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

Recall Z-1495-2025 — Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only

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-1495-2025
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): 04048675389620

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

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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