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

Recall Z-1716-2018 — BEQ-TOP 33700 ECC 3/8" PACK, Custom Tubing Pack with Bioline Coating, Catalog No. 701053845

U.S. FDA — Device Enforcement · United States · 2017-10-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1716-2018
Date of alert
2017-10-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Datascope Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
3000056811
Reported risk: The Better Bladder device provided as part of some custom tubing kits has been recalled by its manufacturer. Seal separation from the housing may allow air to enter the housing and collapse the balloon. This may increase resistance to flow in the venous line and cause a drop in ECMO circuit blood flow.
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.