MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2000-09-27 for SNARE WIRE, PREPARED 72-6516 manufactured by Codman & Shurtleff, Inc..
[15028327]
Wire is reported to have snapped off at crease. Pt swallowed small portion of wire. Hospital reports no harm to pt.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1226348-2000-00069 |
| MDR Report Key | 298221 |
| Report Source | 05,06 |
| Date Received | 2000-09-27 |
| Date of Report | 2000-09-27 |
| Date of Event | 2000-09-05 |
| Date Mfgr Received | 2000-09-13 |
| Date Added to Maude | 2000-10-02 |
| 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 | 0 |
| Manufacturer Contact | MATHEW KING |
| Manufacturer Street | 325 PARAMOUNT DRIVE |
| Manufacturer City | RAYNHAM MA 01767 |
| Manufacturer Country | US |
| Manufacturer Postal | 01767 |
| Manufacturer Phone | 5088283106 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SNARE WIRE, PREPARED |
| Generic Name | SNARE, TONSIL |
| Product Code | KBZ |
| Date Received | 2000-09-27 |
| Model Number | NA |
| Catalog Number | 72-6516 |
| Lot Number | UNK |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 288669 |
| Manufacturer | CODMAN & SHURTLEFF, INC. |
| Manufacturer Address | 325 PARAMOUNT DRIVE RAYNHAM MA 02767 US |
| Baseline Brand Name | SNARE WIRE, PREPARED |
| Baseline Generic Name | SNARE, TONSIL |
| Baseline Model No | NA |
| Baseline Catalog No | 72-6516 |
| Baseline ID | NA |
| Baseline Device Family | SNARE WIRE, PREPARED |
| 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 | 1. Other | 2000-09-27 |