V. Mueller T-0101Recalls & reported problems
Steris Corporation · SHADOW-LINE SIDE-LOADING TRANSVERSE RETRACTOR FRAME DOUBLE HINGED, 120MM RACK · Class 2
All models of V. Mueller (118)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403137198), received between Nov 3, 2021 and Nov 3, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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 16, 2026.
Most reported problems
Device problems
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 3, 2021Material Separation; Material Separation
THE RETRACTOR HAD BLADES ATTACHED TO HOLD THE WOUND OPEN. HOWEVER, APPROXIMATELY 45MINUTES INTO PROCEDURE, THE RETRACTOR LATCH CAME LOOSE AND FELL APART. INSTRUMENT IS CURRENTLY NOT FUNCTIONAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12746565 ↗
Other RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY devices
- AURORA® Surgiscope® ASX15/60Integra Lifesciences Corporation · Retractor, Self-Retaining, For Neurosurgery1 recall1 report
- SPOTLIGHT 282915560Depuy Spine, LLC · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY2 reports
- V. Mueller T-1295Steris Corporation · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- AURORA® Surgiscope® ASX15/80Integra Lifesciences Corporation · Retractor, Self-Retaining, For Neurosurgery1 report
- Aurora® Surgiscope® ASX9/100Integra Lifesciences Corporation · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- SPOTLIGHT 282918570Depuy Spine, LLC · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- Symmetry KARLIN™ 46-3191Aspen Surgical Products, Inc. · Retractor, Self-Retaining, For Neurosurgery1 report
- Symmetry KARLIN™ 46-3204Aspen Surgical Products, Inc. · Retractor, Self-Retaining, For Neurosurgery1 report
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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