TOUCH® CMC 1 NTO06Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07640181160013), received between Apr 17, 2026 and Sep 28, 2026 — classified as 5 injuries.

The most frequently reported specific device problem is “Break” (4 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 16, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjurySep 28, 2026Insufficient Device Problem Information

  Patient problems: Failure of Implant

  MAUDE report 50923023 ↗
• InjurySep 11, 2026Break

  It was reported that a patient underwent a total joint arthroplasty with a Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery due to PE liner breakage. No damage or impingement on cup was reported.

  Patient problems: Insufficient Information

  MAUDE report 50725367 ↗
• InjurySep 11, 2026Break

  It was reported that a patient underwent a total joint arthroplasty with a Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery approximately one year after implantation due to PE liner breakage. The patient experienced progressively worsening pain during extreme abduction/adduction, and radiographs demonstrated progressive ossifications at the base of the implant.

  Patient problems: Extraskeletal ossification; Implant Pain

  MAUDE report 50725366 ↗
• InjuryApr 23, 2026Break

  IT WAS REPORTED THAT A PATIENT UNDERWENT A SECOND TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2025. SUBSEQUENTLY, THE PATIENT UNDERWENT A THIRD REVISION SURGERY ON (B)(6) 2026 DUE TO PAIN AND POLYETHYLENE LINE BREAKAGE. THE SURGEON DID A SYNOVECTOMY, REMOVAL OF METALLOSIS, REPLACED THE CUP AND THE NECK. ADDITIONALLY, 2-3 MM WERE RESECTED FROM THE TRAPEZIAL SURFACE AND PLACED A NEW CUP IN A NEW BONE BED DEEPER.

  Patient problems: Implant Pain; Metal Related Pathology; Synovitis

  MAUDE report 24966090 ↗
• InjuryApr 17, 2026Break; Mechanical Jam; Migration

  IT WAS REPORTED THAT A PATIENT UNDERWENT TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2025. SUBSEQUENTLY, THE PATIENT UNDERWENT A REVISION SURGERY ON (B)(6) 2026. THE PATIENT ALLEGED IN (B)(6) 2026 PAIN AND RESTRICTED MOVEMENT IN THE OPERATED THUMB, 13 MONTHS AFTER IMPLANTATION.

  Patient problems: Implant Pain; Loss of Range of Motion

  MAUDE report 24912704 ↗