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

Recall Z-1493-2025 — Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is intended for single us

U.S. FDA — Device Enforcement · United States · 2025-03-12 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1493-2025
Date of alert: 2025-03-12
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Draeger, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 04048675248996

Reported risk: The potential for cracks forming in the breathing circuit hose.

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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