Zoe Medical Spacelabs Ultraview DM3 Vital Signs Monitor recall — FDA Z-3098-2024
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.
Overview of recall records associated with Zoe Medical Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
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.
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.
This page summarizes recall records in which the official source identifies Zoe Medical Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.