# FDA recall Z-0268-2018

> **Philips Electronics North  America Corporation** · Class III · device recall initiated 2017-09-20.

## Product

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

## 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.

## Distribution

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.

## Key facts

- **Recall number:** Z-0268-2018
- **Recalling firm:** Philips Electronics North  America Corporation
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-20
- **Report date:** 2017-12-27
- **Termination date:** 2020-04-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Andover, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0268-2018

## Citation

> AI Analytics. FDA recall Z-0268-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0268-2018. Source: US FDA. Licensed CC0.

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