Recall Z-0683-2016— Iba Dosimetry Gmbh

Name: FDA recall Z-0683-2016
Creator: U.S. Food and Drug Administration
Published: 2015-12-10

Class II · Terminated

Class II FDA medical device recall by Iba Dosimetry Gmbh, initiated 2015-12-10, terminated 2018-08-08. It names one FDA 510(k) clearance: K945321. Product: IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2. Reason: 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..

Recalling firm: Iba Dosimetry Gmbh
Classification: Class II
Status: Terminated
Initiated: 2015-12-10
Terminated: 2018-08-08
Firm location: Schwarzenbruck, N/A, Germany

510(k) clearances named in this recall

1 on FDA's record

K945321 — WELLHOFER WP700 V. 3.2Medical Physics Instrumentation, Inc.·cleared 1995-07-12

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

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

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.

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