SLR BIPOLAR 17002802Recalls & reported problems
Microport Orthopedics Inc. · SLR BIPOLAR INSERT 41-44mm X 28mm ID · Class 2 · Implant
Data updated Oct 18, 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 M684170028021), received between Jan 2, 2020 and Sep 4, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).
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
- Device Dislodged or Dislocated2
Patient problems
- Insufficient Information1
- No Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 4, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT CAME IN FOR ROUTINE POST-OP EXAMINATION ON (B)(6) 2023. X-RAYS WERE TAKEN AND IT WAS FOUND THAT THE PATIENT'S GLENOSPHERE HAD COMPLETELY DISLOCATED FROM THE LINER. NO DISCOMFORT OR LOSS OF UTILITY WAS REPORTED AND NO INCIDENT WAS IDENTIFIED WHICH COULD HAVE CAUSED THE DISLOCATION. THE LINER WAS REPLACED WITH A NEW SLR LINER ON (B)(6) 2023. (B)(4).
Patient problems: Insufficient Information
MAUDE report 17676585 ↗InjuryJan 2, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT DISLOCATED THE CONSTRAINED CUSTOM IMPLANT A MONTH AFTER REVISION SURGERY.
Patient problems: No Information
MAUDE report 9540131 ↗
Other Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented devices
- STAGEONE 431209Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 recalls0 reports
- SELF CENTERING 1035-45-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented84 reports
- LFIT 6260-9-036Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented80 reports
- ACTIS 101011060Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented66 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165228Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall1 death12 reports
- SELF CENTERING 1035-44-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented60 reports
- TANDEM 71324046Smith & Nephew, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall9 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145170Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented59 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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