Cable-Ready® Cable Grip System, Greater Trochanteric Reattachment (GTR) Device 401-120Recalls & reported problems
Pioneer Surgical Technology, Inc. · Integral Long Greater Trochanteric Reattachment Device (GTR) w/4 Cables, 23x121mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00846468064051), received between Jun 2, 2020 and Aug 25, 2026 — classified as 3 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
- No Apparent Adverse Event1
Patient problems
- Medical device site infection1
- No Information1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryAug 25, 2026No Apparent Adverse Event
Primary left hip procedure on (b)(6) 2016. Subsequently revised (b)(6) 2026 due to infection. Removed plate, stem, cup. Infection source unknown. Plate was taken off during stage 1 of the revision to remove all parts to clear infection.
Patient problems: Medical device site infection
MAUDE report 50436627 ↗InjuryNov 24, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL LEFT HIP ARTHROPLASTY ON (B)(6) 2024. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO INFECTION ON (B)(6) 2025. THE CPT FEMORAL STEM, CABLES, AND AVANTAGE ACETABULAR COMPONENTS WERE ALL REMOVED AND REPLACED.
Patient problems: Unspecified Infection
MAUDE report 23634084 ↗InjuryJun 2, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED TO RTI SURGICAL ON (B)(6) 2020 THAT A REVISION SURGERY HAD TAKEN PLACE DUE TO POST-OPERATIVE JOINT SWELLING. THE INDEX SURGERY WAS PERFORMED ON (B)(6) 2019. THE REVISION WAS PERFORMED ON (B)(6) 2020. THE PRODUCT IS NOT AVAILABLE FOR INSPECTION.
Patient problems: No Information
MAUDE report 10113269 ↗
Other Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component devices
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- DFS HA BONE SCREWS HAA60-15020Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-11030Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAB60-12040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-13040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-18030Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15030Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 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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