FDA Device recall Z-1942-2012
Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange
- FDA Device
- Class II
- terminated
- Published 2012-07-11
On 2012-07-11 the FDA classified a Class II recall of Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange by Philips Healthcare, citing xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from unformatted reports interface.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1942-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-14 |
| Published | 2012-07-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Healthcare |
| Distribution | US |
Product
Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange. Philips Xcelera Connect R2.x is a generic interface and data mapping engine between a Hospital Information System (HIS), Imaging Modalities, Xcelera PACS and Xcelera Cath Lab Manager (CLM). This interface engine simplifies the connection by serving as a central point for data exchange. The data consists only of demographic patient information, schedules, textual information and text reports.
Reason
Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from unformatted reports interface
Identifiers
| code_info | Software R2.1 L 1 SP2 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1942-2012%22
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