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

Recall Z-3098-2024 — Spacelabs Ultraview DM3 Vital Signs Monitor (all variations -M, -MT, -N, -NT), Model Number 91330

U.S. FDA — Device Enforcement · United States · 2024-08-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3098-2024
Date of alert
2024-08-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zoe Medical Incorporated
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00851920007002
Reported risk: This product labeling does not adequately provide warning about the risks associated with the use of damaged batteries or batteries past the intended use life.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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