FDA Device recall Z-2247-2024
First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer
- FDA Device
- Class II
- ongoing
- Published 2024-07-10
On 2024-07-10 the FDA classified a Class II recall of First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer by First Source, citing potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2247-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-09 |
| Published | 2024-07-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | First Source |
| Distribution | US |
Product
First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer.
Reason
Potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient.
Identifiers
| code_info | Model No. Pending; UDI-DI: G221500MC0740; Serial No. 4001, 4002, 4003, 4004, 4005, 4006, 4007, 4008, 4009, 4010, 4011,…Model No. Pending; UDI-DI: G221500MC0740; Serial No. 4001, 4002, 4003, 4004, 4005, 4006, 4007, 4008, 4009, 4010, 4011, 4012, 4013, 4014, 4015, 4016, 4017, 4018, 4019, 4020, 4021, 4022, 4023, 4024, 4025, 4026, 4027, 4028, 4029, 4030, 4031, 4032, 4033, 4034, 4035, 4036, 4037, 4038, 4039, 4040, 4041, 4042, 4043, 4044, 4045, 4046, 4047, 4048, 4049, 4050, 4051, 4052, 4053, 4054, 4055, 4056, 4057, 4058, 4059, 4060. |
|---|
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-2247-2024%22
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