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

Recall Z-2766-2015 — Boston Scientific, WATCHMAN Access System Access Sheath with Dilator, 14F Single curve( M635TU10060, TU1006) , 14F Double curve (M635TU20060, TU2006) , & 14F Anterior curve (M635TU40060, TU4006). For cardiac use.

U.S. FDA — Device Enforcement · United States · 2015-08-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2766-2015
Date of alert
2015-08-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Boston Scientific Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
15611295
Reported risk: Cross-threading of the hemostasis valve may occur if it is tightened with the dilator in place, possibly preventing subsequent sealing of the valve when desired. This Field Correction reinforces the Directions for Use (DFU) and gives further guidance on correct use of the hemostasis valve to avoid cross-threading and to securely seal the valve, minimizing potential for undesired blood leakage.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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