FDA recall record

Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor recall — FDA Z-1357-2026

Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.

Class IIIclassification
Z-1357-2026official record ID
Feb 18, 2026report date

Recall record at a glance

Official recordZ-1357-2026
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmSUREPULSE MEDICAL LTD
Report dateFeb 18, 2026
Recall initiation dateJan 20, 2023
QuantityN/A
LocationNottingham, N/A, United Kingdom

Official product description

Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor

Why the product was recalled

Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.

Distribution information

Worldwide - US Nationwide distribution in the states of CT, TX and the countries of United Kingdom of Great Britain and Northern Ireland, Netherlands, United Arab Emirates.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: N/A.

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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