Philips Medical Systems Gmbh, DMC: Medical Device Recall in 2018 - (Recall #: Z-2868-2018)

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:

EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050

Product Classification:

Class II

Date Initiated: June 27, 2018

Date Posted: August 29, 2018

Recall Number: Z-2868-2018

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: SN17000027 SN16000011 SN16000014 SN16000036 SN16000015 SN15000050 476034/SN12000027 476338/SN12000026 SN17000022 SN15000029 SN16000017 SN16000009 SN13000078 SN16000048 SN16000004 SN13000029 SN14000068 511923/SN12000044 514827/SN12000098 514827/SN12000098 SN14000044 ***Updated 5/6/21*** SN15000055

Distribution Pattern:

US Nationwide; International to 66 countries

Voluntary or Mandated:

Voluntary: Firm initiated