BENTSON STRAIGHT FIXED CORE WIRE GUIDE Adverse Event — Injury (MDR 1820334-2020-00872)
BENTSON STRAIGHT FIXED CORE WIRE GUIDE Adverse Event — Injury (MDR 1820334-2020-00872) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BENTSON STRAIGHT FIXED CORE WIRE GUIDE; Generic name: DQX WIRE, GUIDE, CATHETER; Manufacturer: COOK INC.
| Device | BENTSON STRAIGHT FIXED CORE WIRE GUIDE |
|---|---|
| Generic name | DQX WIRE, GUIDE, CATHETER |
| Manufacturer | COOK INC |
| Report number | 1820334-2020-00872 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, USER F |
| Narrative | BLANK FIELDS ON THIS FORM INDICATE THE INFORMATION IS UNKNOWN, UNAVAILABLE, OR UNCHANGED. ADDITIONAL INFORMATION: D10, H3. THE DEVICE WILL NOT BE RETURNED. THIS REPORT INCLUDES INFORMATION KNOWN AT THIS TIME. A FOLLOW-UP REPORT WILL BE SUBMITTED SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE. THIS REPORT IS REQUIRED BY THE FDA UNDER 21 CFR PART 803 AND IS BASED ON UNCONFIRMED INFORMATION |
| Source | openFDA MAUDE (device adverse events) |
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