CONCORDE LIFT 1978-11-027LRecalls & reported problems
Medos International Sàrl · CONCORDE LIFT EXPANDABLE INTERBODY DEVICE LORDOTIC CAGE 11X27 mm · Class 2 · Implant
All models of CONCORDE LIFT (13)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034531588), received between Aug 6, 2019 and Aug 6, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K171425); 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Migration1
Patient problems
- No Code Available1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 6, 2019Migration; Migration
IT WAS REPORTED THAT ON (B)(6) 2019, THE CONCORDE LIFT CAGE IMPLANT WAS REMOVED, ORIGINALLY THE PATIENT HAD A TRANSFORAMINAL LUMBAR INTERBODY FUSION (TLIF) SURGERY ON (B)(6) 2019, THE CONCORDE LIFT CAGE IMPLANT WAS REMOVED SINCE THE PATIENT EXPERIENCED PAIN DUE TO CAGE MOVEMENT. IT WAS REPLACED WITH TPAL PROTI. THE PROCEDURE OUTCOME WAS UNKNOWN. THERE WAS PATIENT CONSEQUENCE. THIS COMPLAINT INVOLVES ONE (1) DEVICE.
Patient problems: No Code Available; Pain
MAUDE report 8864676 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K171425. One submission often covers many models, so check the product and lot details in each record.
- Z-1225-2019 · Apr 8, 2019 · TerminatedConcorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (197811026C), 9x21 (US197809021C), 9x26 (U
- Z-0848-2018 · Jul 26, 2017 · TerminatedConcorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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