# FDA recall Z-0072-2022

> **Innovative Orthopedic Technologies, LLC** · Class II · device recall initiated 2021-09-13.

## Product

ARCH Leg Positioning System

## Reason for recall

Due to the holes not being bored to the specific diameter, the locking pins are unable to engage under a load.

## Distribution

U.S. Nationwide distribution in the states of AL, AZ, FL, MI, MN, OK, SD, and TX.

## Key facts

- **Recall number:** Z-0072-2022
- **Recalling firm:** Innovative Orthopedic Technologies, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-09-13
- **Report date:** 2021-10-13
- **Termination date:** 2024-01-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Winnie, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0072-2022

## Citation

> AI Analytics. FDA recall Z-0072-2022. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0072-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
