Philips Medical Systems, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0022-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Philips Healthcare Integris Allura 15 -12 Fluoroscopy x ray system

Product Classification:

Class II

Date Initiated: August 8, 2014

Date Posted: October 15, 2014

Recall Number: Z-0022-2015

Event ID: 69197

Reason for Recall:

Philips had discovered through a field service testing where a device failed to comply with a Federal standard.

Status: Terminated

Product Quantity: one system

Code Information:

Model Number: Integris Allura 15-12 Serial Number: 16741023

Distribution Pattern:

US distribution to FL

Voluntary or Mandated:

Voluntary: Firm initiated