PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: September 18, 2024 Initiated: August 13, 2024 #Z-3098-2024

Product Description

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

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.

Details

Recalling Firm
Zoe Medical Incorporated
Units Affected
6429 units
Distribution
awaiting additional details
Location
Topsfield, MA

Frequently Asked Questions

What product was recalled?
Spacelabs Ultraview DM3 Vital Signs Monitor (all variations -M, -MT, -N, -NT), Model Number 91330. Recalled by Zoe Medical Incorporated. Units affected: 6429 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 18, 2024. Severity: Moderate. Recall number: Z-3098-2024.