MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 1996-10-07 for STORZ LEIVERS MOUTH GAG FRAM-CHILD SIZE RIGHT N7537 R manufactured by Storz Instrument Company.
[27708]
The thumb lever on the mouth gag was found to be broken when the physician attempted to insert it.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1932180-1996-00091 |
| MDR Report Key | 43016 |
| Report Source | 05,06 |
| Date Received | 1996-10-07 |
| Date of Report | 1996-09-17 |
| Date of Event | 1996-09-17 |
| Date Facility Aware | 1996-09-17 |
| Report Date | 1996-09-18 |
| Date Reported to Mfgr | 1996-09-18 |
| Date Mfgr Received | 1996-09-18 |
| Date Added to Maude | 1996-10-21 |
| 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 | STORZ LEIVERS MOUTH GAG FRAM-CHILD SIZE RIGHT |
| Generic Name | MOUTH GAG |
| Product Code | KBN |
| Date Received | 1996-10-07 |
| Model Number | NA |
| Catalog Number | N7537 R |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 43990 |
| Manufacturer | STORZ INSTRUMENT COMPANY |
| Manufacturer Address | 499 SOVEREIGN COURT MANCHESTER MO 63011 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1996-10-07 |