V. MuellerRecalls & reported problems across all models
Steris Corporation · 118 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
V. Mueller models — page 2
118 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- V. Mueller SA1811SCISSORS, GENERAL, SURGICAL1 report
- V. Mueller SA1814SCISSORS, GENERAL, SURGICAL1 report
- V. Mueller SU3660RETRACTOR1 report
- V. Mueller T-0101RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- V. Mueller U-0545CATHETER AND TIP, SUCTION1 report
- V. Mueller U-0550CATHETER AND TIP, SUCTION1 report
- V. Mueller U-0572CATHETER AND TIP, SUCTION1 report
- V. Mueller T-1295RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- V. Mueller CH5916-3Electrosurgical, cutting & coagulation & accessories1 report
- V. Mueller CH5707Electrosurgical, cutting & coagulation & accessories1 report
- V. Mueller CH5707-3Electrosurgical, cutting & coagulation & accessories1 report
- V. Mueller CH06162-2INSTRUMENT, LIGATURE PASSING AND KNOT TYING1 report
- V. Mueller NL3785-009INSTRUMENT, MICROSURGICAL1 report
- V. Mueller OS1519MALLET, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- V. Mueller EBP22150-22SELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- V. Mueller LAT-0536-DG20Electrosurgical, cutting & coagulation & accessories1 report
- V. Mueller S-0088ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- V. Mueller OS8818-23RETRACTOR1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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