NEUFLEX 1234-20-000Recalls & reported problems
Depuy Orthopaedics, Inc. · NEUFLEX MCP FINGER IMPLANT 20 CEMENTLESS · Class 2 · Implant
Data updated Oct 18, 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 10603295017967), received between Aug 4, 2017 and Aug 4, 2017 — classified as 1 injury.
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 18, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 4, 2017Break; Break
DER STATES THAT PATIENT IS VERY ACTIVE IN HORSEBACK RIDING, CLEANING STALLS, ETC. SURGEON FELT PATIENT HAD DISRUPTED HER COLLATERAL LIGAMENTS AND TOOK IN FOR REPAIR. SURGEON FOUND DISRUPTED COLLATERALS BUT ALSO 3 OF 4 MCP NUFLEX IMPLANTS (INDEX, MIDDLE, RING) HAD BROKEN AT THE POST. TWO OF THESE (INDEX/MIDDLE) HAD BEEN IMPLANTED ON (B)(6) 2013. THE RING SURGEON HAD REVISED AND IMPLANTED NEW ON (B)(6) 2016. SURGEON. BELIEVED IMPLANT FAILURE DUE TO IMPLANT POSTPONING EXASPERATED BY COLLATERAL LIGAMENT FAILURE.
Patient problems: No Information
MAUDE report 6766997 ↗
Other PROSTHESIS, FINGER, CONSTRAINED, POLYMER devices
- Osteotec Silicone Finger Implant - Size 4 OSTF-4Osteotec Limited · Prosthesis, Finger, Constrained, Polymer1 recall1 report
- Osteotec Silicone Finger Implant - Size 3 OSTF-3Osteotec Limited · Prosthesis, Finger, Constrained, Polymer1 recall0 reports
- Osteotec Silicone Finger Implant - Size 5 OSTF-5Osteotec Limited · Prosthesis, Finger, Constrained, Polymer1 recall0 reports
- NA PIP-30Stryker GmbH · PROSTHESIS, FINGER, CONSTRAINED, POLYMER27 reports
- NA PIP-20Stryker GmbH · PROSTHESIS, FINGER, CONSTRAINED, POLYMER21 reports
- NA MCP-30Stryker GmbH · PROSTHESIS, FINGER, CONSTRAINED, POLYMER16 reports
- NA PIP-10Stryker GmbH · PROSTHESIS, FINGER, CONSTRAINED, POLYMER16 reports
- NA MCP-50Stryker GmbH · PROSTHESIS, FINGER, CONSTRAINED, POLYMER14 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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