Scientific
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
24879999
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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