Philips North America Llc: Medical Device Recall in 2025 - (Recall #: Z-1554-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.

Product Classification:

Class II

Date Initiated: March 10, 2025

Date Posted: April 23, 2025

Recall Number: Z-1554-2025

Event ID: 96435

Reason for Recall:

Potential for collimator to fall as a result of incorrect installation.

Status: Ongoing

Product Quantity: 83 units

Code Information:

REF 712214; UDI: (01)00884838064751(21); Serial No. SN170009, SN170010, SN180072, SN180020 200037, SN160061, SN180075, 200089, SN180045, SN160096.

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH, NY, OR, PA, TX, WI and the countries of Argentina, Australia, Canada, Chile, China, Germany, Hungary, India, Indonesia, Italy, Kenya, Mexico, Netherlands, New Zealand, Oman, Pakistan, Peru, Poland, Romania, Russian Federation, Slovenia, South Africa, Spain, Thailand, United Kingdom, Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated