HTR-PEKK PK618278Recalls & reported problems
Oxford Performance Materials, Inc. · Class 2 · Implant
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 00813298024012), received between Jan 16, 2017 and Jan 17, 2017.
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
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Unspecified Infection2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
Jan 17, 2017Adverse Event Without Identified Device or Use Problem
THE IMPLANT WAS REMOVED DUE TO AN INFECTION. THE CAUSE OR THE SOURCE OF THE INFECTION ARE UNKNOWN. THE IMPLANT IS SHIPPED NON-STERILE AND THEN STERILIZED AT THE HEALTHCARE FACILITY ACCORDING TO THE INSTRUCTIONS FOR USE. THERE ARE NO STERILIZATION, PATHOLOGY, OR SURGICAL RECORDS AVAILABLE.
Patient problems: Unspecified Infection
MAUDE report 6255603 ↗Jan 16, 2017Adverse Event Without Identified Device or Use Problem
THE IMPLANT WAS REMOVED DUE TO AN INFECTION. THE CAUSE OR THE SOURCE OF THE INFECTION ARE UNKNOWN. THE IMPLANT IS SHIPPED NON-STERILE AND THEN STERILIZED AT THE HEALTHCARE FACILITY ACCORDING TO THE INSTRUCTIONS FOR USE. THERE ARE NO STERILIZATION, PATHOLOGY, OR SURGICAL RECORDS AVAILABLE.
Patient problems: Unspecified Infection
MAUDE report 6254490 ↗
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- NA SD800.433Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE8 reports
- IPS 60-000-23-09KLS-Martin L.P. · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE7 reports
- NA SD800.540Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE6 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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