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

Recall Z-0710-2014 — Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 9-12 mm Injects Above UPN: M00547100 The Extractor Pro XL Retrieval Balloon Catheter is used endoscopically to 1) remove stones from the biliary system; or 2) to facilitate injection of contrast medium while occluding the duct with the

U.S. FDA — Device Enforcement · United States · 2013-12-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0710-2014
Date of alert: 2013-12-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Boston Scientific Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 16231178

Reported risk: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive hole location or balloon size

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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