Tyber Medical, LLC
92 devices · 101 adverse event reports · 1 deaths reported · 20 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- A.L.P.S. mvX™ 770708042Plate, fixation, bone1 recall1 report
- A.L.P.S. mvX™ 770708041Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708061Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708062Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708081Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708082Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708101Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708102Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708121Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770708122Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715061Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715062Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715101Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715102Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715121Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715122Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715161Plate, fixation, bone1 recall0 reports
- A.L.P.S. mvX™ 770715162Plate, fixation, bone1 recall0 reports
- VOLT™ Wrist Treatment System 02.426.681SPlate, fixation, bone1 recall0 reports
- VOLT™ Wrist Treatment System 02.426.691SPlate, fixation, bone1 recall0 reports
- T-PAL™ ProTi 360°™ 108812007Intervertebral fusion device with bone graft, lumbar5 reports
- Cannulated Screw System + 04.355.895Screw, fixation, bone4 reports
- T-PAL™ ProTi 360°™ 108812009Intervertebral fusion device with bone graft, lumbar4 reports
- T-PAL™ ProTi 360°™ 108812010Intervertebral fusion device with bone graft, lumbar4 reports
- CONCORDE® ProTi 360°™ 188827107Intervertebral fusion device with bone graft, lumbar3 reports
- T-PAL™ ProTi 360°™ 108812008Intervertebral fusion device with bone graft, lumbar3 reports
- Cannulated Compression Headless Screw 04.333.124TSScrew, fixation, bone3 reports
- ACIS® ProTi 360°™ 108843306Intervertebral fusion device with bone graft, cervical2 reports
- CONCORDE® ProTi 360°™ 188823107Intervertebral fusion device with bone graft, lumbar2 reports
- CONCORDE® ProTi 360°™ 188827408Intervertebral fusion device with bone graft, lumbar2 reports
- T-PAL™ ProTi 360°™ 108812208Intervertebral fusion device with bone graft, lumbar2 reports
- Cannulated Compression Headless Screw 04.334.240Screw, fixation, bone2 reports
- Cannulated Compression Headless Screw 04.334.440Screw, fixation, bone2 reports
- Cannulated Compression Headless Screw 04.333.765Screw, fixation, bone2 reports
- Cannulated Compression Headless Screw 04.333.226TSScrew, fixation, bone2 reports
- FuseFix Hammertoe M13-S20113-SScrew, fixation, bone2 reports
- UNITUS 15ZB00106Staple, fixation, bone1 report
- UNITUS 15ZB00111Staple, fixation, bone1 report
- UNITUS 15ZB00117Staple, fixation, bone1 report
- A.L.P.S. mvX™ 770150009Screw, fixation, bone1 report
- A.L.P.S. mvX™ 770150010Screw, fixation, bone1 report
- A.L.P.S. mvX™ 770300050Screw, fixation, bone1 report
- A.L.P.S. mvX™ 770002182BIT, DRILL1 report
- A.L.P.S. mvX™ 770240026Screw, fixation, bone1 report
- A.L.P.S. mvX™ 770714101Plate, fixation, bone1 report
- A.L.P.S. mvX™ 770714102Plate, fixation, bone1 report
- Volt™ Wrist Treatment System 02.426.530Plate, fixation, bone1 report
- Cannulated Screw System + 04.353.126Screw, fixation, bone1 death1 report
- Cannulated Screw System + 04.354.342Screw, fixation, bone1 report
- Cannulated Screw System + 04.354.350Screw, fixation, bone1 report
- Cannulated Screw System + 04.354.548Screw, fixation, bone1 report
- Cannulated Screw System + 04.353.660Screw, fixation, bone1 report
- Cannulated Screw System + 04.354.648Screw, fixation, bone1 report
- Cannulated Screw System + 04.355.885Screw, fixation, bone1 report
- Cannulated Screw System + 04.353.906.05Screw, fixation, bone1 report
- Cannulated Screw System + 04.353.655Screw, fixation, bone1 report
- ACIS® ProTi 360°™ 108843008Intervertebral fusion device with bone graft, cervical1 report
- ACIS® ProTi 360°™ 108843305Intervertebral fusion device with bone graft, cervical1 report
- ACIS® ProTi 360°™ 108843505Intervertebral fusion device with bone graft, cervical1 report
- ACIS® ProTi 360°™ 108843606Intervertebral fusion device with bone graft, cervical1 report
- CONCORDE® ProTi 360°™ 188823110Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188823111Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188823408Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188823409Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188823410Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188827409Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188827410Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188827411Intervertebral fusion device with bone graft, lumbar1 report
- CONCORDE® ProTi 360°™ 188827412Intervertebral fusion device with bone graft, lumbar1 report
- T-PAL™ ProTi 360°™ 108812011Intervertebral fusion device with bone graft, lumbar1 report
- T-PAL™ ProTi 360°™ 108812207Intervertebral fusion device with bone graft, lumbar1 report
- T-PAL™ ProTi 360°™ 108812209Intervertebral fusion device with bone graft, lumbar1 report
- T-PAL™ ProTi 360°™ 108812210Intervertebral fusion device with bone graft, lumbar1 report
- T-PAL™ ProTi 360°™ 108812216Intervertebral fusion device with bone graft, lumbar1 report
- ACIS® ProTi 360™ HL 208843005Intervertebral fusion device with bone graft, cervical1 report
- Cannulated Compression Headless Screw 04.334.028Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.334.444Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.333.530Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.334.502Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.333.642Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.333.650Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.334.655Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.334.660Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.333.750Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 04.334.750Screw, fixation, bone1 report
- Cannulated Compression Headless Screw 03.333.101ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Cannulated Compression Headless Screw 03.333.300Orthopedic manual surgical instrument1 report
- Cannulated Compression Headless Screw 03.333.302Orthopedic manual surgical instrument1 report
- Cannulated Compression Headless Screw 04.334.026TSScrew, fixation, bone1 report
- Cannulated Compression Headless Screw 04.333.224TSScrew, fixation, bone1 report
- Cannulated Compression Headless Screw 04.334.454TSScrew, fixation, bone1 report
- TPLIF Interbody System M2-P2410410-SIntervertebral fusion device with bone graft, cervical1 report