Philips Healthcare Inc.: Medical Device Recall in 2012 - (Recall #: Z-1942-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: June 14, 2012

Date Posted: July 11, 2012

Recall Number: Z-1942-2012

Event ID: 62270

Reason for Recall:

Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from unformatted reports interface

Status: Terminated

Product Quantity: 226 units

Code Information:

Software R2.1 L 1 SP2

Distribution Pattern:

Worldwide Distribution-USA (nationwide) and the countries of Argentina, Chile, Denmark , Estonia, Finland, France, Germany ,Hong Kong, Ireland, Italy, Malaysia, Netherlands, Poland, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Taiwan, United Kingdom, and Utd. Arab. Emir.

Voluntary or Mandated:

Voluntary: Firm initiated