FDA Device recall Z-2120-2015
GE Healthcare Precision 500D Classical R & F system
- FDA Device
- Class II
- terminated
- Published 2015-07-29
On 2015-07-29 the FDA classified a Class II recall of GE Healthcare Precision 500D Classical R & F system by Ge Healthcare, citing A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD moni….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2120-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-12 |
| Published | 2015-07-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Healthcare Precision 500D Classical R & F system.
Reason
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
Identifiers
| code_info | Mfg Lot or Serial # 00000002243MC4 00000017545MC9 00000001018MC1 00000001083MC5 00000003942MC0 00000001707MC9 00…Mfg Lot or Serial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|
|---|
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-2120-2015%22
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