# FDA recall Z-2247-2024

> **First Source Inc** · Class II · device recall initiated 2024-05-09.

## Product

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

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.

## Key facts

- **Recall number:** Z-2247-2024
- **Recalling firm:** First Source Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-09
- **Report date:** 2024-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rochester, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2247-2024

## Citation

> AI Analytics. FDA recall Z-2247-2024. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2247-2024. Source: US FDA. Licensed CC0.

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