ARCH Leg Positioning System — Class II medical device recall Z-0072-2022
Terminated recall by Innovative Orthopedic Technologies, LLC, reported 2021-10-13, distributed nationwide. Due to the holes not being bored to the specific diameter, the locking pins are unable to engage under a load.
| Recall number | Z-0072-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Innovative Orthopedic Technologies, LLC, Winnie, TX, United States |
| Recall initiated | 2021-09-13 |
| Classified | 2021-10-07 |
| Reported by FDA | 2021-10-13 |
| Terminated | 2024-01-29 |
| Distributed | Nationwide (US) |
| Quantity | 10 units |
| Serial numbers | 6813010.0066, 6813010.0067, 6813010.0069, 6813010.0070, 6813010.0071, 6813010.0072, 6813010.0073, 6813010.0074, 6813010.0075, 6813010.0076 |
| Model numbers | 6813010 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0072-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.