FLEXOR HIGH-FLEX ANSEL GUIDING SHEATH Adverse Event — Injury (MDR 1820334-2020-00871)
FLEXOR HIGH-FLEX ANSEL GUIDING SHEATH Adverse Event — Injury (MDR 1820334-2020-00871) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FLEXOR HIGH-FLEX ANSEL GUIDING SHEATH; Generic name: DYB INTRODUCER, CATHETER; Manufacturer: COOK INC.
| Device | FLEXOR HIGH-FLEX ANSEL GUIDING SHEATH |
|---|---|
| Generic name | DYB INTRODUCER, CATHETER |
| Manufacturer | COOK INC |
| Report number | 1820334-2020-00871 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, USER F |
| Narrative | OCCUPATION: NON-HEALTHCARE PROFESSIONAL. (B)(4). THIS REPORT INCLUDES INFORMATION KNOWN AT THIS TIME. A FOLLOW-UP REPORT WILL BE SUBMITTED SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE. |
| Source | openFDA MAUDE (device adverse events) |
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