HOFFMANN 4933-0-120Recalls & reported problems
Stryker GmbH · Telescopic Strut Short LRF Length: 119-161mm (Yellow) · Class 2
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 07613252610243), received between Jun 4, 2018 and Feb 4, 2026 — classified as 7 injuries, 1 malfunction.
The most frequently reported specific device problem is “Break” (7 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
- Break7
- Fracture1
Patient problems
- No Known Impact Or Consequence To Patient6
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
- No Information1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 4, 2026Fracture
IT WAS REPORTED THAT THE STRUT WAS BROKEN.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24257214 ↗InjuryJun 4, 2018Break
A PATIENT HAD AN LRF FRAME ON AND 7 OF THEIR WIRES ENDED UP BREAKING. WE REPLACED ALL OF THE WIRES AND ADDED HALF PINS AS WELL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7567252 ↗InjuryJun 4, 2018Break
A PATIENT HAD AN LRF FRAME ON AND 7 OF THEIR WIRES ENDED UP BREAKING. WE REPLACED ALL OF THE WIRES AND ADDED HALF PINS AS WELL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7567241 ↗InjuryJun 4, 2018Break
A PATIENT HAD AN LRF FRAME ON AND 7 OF THEIR WIRES ENDED UP BREAKING. WE REPLACED ALL OF THE WIRES AND ADDED HALF PINS AS WELL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7567240 ↗InjuryJun 4, 2018Break
A PATIENT HAD AN LRF FRAME ON AND 7 OF THEIR WIRES ENDED UP BREAKING. WE REPLACED ALL OF THE WIRES AND ADDED HALF PINS AS WELL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7567136 ↗InjuryJun 4, 2018Break
A PATIENT HAD AN LRF FRAME ON AND 7 OF THEIR WIRES ENDED UP BREAKING. WE REPLACED ALL OF THE WIRES AND ADDED HALF PINS AS WELL.
Patient problems: No Information
MAUDE report 7567131 ↗InjuryJun 4, 2018Break
A PATIENT HAD AN LRF FRAME ON AND 7 OF THEIR WIRES ENDED UP BREAKING. WE REPLACED ALL OF THE WIRES AND ADDED HALF PINS AS WELL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7567130 ↗InjuryJun 4, 2018Break
A PATIENT HAD AN LRF FRAME ON AND 7 OF THEIR WIRES ENDED UP BREAKING. WE REPLACED ALL OF THE WIRES AND ADDED HALF PINS AS WELL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7567113 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.