Nextra CHRecalls & reported problems across all models
Medartis Inc. · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 2
We found 3 models of Nextra CH by Medartis Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Mar 13, 2025 and Mar 13, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Damaged by Another Device” (1 report).
2 FDA recall records name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Nextra CH recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jan 13, 2022Terminated
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision
Z-0740-2022 · Root cause: Device Design · Recall details · FDA record ↗
- Jan 13, 2022Terminated
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision
Z-0739-2022 · Root cause: Device Design · Recall details · FDA record ↗
Most reported Nextra CH problems
Device problems
- Device Damaged by Another Device1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Nextra CH models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Nextra CH CH-STD-KTScrew, Fixation, Bone1 recall0 reports
- Nextra CH CH-MINI-KTScrew, Fixation, Bone1 recall0 reports
- Nextra CH CH-35MScrew, Fixation, Bone1 report
Recent Nextra CH adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionMar 13, 2025Use of Device Problem; Device Damaged by Another Device; Use of Device Problem; Device Damaged by Another Device
WE USED NEXTRA CH IMPLANT AND THE PROXIMAL AND MIDDLE IMPLANTS DID NOT FIT PROPERLY WITHIN EACH OTHER. THE IMPLANTS WERE SLIPPING OUT OF EACH OTHER EVERY TIME HE TRIED TO CLOSE. PROBLEM STATEMENT: IMPLANTS WOULD NOT LOCK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21594660 ↗
Other Medartis Inc. products
All Medartis Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page