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
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
- TOUCH® CMC 1 NTO156Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer18 reports
- TOUCH® CMC 1 NTO158Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer18 reports
- TOUCH® CMC 1 CTO109Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer14 reports
- TOUCH® CMC 1 NTO08Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer11 reports
- TOUCH® CMC 1 CTO09Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer9 reports
- TOUCH® CMC 1 NTO06Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer5 reports
- TOUCH® CMC 1 NTO010Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer4 reports
- Stem holder 112-A32000Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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