TOUCH CMC 1Recalls & reported problems across all models

We found 9 models of TOUCH CMC 1 by Keri Medical SA in the FDA's device registry (GUDID). Together they are named in 86 adverse event reports in the FDA's MAUDE database, received between Nov 7, 2025 and Sep 28, 2026 — classified as 85 injuries, 1 malfunction.

The most frequently reported specific device problem is “Fracture” (20 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported TOUCH CMC 1 problems

TOUCH CMC 1 models

9 models, most reported first. Each model has its own page with its reports, recalls and device details.

• TOUCH® CMC 1 NTO156

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  18 reports
• TOUCH® CMC 1 NTO158

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  18 reports
• TOUCH® CMC 1 CTO109

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  14 reports
• TOUCH® CMC 1 NTO08

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  11 reports
• TOUCH® CMC 1 CTO09

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  9 reports
• TOUCH® CMC 1 NTO1510

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  6 reports
• TOUCH® CMC 1 NTO06

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  5 reports
• TOUCH® CMC 1 NTO010

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  4 reports
• TOUCH® CMC 1 STO2

  Prosthesis, Finger, Semi-Constrained, Metal/Polymer
  1 report

Recent TOUCH CMC 1 adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjurySep 28, 2026Insufficient Device Problem Information

  Patient problems: Failure of Implant; Medical device site infection

  MAUDE report 50923447 ↗
• InjurySep 28, 2026Insufficient Device Problem Information

  Patient problems: Failure of Implant

  MAUDE report 50923023 ↗
• InjurySep 28, 2026Insufficient Device Problem Information

  Patient underwent a revision due to dislocation.Brought the patient back for a revision operation. Exchanged short offset neck for a short straight neck.

  Patient problems: Failure of Implant

  MAUDE report 50919838 ↗
• InjurySep 25, 2026Noise, Audible

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to pain and suspected clicking. During revision surgery, significant scar tissue was observed.

  Patient problems: Implant Pain

  MAUDE report 50898214 ↗
• InjurySep 25, 2026Material Deformation

  Patient problems: Metal Related Pathology

  MAUDE report 50898158 ↗
• InjurySep 25, 2026Insufficient Device Problem Information

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to pain and a creaking sensation after one year with no reported complications. No trauma was reported.

  Patient problems: Implant Pain

  MAUDE report 50898156 ↗
• InjurySep 25, 2026Insufficient Device Problem Information

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to neck impingement.

  Patient problems: Joint Impingement

  MAUDE report 50898154 ↗
• InjurySep 23, 2026Osseointegration Problem; Loosening of Implant Not Related to Bone-Ingrowth

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to pain and loosening of the cup. During revision surgery, metallosis was observed, and the stem was found deeper than at primary placement. The cup and neck were revised, and bone resection was performed.

  Patient problems: Implant Pain; Inadequate Osseointegration; Metal Related Pathology

  MAUDE report 50869257 ↗
• InjurySep 23, 2026Mechanical Jam

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to a clicking sensation experienced since shortly after the primary placement. During the revision, the neck and cup were extracted, and metallosis was observed.

  Patient problems: Metal Related Pathology

  MAUDE report 50869256 ↗
• InjurySep 22, 2026Insufficient Device Problem Information

  Patient problems: Failure of Implant; Loss of Range of Motion

  MAUDE report 50860376 ↗
• InjurySep 22, 2026Break

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient fell, and the prosthesis was dislocated. During revision surgery, the PE liner was found fractured.

  Patient problems: Joint Dislocation

  MAUDE report 50856302 ↗
• InjurySep 22, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to infection. During the revision surgery, the surgeon performed a washout and neck exchange.

  Patient problems: Medical device site infection

  MAUDE report 50855031 ↗
• InjurySep 22, 2026Device Dislodged or Dislocated

  It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to dislocation. The offset neck was revised for a straight neck.

  Patient problems: Joint Dislocation

  MAUDE report 50855029 ↗
• InjurySep 18, 2026Mechanical Jam

  Patient problems: Loss of Range of Motion; Periprosthetic fracture

  MAUDE report 50821137 ↗
• InjurySep 18, 2026Migration

  Patient problems: Inadequate Osseointegration

  MAUDE report 50821128 ↗