Philips Medical Systems Gmbh, DMC: Medical Device Recall in 2018 - (Recall #: Z-2863-2018)

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 Single Detector (Stitching Patient Support) 712020

Product Classification:

Class II

Date Initiated: June 27, 2018

Date Posted: August 29, 2018

Recall Number: Z-2863-2018

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: 399921/SN08000023 410038/SN08000091 402577/SN09000137 479651/SN11000391 443237/SN09000411 496881/SN12000104 489345/SN11000590 459498/SN10000231 483525/SN11000377 468302/SN10000537 485692/SN11000443 422533/SN09000072 450553/SN10000089 414087/SN08000100 472611/SN11000056 443235/SN09000450 481036/SN11000471 471070/SN10000695 471047/SN10000700 455221/SN10000251 460072/SN10000336 478109/SN11000327 475856/SN11000315 415754/SN08000063 443660/SN10000010 440700/SN10000030 440260/SN09000350 447603/SN09000468 448647/SN10000111 467487/SN11000085 467484/SN10000602 477526/SN11000311 490997/SN12000106 451267/SN10000104 445433/SN09000434 488711/SN11000615 470906/SN11000142 485620/SN12000002 448671/SN10000076 480052/SN11000286 480053/SN11000288 439920/SN09000329 412942/SN08000036 418438/SN08000110 431111/SN09000237

Distribution Pattern:

US Nationwide; International to 66 countries

Voluntary or Mandated:

Voluntary: Firm initiated