The Recall Desk
HighFDA (Devices)·Z-1076-2025·Announced 2025-02-12

Philips Allura CV20 patient tables risk finger entrapment during repositioning

The Philips Allura CV20 System patient tables (AD7 and AD7X models) pose a finger entrapment hazard during manual repositioning. Fingers can become caught between the tabletop and guiding rails, potentially injuring operators and service personnel.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: FDA Class II medical device with a documented risk of finger entrapment during normal operation. No injuries or hospitalizations are reported in the source material. This qualifies as a risk-of-harm product where injury has not yet been reported, meeting the rubric criterion for High severity.

Plain-English summary

Philips Medical Systems Nederland B.V. is recalling the Allura CV20 System, specifically the AD7 and AD7X patient tables in both tilt and non-tilt versions. These systems have been distributed worldwide, including throughout the United States, Canada, and numerous other countries.

During manual repositioning of the patient tabletop, a finger can become entrapped between the longitudinal guiding rails and the tabletop. This entrapment may result in finger injury. The hazard affects operators and service personnel who manually reposition these tables.

The recalled product

Product
Allura CV20 System Code: 722031
Manufacturer
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Category
Medical Device — Patient Positioning Table
Hazard
  • finger-entrapment
  • crush-injury

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • UDI: N/A

Distribution

Distributed nationwide across the United States.

Related recalls

Same category