Ultraview DM3 91330-NRecalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

1 other recall cover devices cleared under the same FDA submission (K093802); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

1. Aug 13, 2024Open, Classified

   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.

   Z-3098-2024 · Root cause: Labeling design · Recall details · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K093802. One submission often covers many models, so check the product and lot details in each record.

• Z-2380-2012 · Jun 6, 2012 · Terminated
  Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3 Monitor is indicated for use by health care professionals for monitoring patient vital signs. The Ultravie