PlainRecalls
FDA Devices Moderate Class II Terminated

Ingenia Elition S, Ingenia Elition X

Reported: January 16, 2019 Initiated: December 3, 2018 #Z-0694-2019

Product Description

Ingenia Elition S, Ingenia Elition X

Reason for Recall

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

Details

Units Affected
35
Distribution
CA, MN, NJ, NY, OH, TN, TX. Foreign distribution to Canada, Belgium, France, Germany, INdia, Japna, Netherlands, South Africa, Sweden, Switzerland, UAE.
Location
Best

Frequently Asked Questions

What product was recalled?
Ingenia Elition S, Ingenia Elition X. Recalled by Philips Medical Systems Nederlands. Units affected: 35.
Why was this product recalled?
During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 16, 2019. Severity: Moderate. Recall number: Z-0694-2019.