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TOUCH® CMC 1 NTO1510Recalls & reported problems

Keri Medical SA · Class 3 · Implant

All models of TOUCH CMC 1 (9)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
6
Deaths reported
0
Injuries reported
6
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07640181160068), received between Nov 11, 2025 and Aug 24, 2026 — classified as 6 injuries.

The most frequently reported specific device problem is “Fracture” (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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 2 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 2 reportsApr 2026: 0 reportsMay 2026: 1 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 1 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Fracture4
  • Break2
  • Device Dislodged or Dislocated2
  • Material Deformation1
  • Mechanical Jam1
  • Peeled/Delaminated1

Patient problems

  • Implant Pain3
  • Metal Related Pathology2
  • Aseptic loosening1
  • Bone Fracture(s)1
  • Extraskeletal ossification1
  • Inadequate Osseointegration1
  • Insufficient Information1
  • Joint Impingement1

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 24, 2026Fracture

    It was reported that a patient underwent a total joint arthroplasty of Touch CMC1 Prosthesis. Subsequently, the patient underwent revision surgery, due to reported pain. The PE liner was found to be fractured.

    Patient problems: Implant Pain

    MAUDE report 50416426 ↗
  • InjuryMay 6, 2026Break

    IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2024. SUBSEQUENTLY, THE PATIENT UNDERWENT A REVISION SURGERY ON (B)(6) 2026, DUE TO POLYETHYLENE (PE) LINER BREAKAGE.

    Patient problems: Insufficient Information

    MAUDE report 25099741 ↗
  • InjuryMar 30, 2026Device Dislodged or Dislocated

    IT WAS REPORTED THAT A PATIENT UNDERWENT TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON 2023 AND A REVISION SURGERY ON 2024. SUBSEQUENTLY, THE PATIENT UNDERWENT A THIRD REVISION SURGERY ON (B)(6) 2026 DUE TO PROSTHETIC DISLOCATION. DURING THE REVISION, THE NECK WAS REMOVED AND THE CUP WAS FOUND TO BE LOOSE, AND THE DORSAL CAP OF THE TRAPEZIUM WAS FRACTURED. SIGNS OF MILD METALLOSIS WERE ALSO OBSERVED. DUE TO INSUFFICIENT SPACE TO IMPLANT A NEW NECK, THE STEM WAS REMOVED, AND A PROXIMAL METACARPAL RESECTION WAS PERFORMED. A NEW STEM WAS THEN IMPLANTED.

    Patient problems: Aseptic loosening; Bone Fracture(s); Inadequate Osseointegration; Metal Related Pathology

    MAUDE report 24714984 ↗
  • InjuryMar 23, 2026Break; Fracture; Peeled/Delaminated; Material Deformation; Mechanical Jam

    IT WAS REPORTED THAT A PATIENT UNDERWENT TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2024. SUBSEQUENTLY, ON (B)(6) 2024 THE PATIENT MENTIONED EXPERIENCING A SNAGGING SENSATION WITH THE PROSTHESIS; THEREFORE, ON (B)(6) 2025, A REVISION SURGERY WAS PERFORMED DUE TO A FRACTURE OF THE POLYETHYLENE HEAD COMPONENT.

    Patient problems: Extraskeletal ossification; Joint Impingement; Loss of Range of Motion

    MAUDE report 24662670 ↗
  • InjuryNov 11, 2025Fracture; Fracture

    IT WAS REPORTED THAT A MALE PATIENT (1.90M, 120KG, CARPENTER, BORN IN 1968) CAME FOR PAIN, RUBBING AND GRINDING AT HIS RIGHT HAND. A REVISION SURGERY OCCURRED DURING WHICH THE NECK WAS REPLACED. CYSTS HAS BEEN FOUND BUT THE CUP WAS WELL FIXED.

    Patient problems: Implant Pain

    MAUDE report 23520960 ↗
  • InjuryNov 11, 2025Fracture; Device Dislodged or Dislocated; Fracture; Device Dislodged or Dislocated

    THE PATIENT EXPERIENCED MULTIPLE DISLOCATIONS FOLLOWING THE INITIAL IMPLANTATION ON (B)(6) 2022, REQUIRING SEVERAL CLOSED AND OPEN REDUCTIONS BETWEEN (B)(6) 2022 AND (B)(6) 2025, WITH PROGRESSIVE ADJUSTMENTS FROM A MEDIUM TO A LONG NECK OFFSET AND FINALLY TO A LONG NECK 0° CONFIGURATION, ALONG WITH PERIODS OF IMMOBILIZATION USING A CAST AND RIZOLOC BRACE. THE REVISION SURGERY REVEALED METALLOSIS AND CONTACT BETWEEN NECK AND CUP WITH POSSIBLE DISLOCATION. REPLACEMENT BY NECK NTO010.

    Patient problems: Implant Pain; Metal Related Pathology

    MAUDE report 23520552 ↗

Other Prosthesis, Finger, Semi-Constrained, Metal/Polymer devices

All Prosthesis, Finger, Semi-Constrained, Metal/Polymer devices →

Sources and updates

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