Philips recalls Allura CV20 patient tables with system code 722031 due to finger entrapment hazard during manual repositioning. Affected users should stop using until a fix is implemented.
Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
Philips is recalling Allura CV20 patient tables with system code 722031 because during manual repositioning, fingers can get trapped between the tabletop and guiding rails. This risk could cause finger injuries for operators and service personnel.
During manual repositioning of the patient tabletop, a finger can get stuck between the longitudinal guiding rails and the tabletop. This entrapment could cause finger injuries, particularly for people who handle the equipment regularly.
Operators and service personnel who use Philips Allura CV20 patient tables with system code 722031 are most at risk. The hazard applies to both tilt and non-tilt versions of the tables.
Check for the Allura CV20 system with code 722031. The product is sold under Philips Medical Systems Netherlands B.V. and may be used in medical facilities.
Do not use the Allura CV20 patient tables with system code 722031 until a fix is implemented.
The system code is 722031 for the Allura CV20 patient tables.
The recall record does not mention a fix or remedy.
Operators and service personnel who manually reposition the patient tabletops.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1076-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1076-2025 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.
