TOUCH® CMC 1 NTO08Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 07640181160020), received between Nov 11, 2025 and Sep 25, 2026 — classified as 11 injuries.

The most frequently reported specific device problem is “Mechanical Jam” (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 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• InjuryJul 21, 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, APPROXIMATELY 2 WEEKS POST-SURGERY DUE TO DISLOCATION; THE PATIENT REPORTEDLY DISLOCATED THE PROSTHESIS WHILE REMOVING A PLASTIC BAG THAT HAD BEEN PLACED OVER THE HAND DURING SHOWERING.

  Patient problems: Joint Dislocation

  MAUDE report 25890507 ↗
• InjuryJul 7, 2026Inadequacy of Device Shape and/or Size

  PT RETURNED FOR 2 WEEK POST-OP VISIT AND WAS DISLOCATED. DR (b)(6) STATED THAT HE FELT LIKE THE ORIGINAL NECK (08) WAS TOO TIGHT AND CAUSED A VOLAR DISLOCATION. PT TAKEN BACK TO SURGERY ON (B)(6). ORIGINAL NECK (NTO08) WAS REPLACED WITH A (NTO06).

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 25733794 ↗
• InjuryJun 16, 2026Adverse Event Without Identified Device or Use Problem

  I WAS REPORTED THAT TWO WEEKS POST REVISION, THE PATIENT LIFTED HIS GRANDCHILD AND THE DEVICE DISLOCATED. THE SURGEON PERFORMED A CLOSED REDUCTION AT HIS UNDER FLUOROSCOPY; HOWEVER, THE PATIENT REPORTED THAT THE DEVICE FELT UNSTABLE AND WAS "POPPING OUT." THE SURGEON NOTED THAT THE PATIENT WAS NOT COMPLIANT WITH ACTIVITY RESTRICTIONS (E.G., VACUUMING, TAE-KWON-DO ARM STRETCHES) AND HAD REMOVED THE POST-INITIAL IMPLANTATION SOFT WRAP PREMATURELY. THE SURGEON DECIDED TO PERFORM A REVISION AND OBSERVED LAXITY IN THE JOINT SPACE, BUT HE CONFIRMED THAT BOTH THE CUP AND THE STEM WERE STABLE.

  Patient problems: Failure of Implant

  MAUDE report 25522990 ↗
• InjuryJun 12, 2026Device Dislodged or Dislocated

  I WAS REPORTED THAT A PATIENT UNDERWENT A JOINT ARTHROPLASTY ON (B)(6) 2026. TWO WEEKS POST REVISION, THE PATIENT LIFTED HIS GRANDCHILD AND THE DEVICE DISLOCATED. THE SURGEON PERFORMED A CLOSED REDUCTION AT HIS UNDER FLUOROSCOPY; HOWEVER, THE PATIENT REPORTED THAT THE DEVICE FELT UNSTABLE AND WAS "POPPING OUT." THEREFORE, THE PATIENT UNDERWENT REVISION SURGERY AND THE SURGEON AND OBSERVED LAXITY IN THE JOINT SPACE; THE NECK WAS REVISED.

  Patient problems: Joint Dislocation

  MAUDE report 25484781 ↗
• InjuryApr 1, 2026Break; Material Deformation; Mechanical Jam; Naturally Worn

  IT WAS REPORTED THAT A PATIENT UNDERWENT TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2023. SUBSEQUENTLY, THE PATIENT HAD A FALL 18 MONTHS POST INITIAL SURGERY AND DURING A WRIST ARTHRODESIS PROBLEMS WITH THE PROSTHESIS WERE NOTED. THEREFORE, THE PATIENT UNDERWENT A REVISION SURGERY ON (B)(6) 2026.

  Patient problems: Loss of Range of Motion; Metal Related Pathology

  MAUDE report 24757021 ↗
• InjuryMar 23, 2026Break; Material Deformation; Mechanical Jam

  IT WAS REPORTED THAT A PATIENT UNDERWENT TOTAL JOINT ARTHROPLASTY WITH A TOUCH CMC1 PROSTHESIS ON (B)(6) 2025. IN (B)(6) 2025, THE PATIENT NOTED A CRACKING OR RUPTURE-LIKE SOUND ACCOMPANIED BY A MINIMAL AMOUNT OF BLEEDING. SUBSEQUENTLY, ON (B)(6) 2026, THE PATIENT UNDERWENT A REVISION PROCEDURE DURING WHICH THE NECK COMPONENT WAS REPLACED. NO TRAUMA WAS REPORTED IN ASSOCIATION WITH THE EVENT.

  Patient problems: Joint Impingement

  MAUDE report 24662925 ↗
• InjuryMar 10, 2026Material Deformation

  IT WAS REPORTED THAT A 60-YEAR-OLD MALE PATIENT UNDERWENT A REVISION SURGERY OF TOUCH CMC1 PROSTHESIS ON (B)(6) 2026, 6 MONTHS AFTER THE INITIAL IMPLANTATION, DUE TO CREPITATION THAT HAD DEVELOPED. DURING THE PROCEDURE, THE SURGEON REPLACED THE NECK COMPONENT.

  Patient problems: Extraskeletal ossification; Joint Impingement

  MAUDE report 24557557 ↗
• InjuryFeb 27, 2026Fracture

  A TOUCH CMC 1 NECK COMPONENT (NTO08) EXPLANT WAS RECEIVED FOLLOWING A REVISION SURGERY PERFORMED AT (B)(6) IN (B)(6) 2025. NO CLINICAL SIGNS, SYMPTOMS OR CONDITIONS WERE REPORTED BY THE HEALTH ESTABLISHMENT. AFTER THREE ATTEMPTS, NO ADDITIONAL INFORMATION RELATED TO THIS EVENT WAS COMMUNICATED.

  Patient problems: Insufficient Information

  MAUDE report 24471095 ↗
• InjuryFeb 16, 2026Device Dislodged or Dislocated; Mechanical Jam

  IT WAS REPORTED THAT A PATIENT UNDERWENT TOTAL JOINT ARTHROPLASTY ON (B)(6) 2025. SUBSEQUENTLY, ON (B)(6) 2026, THE PATIENT UNDERWENT A REVISION DUE TO A WORKPLACE ACCIDENT, INVOLVING AN AXIAL IMPACT TO THE THUMB, FOLLOWED BY A LOCKING SENSATION WITH INABILITY TO MOBILIZE THE JOINT AND ASSOCIATED PAIN. DURING THE REVISION PROCEDURE, IN ADDITION TO REPLACING THE LINER, THE SURGEON PERFORMED SLIGHT OSTEOPHYTE REDUCTION.

  Patient problems: Implant Pain; Joint Impingement

  MAUDE report 24345203 ↗
• InjuryNov 11, 2025Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE PATIENT CAME IN CONSULTATION BECAUSE OF PAIN AND DISCOMFORT SINCE A FEW MONTHS. HE UNDERWENT A REVISION SURGERY 24 MONTHS POST OPERATIVE. REVISION REVEALED NO METALLOSIS BUT THE PE LINER IS VISUALLY DAMAGED. SURGEON RESECTED BONE AND PLACED A NEW NECK NTO08.

  Patient problems: Extraskeletal ossification; Implant Pain; Joint Impingement

  MAUDE report 23520965 ↗