TERUMO RADIFOCUS GUIDE WIRE M Adverse Event — Report (MDR 10003)
TERUMO RADIFOCUS GUIDE WIRE M Adverse Event — Report (MDR 10003) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TERUMO RADIFOCUS GUIDE WIRE M; Manufacturer: MEDI-TECH (BOSTON SCIENTIFIC CORP.); Report number: 10003.
| Device | TERUMO RADIFOCUS GUIDE WIRE M |
|---|---|
| Manufacturer | MEDI-TECH (BOSTON SCIENTIFIC CORP.) |
| Report number | 10003 |
| Product problem | * |
| Date received | 1994-07-21 |
| Narrative | FRACTURED WHILE BEING INSERTED IN PATIENT.INVALID DATA - REGARDING SINGLE USE LABELING OF DEVICE. PATIENT MEDICAL STATUS PRIOR TO EVENT: INVALID DATA. INVALID DATA - REGARDING MULTIPLE PATIENT INVOLVEMENT.INVALID DATA - ON DEVICE SERVICE/MAINTENANCE. NO DATA - REGARDING DATE LAST SERVICED. SERVICE PROVIDED BY: INVALID DATA. INVALID DATA - SERVICE RECORDS AVAILABILITY.INVALID DATA - REGARDING WHETH |
| Source | openFDA MAUDE (device adverse events) |
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