FDA recall record

Draegar Medical Systems The Infinity Acute Care System (IACS) Monitoring Solution with the recall — FDA Z-0258-2020

Cybersecurity vulnerabilities may cause device to reboot, lose alarm functionality, and/or lose communication with cockpit and/or the Infinity Network.

Class IIclassification
Z-0258-2020official record ID
Nov 6, 2019report date

Recall record at a glance

Official recordZ-0258-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmDraegar Medical Systems, Inc.
Report dateNov 6, 2019
Recall initiation dateSep 13, 2019
Quantity5634
LocationAndover, MA, United States

Official product description

The Infinity Acute Care System (IACS) Monitoring Solution with the Standalone Infinity M540 patient monitor. Model nos. MS25510, MS25520, MS26372.

Why the product was recalled

Cybersecurity vulnerabilities may cause device to reboot, lose alarm functionality, and/or lose communication with cockpit and/or the Infinity Network.

Distribution information

US Nationwide distribution.

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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