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

Recall Z-0090-2018 — Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number IPR-86/10 65 mL and Reservoir Bag for WalkMed Infusion Pump Part Number 204821 Catalog Number IPR-150/10 150 mL The WalkMed Reservoir Bag is designed for use with the WalkMed 350VL Ambulatory pump and is intended to be used a

U.S. FDA — Device Enforcement · United States · 2017-09-27 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0090-2018
Date of alert: 2017-09-27
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: WalkMed, LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20717525

Reported risk: There have been reported incidents of fluid leaks at the luer connection. Leaks have been confirmed to originate from, or near, the reservoirs clearcolored female luer connecter.

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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