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

Recall Z-3329-2018 — CONTI ECHO CT W/2IN TUOHY ULTRA 360 SET, Material Number 331767 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter

U.S. FDA — Device Enforcement · United States · 2018-07-20 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-3329-2018
Date of alert: 2018-07-20
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: B. Braun Medical, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 61615716

Reported risk: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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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