FDA Device recall Z-0522-2019
Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients
- FDA Device
- Class II
- ongoing
- Published 2018-12-05
On 2018-12-05 the FDA classified a Class II recall of Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients by Ge Healthcare, citing the patient monitors may simultaneously restart as designed if all are connected to the same network and a network overload occurs for a prolonged time.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0522-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-08-31 |
| Published | 2018-12-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
Reason
The patient monitors may simultaneously restart as designed if all are connected to the same network and a network overload occurs for a prolonged time.
Identifiers
| code_info | All monitors |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0522-2019%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.