FDA recall record

GE Healthcare Finland Oy GE Healthcare CARESCAPE Monitor B650 recall — FDA Z-2340-2018

When multiple CARESCAPE Monitor B650 units are connected to the same network and a network overload occurs for a prolonged time, the monitors may…

Class IIclassification
Z-2340-2018official record ID
Jul 11, 2018report date

Recall record at a glance

Official recordZ-2340-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGE Healthcare Finland Oy
Report dateJul 11, 2018
Recall initiation dateMay 25, 2018
Quantity69231 units
LocationHelsinki, Finland

Official product description

GE Healthcare CARESCAPE Monitor B650

Why the product was recalled

When multiple CARESCAPE Monitor B650 units are connected to the same network and a network overload occurs for a prolonged time, the monitors may simultaneously restart as designed. The monitor restart will not be completed until the network issue has been corrected.

Distribution information

worldwide

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

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