BioHorizons PXMUTCRecalls & reported problems
Biohorizons Implant Systems, Inc · Titanium Coping, Multi-unit · Class 1 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00847236006686), received between Jul 31, 2025 and Apr 9, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Compatibility Problem” (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
- Compatibility Problem1
- Fitting Problem1
- Manufacturing, Packaging or Shipping Problem1
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 9, 2026Manufacturing, Packaging or Shipping Problem
THERE WAS NO PRODUCT IN THE PACKAGE.
Patient problems: Insufficient Information
MAUDE report 24830622 ↗MalfunctionJul 31, 2025Fitting Problem; Compatibility Problem; Fitting Problem; Compatibility Problem
THIS REPORT INDICATES ONE (1) MALFUNCTION EVENT. A REVIEW OF THE EVENT INVOLVED THE DEVICE HAVING A SEATING ISSUE . NO PATIENT ADVERSE EVENT WAS REPORTED. NO INFORMATION REGARDING PATIENT DEMOGRAPHICS WERE PROVIDED.
Patient problems: Insufficient Information
MAUDE report 22682580 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.