FDA Device recall Z-0762-2024
Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, O…
- FDA Device
- Class II
- ongoing
- Published 2024-01-24
On 2024-01-24 the FDA classified a Class II recall of Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, O… by Getinge Usa Sales, citing A potential for a light system to fall in the operating room.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0762-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-11-08 |
| Published | 2024-01-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Getinge Usa Sales |
| Distribution | US |
Product
Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD QL AIR03 E - ARD568803967, OHDII FHD QL AIR04 E/U - ARD568803968, OHDII FHD QL+ VP01 - ARD569204944, OHDII AIR03 QL FHD E - ARD568803951
Reason
A potential for a light system to fall in the operating room.
Identifiers
| code_info | All systems affected UDI-DI: 3700712415761 3700712415976 3700712418274 3700712418281 3700712412340 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0762-2024%22
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