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Recall

Class II — Iba Dosimetry Gmbh

Recalling firmIBA Dosimetry GmbH
Registered facilityView this company's 2 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonWhen 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.
ProductIBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2
QuantityN/A
DistributionNationwide 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 Arabia, Kuwait, Lebanon, Libya, Morocco
Initiated2015-12-10
Classified2016-01-21
Terminated2018-08-08
Recall numberZ-0683-2016
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Iba Dosimetry Gmbh (Z-0683-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73036/

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