ALTERA 1124.1215Recalls & reported problems
Globus Medical, Inc. · ALTERA Spacer, 10 x 36, 12-16mm, 8° · Class 2 · Implant
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
21 other recalls cover devices cleared under the same FDA submission (K140411); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jul 22, 2020Terminated
Specific lots of ALTERA implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy.
Z-2868-2020 · Root cause: Nonconforming Material/Component · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K140411. One submission often covers many models, so check the product and lot details in each record.
- Z-2856-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x26, 10-14mm, 15
- Z-2858-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x31, 8-12mm, 8
- Z-2854-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x26, 12-16mm, 8
- Z-2865-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x36, 8-12mm, 8
- Z-2859-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x31, 9-13mm, 8
- Z-2870-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x36, 10-14mm, 15
- Z-2869-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x36, 9-13mm, 15
- Z-2867-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x36, 10-14mm, 8
- Z-2864-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x31, 12-16mm, 15
- Z-2855-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x26, 9-13mm, 15
- Z-2860-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x31, 10-14mm, 8
- Z-2863-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x31, 10-14mm, 15
- Z-2857-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x26, 12-16mm, 15
- Z-2853-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x26, 10-14mm, 8
- Z-2851-2020 · Jul 22, 2020 · TerminatedALTERA Spacer ALTERA Spacer, 10x26, 8-12mm, 8
…and 6 more.
Other Intervertebral fusion device with bone graft, lumbar devices
- T-PAL 03.812.003Synthes GmbH · Intervertebral fusion device with bone graft, lumbar152 reports
- T-PAL 03.812.004Synthes GmbH · Intervertebral fusion device with bone graft, lumbar120 reports
- Catalyft PL Expandable Interbody System 6068073Medtronic Sofamor Danek, Inc. · Intervertebral fusion device with bone graft, lumbar1 recall66 reports
- Catalyft PL Expandable Interbody System 6069076Medtronic Sofamor Danek, Inc. · Intervertebral fusion device with bone graft, lumbar1 recall51 reports
- Catalyft PL Expandable Interbody System 6068076Medtronic Sofamor Danek, Inc. · Intervertebral fusion device with bone graft, lumbar1 recall46 reports
- EIT TLIF Inserter TFT30101EIT Emerging Implant Technologies GmbH · Intervertebral Fusion Device With Bone Graft, Lumbar88 reports
- T-PAL 03.812.001Synthes GmbH · Intervertebral fusion device with bone graft, lumbar76 reports
- Catalyft PL Expandable Interbody System 6069096Medtronic Sofamor Danek, Inc. · Intervertebral fusion device with bone graft, lumbar1 recall25 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.