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

Recall Z-2764-2020 — Captiflex Snares, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snares flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide minimal friction during extension

U.S. FDA — Device Enforcement · United States · 2020-07-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2764-2020
Date of alert
2020-07-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Boston Scientific Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08714729019411
Reported risk: BSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended would be a prolonged procedure duration, tissue damage and/or self-limited bleeding. The most severe potential injury would include immediate or delayed hemorrhage and/or perforation requiring intervention up to and including open surgery; the likelihood of these severe injuries occurring is remote and, to date, have not been reported as a complaint. The potential inability to cut may also lead to inadequate removal of target tissue.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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