MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00 report with the FDA on 1999-12-22 for PEDIATRIC OSTIUM PUNCH 8211.651 manufactured by Richard Wolf Gmbh.
[19084776]
The backward biting jaw of an ostium punch forceps broke in two during a sinus surgery procedure. A retrieval of the loose metal piece was done without any pt consequences reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1418479-1999-00055 |
| MDR Report Key | 256797 |
| Report Source | 00 |
| Date Received | 1999-12-22 |
| Date of Report | 1999-11-23 |
| Date of Event | 1999-11-23 |
| Date Facility Aware | 1999-11-23 |
| Report Date | 1999-11-23 |
| Date Reported to Mfgr | 1999-11-23 |
| Date Mfgr Received | 1999-11-23 |
| Device Manufacturer Date | 1999-01-01 |
| Date Added to Maude | 2000-01-03 |
| 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 |
| Manufacturer Contact | JERRY BALOK |
| Manufacturer Street | 353 CORPORATE WOODS PKWY |
| Manufacturer City | VERNON HILLS IL 60061 |
| Manufacturer Country | US |
| Manufacturer Postal | 60061 |
| Manufacturer Phone | 8479131113 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Remedial Action | OT |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PEDIATRIC OSTIUM PUNCH |
| Generic Name | PEDIATRIC OSTIUM PUNCH |
| Product Code | KTF |
| Date Received | 1999-12-22 |
| Model Number | 8211.651 |
| Catalog Number | 8211.651 |
| Lot Number | P660472 |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | 10 MO |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 248677 |
| Manufacturer | RICHARD WOLF GMBH |
| Manufacturer Address | PFORZHEIMER STR. 32 KNITTLINGEN GM D 75438 |
| Baseline Brand Name | OSTIUM PUNCH |
| Baseline Generic Name | OSTIUM PUNCH |
| Baseline Model No | 8211.651 |
| Baseline Catalog No | 8211.651 |
| Baseline ID | A-L-U |
| Baseline Device Family | ENT SURGICAL INSTRUMENT |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | N |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | Y |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1999-12-22 |