FDA recall record

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…

Class IIclassification
Z-3098-2024official record ID
Sep 18, 2024report date

Recall record at a glance

Official recordZ-3098-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmZoe Medical Inc.
Report dateSep 18, 2024
Recall initiation dateAug 13, 2024
Quantity6429 units
LocationTopsfield, MA, United States

Official product description

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

Why the product was 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.

Distribution information

awaiting additional details

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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