PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Medical Device Recall in 2024 - (Recall #: Z-2716-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional Fluoroscopic X-Ray System, Model Numbers 722010, 722012, 722013

Product Classification:

Class II

Date Initiated: August 8, 2024

Date Posted: August 28, 2024

Recall Number: Z-2716-2024

Event ID: 95144

Reason for Recall:

A half-threaded bolt was included in the LTE kits instead of the correct full-threaded bolt.

Status: Ongoing

Product Quantity: 6 units

Code Information:

Serial Numbers: 111 138 467 817 2928 269

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of IL and OR. The countries of Hungary, Ireland, Poland, UK.

Voluntary or Mandated:

Voluntary: Firm initiated