Cannulated 1st MPJ Hemi Implant CHI-2CHRecalls & reported problems
Vilex LLC · Cannulated Hemi Implant #2 17x15 CoCr HA Coated · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841731106179), received between Feb 27, 2018 and Feb 27, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 27, 2018Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
RECEIVED CALL ON (B)(6) 2018 FROM ACCOUNT MANAGER THAT SURGEON HAD AN ISSUE REMOVING THE GUIDEWIRE FROM THE IMPLANT ONCE IT WAS PARTIALLY IMPLANTED.
Patient problems: No Information
MAUDE report 7301590 ↗
Other Prosthesis, Toe, Hemi-, Phalangeal devices
- TOE JOINT TITANIUM NPC LG 23MM 16816Biopro, Inc. · Prosthesis, Toe, Hemi-, Phalangeal1 recall0 reports
- TOE JOINT TITANIUM NPC M/L 21.5MM 16815Biopro, Inc. · Prosthesis, Toe, Hemi-, Phalangeal1 recall0 reports
- TOE JOINT TITANIUM NPC MD 20MM 16814Biopro, Inc. · Prosthesis, Toe, Hemi-, Phalangeal1 recall0 reports
- TOE JOINT TITANIUM PC MD 20MM 17036Biopro, Inc. · Prosthesis, Toe, Hemi-, Phalangeal1 recall0 reports
- TOE JOINT TITANIUM NPC SM 17MM 16813Biopro, Inc. · Prosthesis, Toe, Hemi-, Phalangeal1 recall0 reports
- TOE JOINT TITANIUM PC M/S 18.5MM 17197Biopro, Inc. · Prosthesis, Toe, Hemi-, Phalangeal1 recall0 reports
- TOE JOINT TITANIUM PC SM 17MM 17035Biopro, Inc. · Prosthesis, Toe, Hemi-, Phalangeal1 recall0 reports
- BioPoly® Great Toe Hemiarthroplasty Implant 135-5118Biopoly, LLC · Prosthesis, Toe, Hemi-, Phalangeal3 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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