Philips Medical Systems Gmbh, DMC: Medical Device Recall in 2018 - (Recall #: Z-2845-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026

Product Classification:

Class II

Date Initiated: June 27, 2018

Date Posted: August 29, 2018

Recall Number: Z-2845-2018

Event ID: 80577

Reason for Recall:

The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.

Status: Terminated

Product Quantity:

Code Information:

Serial Numbers: SN13000495 SN14000058 SN13000463 SN14000051 SN14000214 SN14000047 SN14000077 SN13000484 SN14000082 SN14000163 SN14000133 SN14000134 SN14000134 SN14000023 SN14000041

Distribution Pattern:

US Nationwide; International to 66 countries

Voluntary or Mandated:

Voluntary: Firm initiated