Philips Medical Systems Nederlands: Medical Device Recall in 2019 - (Recall #: Z-0694-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Ingenia Elition S, Ingenia Elition X

Product Classification:

Class II

Date Initiated: December 3, 2018

Date Posted: January 16, 2019

Recall Number: Z-0694-2019

Event ID: 81797

Reason for Recall:

During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.

Status: Terminated

Product Quantity: 35

Code Information:

Software version R5.5.0 Serial numbers: 45027 45011 45010 45024 45032 45026 45054 45035 45051 45052 45007 45043 45044 45031 45039 45025 46001 45033 45050 45034 45049 45037 45048 46004 45046 45008 45058 45028 45029 45030 45042 46005 46011 45040 45045

Distribution Pattern:

CA, MN, NJ, NY, OH, TN, TX. Foreign distribution to Canada, Belgium, France, Germany, INdia, Japna, Netherlands, South Africa, Sweden, Switzerland, UAE.

Voluntary or Mandated:

Voluntary: Firm initiated