SR PIP SR PIP-4Recalls & reported problems
Stryker GmbH · Proximal Interphalangeal Implant, Size 4 · Class f · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00886385020341), received between Jul 20, 2021 and May 7, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
- Loss of Osseointegration1
Patient problems
- Failure of Implant1
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 7, 2026Insufficient Device Problem Information
REVISION SURGERY DUE TO REMOVED PROXIMAL SIDE / UNKNOWN REVISION REASON.
Patient problems: Insufficient Information
MAUDE report 25112365 ↗InjuryJul 20, 2021Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THE COMPONENT WAS LOOSE; REVISION SURGERY WAS PERFORMED.
Patient problems: Failure of Implant
MAUDE report 12198392 ↗
Other Semi-Constrained Metal/Polymer Finger Joint Prosthesis devices
- SR PIP SR PIP-3Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis5 reports
- SR MCP 5800-MD00Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis5 reports
- SR PIP 17-1325Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis3 reports
- SR MCP 5800-LG00Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis3 reports
- SR MCP 5800-XL00Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis2 reports
- SR PIP SR PIP-1Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis2 reports
- SR PIP 17-1327Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis2 reports
- SR PIP SR PIP-2Stryker GmbH · Semi-Constrained Metal/Polymer Finger Joint Prosthesis2 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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