RecallRadar

FDA Device recall Z-2303-2012

Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278, 863279

On 2012-09-05 the FDA classified a Class II recall of Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278, 863279 by Philips Healthcare, citing philips SureSigns VSi/VS2+ patient monitors may not be properly secured and may fall from the wall mount.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2303-2012
ClassificationClass II
Statusterminated
Initiated2012-08-15
Published2012-09-05
Last updated2026-09-13 11:53 UTC
CompanyPhilips Healthcare
DistributionUS

Product

Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277, VS2+ 863278, 863279. The SureSigns VS2+ vital signs monitor is for monitoring, recording and alarming of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the monitor is intended for use in transport situations within a healthcare facility. The SureSigns VSi vital signs monitor is for measurement of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the monitor is intended for use in transport situations within a healthcare facility

Reason

Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and may fall from the wall mount

Identifiers

code_infoSerial Number Range CN14800101-CN14801360 CN21201362-CN21202440, CN21202525, SP13701043, USPP101007

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2303-2012%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.