First Source Inc: Medical Device Recall in 2024 - (Recall #: Z-2247-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer.

Product Classification:

Class II

Date Initiated: May 9, 2024

Date Posted: July 10, 2024

Recall Number: Z-2247-2024

Event ID: 94744

Reason for Recall:

Potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient.

Status: Ongoing

Product Quantity: 137 units

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.

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.

Voluntary or Mandated:

Voluntary: Firm initiated