Philips Electronics North America Corporation: Medical Device Recall in 2017 - (Recall #: Z-0268-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environments and transport within a facility.

Product Classification:

Class III

Date Initiated: September 20, 2017

Date Posted: December 27, 2017

Recall Number: Z-0268-2018

Event ID: 78733

Reason for Recall:

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.

Status: Terminated

Product Quantity: 1079

Code Information:

SureSigns VSi : 863275, 863276, 863277 SureSigns VS2+ : 863278, 863279

Distribution Pattern:

Worldwide distribution. Australia, Austria, Bahrain, Belgium, Brazil, Denmark, France, French Polynesia, Germany, Hong Kong, India, Ireland, Israel, Italy, Kenya, Lebanon, Lesotho, Malaysia, Maldives, Morocco, Netherlands, Oman, Pakistan, Palestine, Poland, Saudi Arabia, South Africa, Spain, Sweden, Thailand, Turkey, United Kingdom, UAE, Vietnam, and Zimbabwe.

Voluntary or Mandated:

Voluntary: Firm initiated