Stem holder 112-A32000Recalls & reported problems
Keri Medical SA · Class 3
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 07640181160914), received between Feb 27, 2026 and Feb 27, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
MalfunctionFeb 27, 2026Break
IT WAS REPORTED THAT DURING A TOTAL JOINT ARTHROPLASTY OF TOUCH CMC1 PROSTHESIS, THE STEM HOLDER BROKE INTO TWO COMPONENTS DURING IMPACTION, WITH ONE COMPONENT REMAINING STUCK WITHIN THE FINAL STEM. ANOTHER INSTRUMENT WAS SUBSEQUENTLY USED TO IMPLANT A REPLACEMENT STEM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24471156 ↗
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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