Class II

Medical Device Recall: Spacelabs Ultraview DM3 Vital Signs Monitor (all variations -M, -MT, -N, -NT), Model Number 91330

Zoe Medical Incorporated · August 13, 2024

Reason for Recall

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.

Distribution

awaiting additional details

Quantity Affected

6429 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3098-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.