NeuroMend CNW4025Recalls & reported problems
Collagen Matrix, Inc. · Collagen Nerve Wrap 4mm (inner diameter) x 2.5cm (length) · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813954020129), received between Apr 10, 2019 and Apr 10, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Failure to Fold” (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.
Most reported problems
Device problems
- Failure to Fold1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 10, 2019Failure to Fold; Failure to Fold
IT WAS REPORTED BY THE CLINICIAN THAT DURING THE NERVE REPAIR PROCEDURE, THE PRODUCT WOULD NOT WRAP TOGETHER AS INTENDED AND WOULD ONLY FORM A "HORSE SHOE" SHAPE. THE CLINICIAN DECIDED TO USE ANOTHER PRODUCT AND THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A 15-20 MINUTE SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE DUE TO HOSPITAL POLICY.
Patient problems: No Code Available
MAUDE report 8500782 ↗
Other Cuff, Nerve devices
- Axoguard HA+ Nerve Protector AGHA36Axogen Corporation · Cuff, Nerve13 reports
- Axoguard HA+ Nerve Protector AGHA48Axogen Corporation · Cuff, Nerve6 reports
- Axoguard HA+ Nerve Protector AGHA24Axogen Corporation · Cuff, Nerve5 reports
- NeuraWrap® NW1040Integra Lifesciences Corporation · CUFF, NERVE2 reports
- VersaWrap VTP-2201Alafair Biosciences, Inc. · Cuff, Nerve2 reports
- NeuraGen® PNG230Integra Lifesciences Corporation · CUFF, NERVE2 reports
- NeuroMend CNW12025Collagen Matrix, Inc. · Cuff, Nerve1 report
- NervAlign Nerve Cuff NA-NC3040Renerve Limited · Cuff, Nerve1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page