Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera Connect R2.1 L 1 SP2 , incomplete...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Healthcare Inc. directly.
Affected Products
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.
Quantity: 226 units
Why Was This Recalled?
Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from unformatted reports interface
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Healthcare Inc.
Philips Healthcare Inc. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report