HOFFMANN 4933-0-180Recalls & reported problems
Stryker GmbH · Telescopic Strut Long LRF Length: 177-277mm (Red) · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 07613252610236), received between Jul 20, 2019 and Mar 25, 2024 — classified as 11 injuries.
The most frequently reported specific device problem is “Break” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break4
- Use of Device Problem4
- Device Dislodged or Dislocated2
- Disconnection2
- Detachment of Device or Device Component1
Patient problems
- Failure of Implant4
- Insufficient Information4
- No Code Available2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
InjuryMar 25, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED: "PIN/BOLT DETACHED FROM THE STRUT, THIS WAS FOUND AT THE PATIENT'S HOME (70 YEARS OLD). SURGERY DATE WAS 12/06/2023. SINCE THEN FULL WEIGHT BEARING, ON (B)(6) 2024 THE PATIENT CAME FOR A CHECK-UP, WHERE IT WAS DIAGNOSED. REMOVAL OF THE FIXATOR WAS (B)(6) 2024, THE EVENT DID NOT INFLUENCE THE RESULT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18969487 ↗InjuryFeb 7, 2024Use of Device Problem; Use of Device Problem
AS REPORTED: "THE ENTIRE EX FIX FAILED AT THE STRUTS. WIRES AND PINS ARE FINE. GONNA TAKE OFF NEXT THURSDAY.¿
Patient problems: Insufficient Information
MAUDE report 18660026 ↗InjuryFeb 7, 2024Use of Device Problem; Use of Device Problem
AS REPORTED: "THE ENTIRE EX FIX FAILED AT THE STRUTS. WIRES AND PINS ARE FINE. GONNA TAKE OFF NEXT THURSDAY.¿
Patient problems: Insufficient Information
MAUDE report 18660024 ↗InjuryFeb 7, 2024Use of Device Problem; Use of Device Problem
AS REPORTED: "THE ENTIRE EX FIX FAILED AT THE STRUTS. WIRES AND PINS ARE FINE. GONNA TAKE OFF NEXT THURSDAY.¿
Patient problems: Insufficient Information
MAUDE report 18659852 ↗InjuryFeb 7, 2024Use of Device Problem; Use of Device Problem
AS REPORTED: "THE ENTIRE EX FIX FAILED AT THE STRUTS. WIRES AND PINS ARE FINE. GONNA TAKE OFF NEXT THURSDAY.¿
Patient problems: Insufficient Information
MAUDE report 18659851 ↗InjuryApr 15, 2021Break; Break
AS REPORTED: "BROKEN HOFFMANN LRF STATIC STRUT. SURGEON REPLACED IN OFFICE".
Patient problems: Failure of Implant
MAUDE report 11670684 ↗InjuryApr 15, 2021Break; Break
AS REPORTED: "BROKEN HOFFMANN LRF STATIC STRUT. SURGEON REPLACED IN OFFICE".
Patient problems: Failure of Implant
MAUDE report 11670679 ↗InjuryApr 15, 2021Break; Break
AS REPORTED: "BROKEN HOFFMANN LRF STATIC STRUT. SURGEON REPLACED IN OFFICE".
Patient problems: Failure of Implant
MAUDE report 11670618 ↗InjuryApr 15, 2021Break; Break
AS REPORTED: "BROKEN HOFFMANN LRF STATIC STRUT. SURGEON REPLACED IN OFFICE".
Patient problems: Failure of Implant
MAUDE report 11670590 ↗InjuryJul 20, 2019Disconnection; Disconnection; Device Dislodged or Dislocated
AS REPORTED BY REP: "PATIENT CAME IN WITH RING FIXATOR WITH TWO TELESCOPIC STRUT ISSUES. ONE COMPLETELY DISCONNECTED. CONNTER PIN". THE SURGEON SWAPPED OUT THE 2 STRUTS IN HIS CLINIC THE NEXT DAY.
Patient problems: No Code Available
MAUDE report 8809867 ↗InjuryJul 20, 2019Disconnection; Disconnection; Device Dislodged or Dislocated
AS REPORTED BY REP: "PATIENT CAME IN WITH RING FIXATOR WITH TWO TELESCOPIC STRUT ISSUES. ONE COMPLETELY DISCONNECTED. CONNTER PIN." THE SURGEON SWAPPED OUT THE 2 STRUTS IN HIS CLINIC THE NEXT DAY.
Patient problems: No Code Available
MAUDE report 8809866 ↗
Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices
- PRECICE® Plating System LP4.5-DLF31Nuvasive Specialized Orthopedics, Inc. · Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component3 recalls0 reports
- R3 71364451Smith & Nephew, Inc. · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT145 reports
- DFS HA BONE SCREWS HAA60-15040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15050Biomet 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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