Iba Dosimetry Gmbh recalls IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2
- Recall date
- December 10, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0683-2016
- FDA classification
- Class II
- Brand / firm
- Iba Dosimetry Gmbh
- Sold / distributed
- Nationwide and International: Algeria, Angola, Arab Republic of Egypt, Austria, Belarus, Belgium, Bulgaria, Bosnia and Herzegovina, Croatia, Czech Republic, Denmark, Ethiopia, France, Germany, Ghana, Greece, Hungary, Iraq, Ireland, Islamic Republic Iran, Italy, Kazakhstan, Kenya, Kingdom of Saudi A…
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2
Get recall alerts
Free email alert whenever Iba Dosimetry Gmbh has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Iba Dosimetry Gmbh