Atlas FDA

IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2

FDA device recall Z-0683-2016 · posted 2016-01-21 · Terminated

Recall details

Recalling firm
Iba Dosimetry Gmbh
Reason for recall
When the electric lift table is connected to the mains power, in a very rare occasion, the table may start to move up in an uncontrolled manner.
Action taken
The field safety notice including a confirmation of receipt was sent to the affected hospitals; by email on 12/10/2015 then followed by 12/17/2015 sent by Fed Ex. The firm requested the mains power be disconnected after setting up the table and BP. Replacement part and instructions will follow.
Root cause
Component design/selection
Status
Terminated
Product code
IYE
Distribution
Nationwide and International: Algeria, Angola, Arab Republic of Egypt, Austria, Belarus, Belgium, Bulgaria, Bosnia and Herzegovina, Croatia, Czech Republic, Denmark, Ethiopia, France, Germany, Ghana,
Date initiated
2015-12-10
Date posted
2016-01-21
Date terminated
2018-08-08
Location
Schwarzenbruck, Germany

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.

Related 510(k) clearances

RecordFirmDate
WELLHOFER WP700 V. 3.2 (K945321)Medical Physics Instrumentation, Inc.1995-07-12