Scorpio 82-6-0710Recalls & reported problems
Howmedica Osteonics Corp. · Tibial Bearing Insert - CR · Class 2 · Implant
All models of Scorpio (107)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327030648), received between Jun 26, 2018 and Oct 10, 2023 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Degraded” (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.
Reports received per month
Most reported problems
Device problems
- Degraded1
- Insufficient Device Problem Information1
- Mechanical Problem1
- Naturally Worn1
Patient problems
- Insufficient Information1
- No Consequences Or Impact To Patient1
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 10, 2023Degraded; Naturally Worn; Degraded; Naturally Worn
REVISION KNEE. LEFT SCORPIO NRG CR X3. OPERATION WAS POLY CHANGE, FOR WEAR. SIZE 8L FEMUR. SIZE 7 TIBIA. 7-10MM NRG CR X3 POLY. SURGEON WOULD LIKE THE WEAR ON THE CR X3 POLY INVESTIGATED. MEDIAL SIDE IN PARTICULAR, DEEPER WHITE AREA.
Patient problems: Insufficient Information
MAUDE report 17904120 ↗InjuryJul 1, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
TOTAL KNEE REPLACEMENT IN KS002 STUDY ON (B)(6) 2013. PATIENT REPORTS EXCESSIVE KNEE PAIN FROM (B)(6). TREATED WITH PHYSIOTHERAPY.
Patient problems: Pain
MAUDE report 8749145 ↗MalfunctionJun 26, 2018Mechanical Problem; Mechanical Problem
THE LOCKING WIRE WAS NOT FITTED TO THE INSERT THEREFORE, THE INSERT WAS EXCHANGED THE NEW SAME ONE AND THE OPERATION WAS CONTINUED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7637782 ↗
Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices
- ATTUNE 1506-00-005Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER589 reports
- ATTUNE 1506-00-004Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER580 reports
- JOURNEY 74012812Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER502 reports
- JOURNEY 74011856Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER438 reports
- PERSONA™ 42-5099-094-00Zimmer, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER406 reports
- JOURNEY 74011857Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER388 reports
- ATTUNE 1506-00-007Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER288 reports
- ATTUNE 1506-00-003Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER271 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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