# FDA recall Z-1690-2024

> **Philips North America Llc** · Class II · device recall initiated 2024-03-22.

## Product

Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS):  1.	APC (Schneider Electric IT Corporation) 120V Uninterruptable Power Supply  	Model: SCL500RM1U    2.	APC (Schneider Electric IT Corporation) 230V Uninterruptable Power Supply	        Model: SCL500RMI1U

## Reason for recall

Possible failure of Uninterruptable Power Supply (UPS) devices supporting the Patient Information Center (PIC) iX system, potential for the associated PIC iX system to shut down due to the lack of power.  may lead to the delay in the detection of a change in a patient condition

## Distribution

Worldwide distribution - US Nationwide and the countries of Argentina, Aruba, Australia,  Austria, Belgium, Bolivia, Canada, Chile, China, Colombia, Costa Rica, Czech Republic,  Ecuador, Estonia, Fiji, Finland, France, Germany, Greece, Hong Kong, India, Indonesia,  Iran, Ireland, Israel, Italy, Kazakhstan, Kenya, Kuwait, Latvia, Lebanon, Malaysia, Mexico,  Myanmar, Netherlands, New Zealand, Oman, Philippines, Poland, Portugal, Puerto Rico,  Qatar, Romania, Saudi Arabia, Singapore, South Africa, Spain, Switzerland, Taiwan,  United Kingdom, Utd. Ara Emir.

## Key facts

- **Recall number:** Z-1690-2024
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-22
- **Report date:** 2024-05-01

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1690-2024

## Citation

> AI Analytics. FDA recall Z-1690-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-1690-2024. Source: US FDA. Licensed CC0.

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