SR PIP SR PIP-1Recalls & reported problems
Stryker GmbH · Proximal Interphalangeal Implant, Size 1 · 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 00886385020310), received between Dec 29, 2023 and Sep 1, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
Patient problems
- Joint Dislocation1
- Joint Laxity1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 1, 2026Device Dislodged or Dislocated
InjuryDec 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
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-4Stryker 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.
How reports and recalls are matched · Editorial policy · Report an error on this page