CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3813Recalls & reported problems
ALTATEC GmbH · CONELOG® PROGRESSIVE-LINE Implant, Promote® plus, d 3.8 mm, L 13 mm · Class 2 · Implant
All models of CONELOG PROGRESSIVE-LINE Implant, Promote plus (36)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 15
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI E219C108638131), received between Mar 7, 2024 and Oct 22, 2025 — classified as 15 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (9 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 Osseointegrate9
- Use of Device Problem6
- Connection Problem1
Patient problems
- Insufficient Information15
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
InjuryOct 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 16, 2025Connection Problem; Connection Problem
InjuryMay 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 8, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 2, 2025Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 21750686 ↗InjuryMar 4, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 23, 2025Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 21217118 ↗InjuryOct 29, 2024Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 20562172 ↗InjuryOct 11, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 25, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 9, 2024Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 19955214 ↗InjuryAug 9, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 8, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 19, 2024Use of Device Problem; Failure to Osseointegrate; Use of Device Problem; Failure to Osseointegrate
InjuryMar 7, 2024Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 18859557 ↗
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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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