Product Wiki · Recalls · U.S. FDA — Device Enforcement

Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environments and transport within a facility. — recall Z-0268-2018

U.S. FDA — Device Enforcement · United States · 2017-09-20 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0268-2018
Date of alert
2017-09-20
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Philips Electronics North America Corporation
Product category
device
Product type
Devices
Reported risk: Some SureSigns VSi, VS2+ products have the Date of Manufacture on its serial number label as %DoM , instead of the specific date in the format of YYYY-MM.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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