Print version of this report

Type of Product	Medical Device
TGA Recall Reference	RC-2017-RN-01263-1
Product Name/Description	SureSigns VSi, VS2+ SureSigns VSi - NBP Product Number: 863275 SureSigns VSi - NBP/SPO2 Product Number: 863276 SureSigns VSi - NBP/SPO2/Temp/Wireless Product Number: 863277 SureSigns VS2+ NBP/SPO2 Product Number: 863278 SureSigns VS2+ NBP/SPO2/Wireless Product Number: 863279 Multiple Serial Numbers ARTG Number: 93971
Recall Action Level	Hospital
Recall Action Classification	Class III
Recall Action Commencement Date	9/10/2017
Responsible Entity	Philips Electronics Australia Ltd
Reason/Issue	Philips has identified that certain 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.
Recall Action	Recall for Product Correction
Recall Action Instructions	1. Philips will provide affected customers with a new label with "Date of Manufacture" for each unit. An instruction will be provided to impacted customers on how to do the correction. 2. Philips Healthcare will contact customers impacted to arrange for the correction. This has been superseded by RC-2018-RN-00177-2 and as such has been closed out.
Contact Information	1800 251 400 - Philips Customer Care Centre