Icotec Ag recalls
Icotec Ag appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2024-01-17.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 3 |
|---|---|
| Published | 2022-12-28 to 2024-01-17 |
| By agency | FDA Device (3) |
| By classification | Class II (3) |
| By status | ongoing (3) |
| Distribution named in notices | AZ, CA, CO, DE, MI, NC, NY, OH, PA, TX, US |
Recalls
- VADER pedicle system, torque wrench, Catalog Number 42-703
FDA Device · Class II · 2024-01-17 · Icotec Ag
Reason: icotec has received notification of one revision that had to be carried out because nut screws had become loose. During the investigation of the device involved, it was detected that the torque limiting function of the… - VADER pedicle system, torque wrench, Catalog Number 42-702
FDA Device · Class II · 2024-01-17 · Icotec Ag
Reason: icotec has received notification of one revision that had to be carried out because nut screws had become loose. During the investigation of the device involved, it was detected that the torque limiting function of the… - VADER Pedicle System Torque Wrench, Hudson Coupling, 12 Nm, REF 42-702
FDA Device · Class II · 2022-12-28 · Icotec Ag
Reason: During internal testing (at manufacturer site) of two torque wrench devices, it was detected that the torque limiting function was out of specification. The specified torque limiting value is 12 Nm. The measuring result…