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

Recall Z-1104-2025 — Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each), Model: C-CA-23, Item: 33517;

U.S. FDA — Device Enforcement · Switzerland · 2024-12-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1104-2025
Date of alert
2024-12-19
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
New Medical Technologies Gmbh
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10381780171966
Reported risk: During the assembly of the cartridge to its connecting body part, the valve may open prematurely resulting in partial or complete emptying of the cartridge before its intended use.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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