CONDUIT LLIF Squid Inserter LET30290TRecalls & reported problems
Enztec Limited · Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 09421028116459), received between Jun 7, 2023 and Jun 7, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Positioning” (2 reports).
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
- Difficult or Delayed Positioning2
Patient problems
- Hemorrhage/Blood Loss/Bleeding2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 7, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning
DURING USE OF THE INSTRUMENT, THE IMPLANT ROTATED UNEXPECTEDLY ANTERIORLY IN THE DISC SPACE SUCH THAT THE IMPLANT HAD TO BE RE-INSERTED DURING THE SAME PROCEDURE. THERE WAS NO DAMAGE TO THE IMPLANT OR INSTRUMENT REPORTED, AND THE DEVICE MECHANISM DOES NOT APPEAR TO HAVE MALFUNCTIONED. THERE WERE NO POST-OPERATIVE COMPLICATIONS REPORTED. INCIDENT OCCURRED IN SWITZERLAND.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 17077030 ↗MalfunctionJun 7, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning
DURING USE OF THE INSTRUMENT, THE IMPLANT ROTATED UNEXPECTEDLY ANTERIORLY IN THE DISC SPACE SUCH THAT THE IMPLANT HAD TO BE RE-INSERTED DURING THE SAME PROCEDURE. THERE WAS NO DAMAGE TO THE IMPLANT OR INSTRUMENT REPORTED, AND THE DEVICE MECHANISM DOES NOT APPEAR TO HAVE MALFUNCTIONED. THERE WERE NO POST-OPERATIVE COMPLICATIONS REPORTED. INCIDENT OCCURRED IN SWITZERLAND.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 17077012 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page