V. Mueller GL31Recalls & reported problems
Steris Corporation · V. Mueller PEDERSON VAGINAL SPECULA MEDIUM 4 X 7/8 inches 10.2 X 2.2CM · 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
- Mar 16, 2023Open, Classified
A portion of the two products were incorrectly marked (etched) and packaged resulting in a product mismatch. The labels and laser etchings were switched on the two products.
Z-1421-2023 · Root cause: Labeling mix-ups · FDA record ↗
Other SPECULUM, VAGINAL, METAL devices
- V. Mueller GL11Steris Corporation · SPECULUM, VAGINAL, METAL1 recall1 report
- Sklar Instruments 96-2605Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar® 96-3001Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar® 96-2607Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2613Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2603Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2615Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
- Sklar Instruments 96-2616Sklar Corporation · SPECULUM, VAGINAL, METAL1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.