CONELOG® SCREW-LINE Implant, Promote® plus C1065.3309Recalls & reported problems
ALTATEC GmbH · CONELOG® SCREW-LINE Implant, Promote® plus, screw-mounted, d 3.3 mm, L 9 mm · Class 2 · Implant
All models of CONELOG SCREW-LINE Implant, Promote plus (44)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI E219C106533091), received between Apr 11, 2024 and Dec 2, 2025 — classified as 10 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (7 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.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate7
- Use of Device Problem4
Patient problems
- Insufficient Information10
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryDec 2, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 2, 2025Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 23693762 ↗InjuryDec 2, 2025Use of Device Problem; Failure to Osseointegrate; Use of Device Problem; Failure to Osseointegrate
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 23693619 ↗InjuryMay 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 11, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 9, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 21, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 10, 2024Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 19500348 ↗InjuryMay 8, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 19272329 ↗InjuryApr 11, 2024Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 19086642 ↗
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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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