Recall Z-2194-2017— GE Healthcare, LLC

Name: FDA recall Z-2194-2017
Creator: U.S. Food and Drug Administration
Published: 2017-05-19

Class II · Terminated

Class II FDA medical device recall by GE Healthcare, LLC, initiated 2017-05-19, terminated 2018-07-29. It names one FDA 510(k) clearance: K093514. Product: GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system. Reason: It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed..

Recalling firm: GE Healthcare, LLC
Classification: Class II
Status: Terminated
Initiated: 2017-05-19
Terminated: 2018-07-29
Firm location: Waukesha, WI, United States

510(k) clearances named in this recall

1 on FDA's record

K093514 — DISCOVERY MODEL NM/CT 670Ge Medical Systems F.I. Haifa·cleared 2009-12-10

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system

Reason for recall

It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.

Data sourced from openFDA. This site is unofficial and independent of the FDA.