IBA Dosimetry GmbH Lift Table Type 4320 — Class II medical device recall Z-0683-2016
Terminated recall by Iba Dosimetry Gmbh, reported 2016-01-27, distributed nationwide. When the electric lift table is connected to the mains power, in a very rare occasion, the table may start to
| Recall number | Z-0683-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Iba Dosimetry Gmbh, Schwarzenbruck, N/A, Germany |
| Recall initiated | 2015-12-10 |
| Classified | 2016-01-21 |
| Reported by FDA | 2016-01-27 |
| Terminated | 2018-08-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, BG, CZ, DE, DK, DZ, EG, FR, GH, GR, HR, HU, IE, IQ, IR, IT, KE, KW, LB, MA, SA |
| Serial numbers | 10158, 10159, 10160, 10184, 10185, 10186, 10187, 10236, 10237, 10238, 10239, 10240, 10241, 10242, 10243, 10244, 10245, 10286, 10287, 10288, 10289, 10304, 10306, 10307, 10308 and 432 more |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0683-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.