MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1997-08-04 for MAUMENEE-PARK SPECULUM E4007 manufactured by Storz Instrument Co..
[79840]
This eye speculum would not hold during a cataract procedure. Another speculum was used.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1932180-1997-00064 |
| MDR Report Key | 110669 |
| Report Source | 06 |
| Date Received | 1997-08-04 |
| Date of Report | 1997-07-22 |
| Date of Event | 1997-07-16 |
| Date Facility Aware | 1997-07-16 |
| Report Date | 1997-07-22 |
| Date Reported to Mfgr | 1997-07-22 |
| Date Mfgr Received | 1997-07-22 |
| Date Added to Maude | 1997-08-06 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MAUMENEE-PARK SPECULUM |
| Generic Name | EYE SPECULUM |
| Product Code | HNC |
| Date Received | 1997-08-04 |
| Model Number | NA |
| Catalog Number | E4007 |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | 3 YR |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 108688 |
| Manufacturer | STORZ INSTRUMENT CO. |
| Manufacturer Address | 499 SOVEREIGN CT. ST. LOUISE MO 63011 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1997-08-04 |