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

Recall Z-1287-2014 — 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.

U.S. FDA — Device Enforcement · United States · 2014-03-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1287-2014
Date of alert
2014-03-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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