FDA Device recall Z-0072-2022
ARCH Leg Positioning System
- FDA Device
- Class II
- terminated
- Published 2021-10-13
On 2021-10-13 the FDA classified a Class II recall of ARCH Leg Positioning System by Innovative Orthopedic Technologies, citing due to the holes not being bored to the specific diameter, the locking pins are unable to engage under a load.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0072-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-09-13 |
| Published | 2021-10-13 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Innovative Orthopedic Technologies |
| Distribution | US |
Product
ARCH Leg Positioning System
Reason
Due to the holes not being bored to the specific diameter, the locking pins are unable to engage under a load.
Identifiers
| code_info | Model: 6813010 Serial Numbers: 6813010.0066; 6813010.0067; 6813010.0069; 6813010.0070; 6813010.0071; 6813010.0072; 6813…Model: 6813010 Serial Numbers: 6813010.0066; 6813010.0067; 6813010.0069; 6813010.0070; 6813010.0071; 6813010.0072; 6813010.0073; 6813010.0074; 6813010.0075; 6813010.0076; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0072-2022%22
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