Sklar® 17-1262Recalls & reported problems
Sklar Corporation · RANKIN KELLY FCP STR 6.25" · Class 1
Data updated Oct 13, 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 10649111140532), received between Feb 3, 2026 and Feb 3, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 3, 2026Fracture
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FRACTURE WHICH LED TO THE REMOVAL OF THE IMPLANT.
Patient problems: Failure of Implant
MAUDE report 24246866 ↗
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- Sklar Instruments 96-2549Sklar Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Centurion I68420Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Centurion 66195Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion 66440Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion TRI66875Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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