MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-20 for CAREFUSION BD CLIPPER manufactured by Becton, Dickinson And Company.
[184275692]
Redness/abrasion noted to rlq of abdomen where shaving took place. Manufacturer response for razor/clippers, carefusion bd clipper (per site reporter). Unknown.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9859943 |
| MDR Report Key | 9859943 |
| Date Received | 2020-03-20 |
| Date of Report | 2020-02-04 |
| Date of Event | 2019-09-18 |
| Report Date | 2020-02-04 |
| Date Reported to FDA | 2020-02-04 |
| Date Reported to Mfgr | 2020-03-20 |
| Date Added to Maude | 2020-03-20 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CAREFUSION BD CLIPPER |
| Generic Name | SURGICAL RAZORS/CLIPPERS |
| Product Code | LWK |
| Date Received | 2020-03-20 |
| Device Availability | N |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BECTON, DICKINSON AND COMPANY |
| Manufacturer Address | 1 BECTON DRIVE FRANKLIN LAKES NJ 07417 US 07417 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2020-03-20 |