Philips North America Llc: Medical Device Recall in 2023 - (Recall #: Z-0278-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images.

Product Classification:

Class II

Date Initiated: September 21, 2023

Date Posted: November 15, 2023

Recall Number: Z-0278-2024

Event ID: 93200

Reason for Recall:

Potential for units suspended on the ceiling to fail and fall.

Status: Ongoing

Product Quantity: 2 units

Code Information:

Model No. 712026; Serial No. SN14000197 & SN14000260.

Distribution Pattern:

Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated