FDA Device recall Z-2340-2015
Siemens Artis zee systems
- FDA Device
- Class II
- terminated
- Published 2015-08-12
On 2015-08-12 the FDA classified a Class II recall of Siemens Artis zee systems by Siemens Medical Solutions Usa, citing the possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may n….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2340-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-29 |
| Published | 2015-08-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures.
Reason
The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported.
Identifiers
| code_info | Model Number of device: 10094141 10094143 10094137 10094135 10094142 10848280 10280959 10848283 10848353 ser…Model Number of device: 10094141 10094143 10094137 10094135 10094142 10848280 10280959 10848283 10848353 serial numbers: 146669 153131 153229 160851 146877 146996 146663 147100 124002 147049 147678 146406 146407 146411 136077 154502 135746 153172 153315 153317 153318 160879 146121 146710 137165 146945 147084 153992 147189 147190 153335 153695 135120 135322 146679 153101 153102 146232 147573 154616 153727 146408 146409 146728 146335 146659 153779 146993 137226 153280 153648 153674 160395 146898 153166 154536 146965 160484 135757 136513 135000 137103 146221 153700 154096 147273 154454 146814 146871 135914 146952 147030 147239 146988 153834 160348 147677 160502 160351 146899 153194 135102 147562 153169 154532 146643 136042 153803 160817 105007 147608 146650 136085 146980 146361 146365 146366 146369 146912 135927 147036 146116 146164 146168 153110 147581 147604 160392 1538 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2340-2015%22
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