FDA Device recall Z-1973-2019
A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)
- FDA Device
- Class II
- terminated
- Published 2019-07-24
On 2019-07-24 the FDA classified a Class II recall of A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106) by Spinefrontier, citing there is a potential for the driver to bind up when attempting to advance the intervertebral body fixation screw.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1973-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-13 |
| Published | 2019-07-24 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Spinefrontier |
| Distribution | AZ, FL, MD, MO |
Product
A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)
Reason
There is a potential for the driver to bind up when attempting to advance the intervertebral body fixation screw.
Identifiers
| code_info | Lot EC20 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1973-2019%22
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