TOUCH® CMC 1 NTO156Recalls & reported problems

Summary

The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 07640181160044), received between Nov 11, 2025 and Sep 28, 2026 — classified as 18 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (5 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 18 most recent of 18 reports, in the reporter's own words as published by the FDA.

• 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, 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 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, 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 ↗
• InjuryAug 6, 2026Fracture; Noise, Audible

  Patient problems: Metal Related Pathology

  MAUDE report 50165388 ↗
• InjuryJun 29, 2026Break; Malposition of Device

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS. SUBSEQUENTLY, THE PATIENT UNDERWENT REVISION SURGERY DUE TO OFF-CENTER POSITIONING OF THE NECK AND METALLOSIS, WHICH LED TO THE FORMATION OF TWO CYSTS.

  Patient problems: Cyst(s); Metal Related Pathology

  MAUDE report 25651954 ↗
• InjuryJun 24, 2026Defective Device; Device Dislodged or Dislocated

  IT WAS REPORTED THAT A PATIENT UNDERWENT TOUCH CMC1 REVISION SURGERY ON (B)(6) 2026, DUE TO DISLOCATION AND DEFECTIVE PE LINER.

  Patient problems: Joint Dislocation

  MAUDE report 25607932 ↗
• InjuryJun 17, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2024. SUBSEQUENTLY, THE PATIENT REPORTED PAIN IN THE METACARPAL-INTERNAL TRAPEZIUM AREA. THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2026. AN OSTEOPHYTE WAS OBSERVED, WHICH HAD NOT BEEN PRESENT AT THE TIME OF THE INITIAL IMPLANTATION. DURING THE NECK REVISION, THE SURGEON RESECTED OSTEOPHYTES AND SOFT TISSUES, AND CONFIRMED THAT NO IMPINGEMENT WAS PRESENT. IT WAS ALSO REPORTED THAT THE CUP WAS STILL SECURELY IN PLACE, WITH A SMALL TRACE OF METALLOSIS.

  Patient problems: Extraskeletal ossification; Implant Pain; Metal Related Pathology

  MAUDE report 25532951 ↗
• InjuryMay 29, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2021. SUBSEQUENTLY, THE PATIENT UNDERWENT REVISION SURGERY ON (B)(6), 2026, DUE TO DUE TO OSSIFICATION, BONE REGROWTH NOTED BY THE SURGEON, AND JOINT STIFFNESS AND BLOCKAGE.

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

  MAUDE report 25333351 ↗
• InjuryMay 6, 2026Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION OF A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS FIVE YEARS LATER DUE TO A PE FRACTURE, DURING WHICH SIGNIFICANT METALLOSIS WAS IDENTIFIED, ULTIMATELY LEADING TO A TRAPEZIECTOMY.

  Patient problems: Joint Impingement; Metal Related Pathology

  MAUDE report 25099711 ↗
• InjuryApr 23, 2026Deformation Due to Compressive Stress; Device Dislodged or Dislocated; Mechanical Jam

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT UNDERWENT A REVISION SURGERY ON AN UNKNOWN DATE, DUE TO UNKNOWN REASONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Impingement

  MAUDE report 24966094 ↗
• InjuryApr 9, 2026Fracture

  IT WAS REPORTED THAT A 48-YEAR-OLD MALE PATIENT (HEATING ENGINEER) UNDERWENT A REVISION SURGERY DUE TO PAINFUL CRACKLING DURING MOVEMENT AND WHEN USING THE THUMB, NEARLY TWO YEARS POST INITIAL IMPLANTATION ((B)(6) 2023). DURING THE REVISION SURGERY, THE PE LINER WAS FOUND FRACTURED IN 2 PARTS. THE SURGEON REPLACED THE SHORT OFFSET NECK WITH A STRAIGHT ONE.

  Patient problems: Implant Pain

  MAUDE report 24831490 ↗
• InjuryMar 30, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A TOTAL JOINT ARTHROPLASTY ON (B)(6) 2026. SUBSEQUENTLY, THE PATIENT UNDERWENT FOR A REVISION SURGERY ON (B)(6) 2026, DUE TO A TRAUMATIC INJURY, A HARD FALL 1 WEEK POST INITIAL SURGERY. DURING THE REVISION SURGERY, IT WAS NOTED THAT THE IMPLANT DISLOCATED VOLARLY.

  Patient problems: Aseptic loosening

  MAUDE report 24716987 ↗
• InjuryJan 16, 2026Fracture

  IT WAS REPORTED THAT A 48-YEAR-OLD MALE PATIENT (HEATING ENGINEER) UNDERWENT A REVISION SURGERY DUE TO PAINFUL CRACKLING DURING MOVEMENT AND WHEN USING THE THUMB, NEARLY TWO YEARS POST INITIAL IMPLANTATION ((B)(6) 2023). DURING THE REVISION SURGERY, THE PE LINER WAS FOUND FRACTURED IN 2 PARTS. THE SURGEON REPLACED THE SHORT-OFFSET NECK WITH A STRAIGHT ONE.

  Patient problems: Implant Pain

  MAUDE report 24091293 ↗
• InjuryNov 18, 2025Device Dislodged or Dislocated; Insufficient Device Problem Information; Device Dislodged or Dislocated; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO PAIN 5 YEARS AFTER IMPLANTATION. DURING THE PROCEDURE, A SIGNIFICANT RECURRENCE OF OSTEOPHYTES WAS OBSERVED. AFTER DEBRIDEMENT, THE SURGEON REPLACED THE NECK.

  Patient problems: Extraskeletal ossification; Implant Pain

  MAUDE report 23579724 ↗
• InjuryNov 11, 2025Fracture; Mechanical Jam; Fracture; Mechanical Jam

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A SECOND REVISION (ON (B)(6) 2024) DUE TO PE LINER FRACTURE. A THOROUGH DEBRIDEMENT WAS CARRIED OUT DUE TO SIGNIFICANT METALLOSIS. THE CUP WAS CHANGED AND REPOSITIONED WITH A SIZE 9 CUP TO ACHIEVE BETTER CENTERING. THE NECK WAS REPLACED WITH AN NTO08.

  Patient problems: Joint Impingement; Metal Related Pathology

  MAUDE report 23520969 ↗