Z-2247-2024 Class II Ongoing
FDA device recall Z-2247-2024 was initiated by First Source Inc on May 9, 2024 and is designated Class II. Reason for recall: Potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient. The recall status is ongoing. Affected quantity: 137 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 10, 2024
- Initiation Date
- May 9, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 137 units
Product Description
First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer.
Reason for Recall
Potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient.
Distribution Pattern
Worldwide - US Nationwide distribution in the states of AR, CA, FL, GA, IL, IN, LA, MA, MD, MI, MO, MS, NC, NY, OK, PA, TN, TX, & VA. The countries of Korea & Serbia.
Code Information
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.