Sklar 96-2237MRecalls & reported problems
Sklar Corporation · VIENNA NSL SPEC MD STRL CS/25 · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Dec 3, 2024Open, Classified
Reports of various packaging issues that may result in a breach of the sterile barrier.
Z-0930-2025 · Root cause: Under Investigation by firm · FDA record ↗
Other SPECULUM, ENT devices
- Sklar 96-2238Sklar Corporation · SPECULUM, ENT1 recall0 reports
- Centurion I68505Centurion Medical Products Corporation · SPECULUM, ENT1 recall0 reports
- Sklar 96-2236Sklar Corporation · SPECULUM, ENT1 recall0 reports
- Integra® Jarit® 400143Integra Lifesciences Production Corporation · SPECULUM, ENT1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.