PlainRecalls
FDA Devices Moderate Class II Ongoing

Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331

Reported: September 18, 2024 Initiated: August 13, 2024 #Z-3099-2024

Product Description

Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331

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
1506 units
Distribution
awaiting additional details
Location
Topsfield, MA

Frequently Asked Questions

What product was recalled?
Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331. Recalled by Zoe Medical Incorporated. Units affected: 1506 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-3099-2024.