Philips Medical Systems Gmbh, DMC: Medical Device Recall in 2018 - (Recall #: Z-2844-2018)

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 (Stitching Patient Support) 712025

Product Classification:

Class II

Date Initiated: June 27, 2018

Date Posted: August 29, 2018

Recall Number: Z-2844-2018

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: 510694/SN12000240 510890/SN12000259 511451/SN13000066 510334/SN12000218 511346/SN13000008 511214/SN12000353 12000161 510089/SN12000293

Distribution Pattern:

US Nationwide; International to 66 countries

Voluntary or Mandated:

Voluntary: Firm initiated