TOUCH® CMC 1 NTO010Recalls & 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
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07640181160037), received between Dec 5, 2025 and Sep 22, 2026 — classified as 4 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
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
- Device Dislodged or Dislocated1
- Fracture1
- Insufficient Device Problem Information1
- Mechanical Jam1
- Migration1
Patient problems
- Implant Pain2
- Loss of Range of Motion2
- Failure of Implant1
- Joint Impingement1
- Metal Related Pathology1
- Periprosthetic fracture1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjurySep 22, 2026Insufficient Device Problem Information
Patient problems: Failure of Implant; Loss of Range of Motion
MAUDE report 50860376 ↗InjurySep 18, 2026Mechanical Jam
Patient problems: Loss of Range of Motion; Periprosthetic fracture
MAUDE report 50821137 ↗InjuryJan 22, 2026Device Dislodged or Dislocated; Migration
IT WAS REPORTED THAT A FEMALE 64-YEAR-OLD PATIENT, PRESENTED FOR PAIN AND RECOGNIZED DISLOCATION OF THE NECK REPOSITIONED THROUGH THE PATIENT ITSELF, AFTER 2 YEARS AND 9 MONTHS.POST-OPERATIVE ADVICE WAS ACCORDING TO TREATMENT SCHEME AND FOLLOWED BY THE PATIENT.REVISION SURGERY OCCURRED, DURING WHICH NECK WAS EXCHANGED.
Patient problems: Implant Pain; Joint Impingement
MAUDE report 24147533 ↗InjuryDec 5, 2025Fracture; Fracture
IT WAS REPORTED THAT AFTER RECEIVING A TOUCH PROSTHESIS ON HIS LEFT HAND, THE PATIENT (A 65-YEAR-OLD MAN) HAD RECEIVED A TOUCH PROSTHESIS IN HIS RIGHT HAND IN (B)(6) 2025. HE RETURNED FOR A CHECK-UP IN (B)(6) 2025 AND THEN PRESENTED WITH PAIN AT THE END OF (B)(6) 2025. HE UNDERWENT A REVISION SURGERY ON (B)(6) 2025 WITH REPLACEMENT OF THE NECK (THE PE LINER WAS FOUND TO BE PERFORATED).
Patient problems: Implant Pain; Metal Related Pathology
MAUDE report 23726496 ↗
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 NTO1510Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer6 reports
- TOUCH® CMC 1 NTO06Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer5 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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