Philips North America Llc: Medical Device Recall in 2023 - (Recall #: Z-0272-2024)

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 4 Chest/Emergency, 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-0272-2024

Event ID: 93200

Reason for Recall:

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

Status: Ongoing

Product Quantity: 13 units

Code Information:

Model No. 712029 & 712033; UDI: (01)00884838074521(21) SN19000272, (01)00884838074521(21) SN19000213 , (01)00884838074521(21) 10001077, (01)00884838074521(21) SN20000097, (01)00884838074521(21) SN16000074, (01)00884838074521(21) SN15000238, (01)00884838074521(21) SN16000075, (01)00884838074521(21) SN15000367, (01)00884838074521(21) SN18000428, (01)00884838074521(21) SN17000318, (01)00884838074521(21) SN18000309, (01)00884838074521(21) SN18000204; Serial No. SN15000409, SN19000272, SN19000213, 10001077, SN20000097, SN16000074, SN15000238, SN16000075, SN15000367, SN18000428, SN17000318, SN18000309, SN18000204.

Distribution Pattern:

Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated