MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-19 for DRIVE 10210-4ASM manufactured by Drive Devilbiss Healthcare.
[184069246]
Upon demonstrating rolling walker to issue to patient for home, noted to be defective requiring excessive force to close right- hand side. Replaced with a new walker, which functioned appropriately.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9853172 |
| MDR Report Key | 9853172 |
| Date Received | 2020-03-19 |
| Date of Report | 2020-02-18 |
| Date of Event | 2020-02-14 |
| Report Date | 2020-02-18 |
| Date Reported to FDA | 2020-02-18 |
| Date Reported to Mfgr | 2020-03-19 |
| Date Added to Maude | 2020-03-19 |
| 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 | DRIVE |
| Generic Name | WALKER, MECHANICAL |
| Product Code | ITJ |
| Date Received | 2020-03-19 |
| Model Number | 10210-4ASM |
| Lot Number | 5B11505 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Age | 1 DA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | DRIVE DEVILBISS HEALTHCARE |
| Manufacturer Address | 99 SEAVIEW BLVE SUITE 210 PORT WASHINGTON NY 11050 US 11050 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-19 |