FDA Device recall Z-2526-2018
Artis zee systems with Laird Cooling Unit for SSFD: Material # 7555118
- FDA Device
- Class II
- terminated
- Published 2018-08-01
On 2018-08-01 the FDA classified a Class II recall of Artis zee systems with Laird Cooling Unit for SSFD: Material # 7555118 by Siemens Medical Solutions Usa, citing due to a defective sealing, coolant may inflow into the electrical parts of the system cabinet, which could cause a short circuit and cause the system to shut down suddenly during….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2526-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-25 |
| Published | 2018-08-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | HI, IL, MI, NC, NY, VA, WI |
Product
Artis zee systems with Laird Cooling Unit for SSFD: Material # 7555118. Artis is an angiography system developed for single and biplane diagnostic imaging and interventional procedures.
Reason
Due to a defective sealing, coolant may inflow into the electrical parts of the system cabinet, which could cause a short circuit and cause the system to shut down suddenly during an ongoing procedure
Identifiers
| code_info | Laird Cooling Unit for SSFD: Material # 7555118. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2526-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.