TOUCH® CMC 1 STO2Recalls & 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
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07640181160136), received between Jun 12, 2026 and Jun 12, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination” (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
- Contamination1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 12, 2026Contamination
IT WAS REPORTED THAT DURING A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1, AFTER THE STEM WAS IMPACTED, THE SURGEON OBSERVED A PIECE OF PLASTIC AT THE BASE OF THE STEM. THE SURGEON REMOVED THE FRAGMENT AND THEN PROCEEDED TO COMPLETE IMPLANTATION OF THE STEM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25485872 ↗
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
- TOUCH® CMC 1 NTO010Keri Medical SA · Prosthesis, Finger, Semi-Constrained, Metal/Polymer4 reports
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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