Sklar InstrumentsRecalls & reported problems across all models
Sklar Corporation · 205 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Sklar Instruments models — page 3
205 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Sklar Instruments 96-2207ARETRACTOR, SELF-RETAINING1 recall0 reports
- Sklar Instruments 96-2208ARETRACTOR, SELF-RETAINING1 recall0 reports
- Sklar Instruments 96-2209ARETRACTOR, SELF-RETAINING1 recall0 reports
- Sklar Instruments 96-2210ARETRACTOR, SELF-RETAINING1 recall0 reports
- Sklar Instruments 96-2492ASCISSORS, GENERAL, SURGICAL1 recall0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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