Philips recalls Zenition 50 and 70 Mobile Surgery C-arms delivered to Puerto Rico without warning labels and missing Source-to-Skin Distance Spacer. Affected units may pose safety risks.
Philips has become aware of an issue with the Philips Integris-Allura, Allura Xper and Azurion systems that have been delivered to Puerto Rico without a warning label and the Source-to-Skin Distance Spacer (Tube-spacer) is missing.
Philips is recalling Zenition 50 and 70 Mobile Surgery C-arms that were delivered to Puerto Rico without warning labels and missing a critical spacer component. This could lead to safety issues during medical procedures.
The missing Source-to-Skin Distance Spacer (Tube-spacer) could cause improper positioning during surgery, potentially leading to safety risks. Devices delivered to Puerto Rico without warning labels may not meet safety standards.
Medical facilities in Puerto Rico that received these specific Zenition 50 and 70 Mobile Surgery C-arms are likely affected. Healthcare providers using these devices for surgery may be at risk.
Check for Zenition 50 models with serial numbers 974, 1244, 1247, or 892 and Zenition 70 models with serial numbers 1735 or 1824. These units were delivered to Puerto Rico without warning labels.
Verify the model and serial number to confirm if your device is in the recall list.
Philips has become aware that some Zenition 50 and 70 Mobile Surgery C-arms delivered to Puerto Rico lack warning labels and have a missing Source-to-Skin Distance Spacer.
The recall record does not specify a remedy, so contact Philips directly for guidance.
Yes, Zenition 50 models with serial numbers 974, 1244, 1247, or 892 and Zenition 70 models with serial numbers 1735 or 1824 were delivered to Puerto Rico without warning labels.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0226-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0226-2024 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
