MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-03 for GAIT BELT manufactured by Posey, S. De R.l. De C.v..
[177370137]
Two new gait belts. Multiple staff reporting that the buckle/clasp slips and fails to hold the patient securely when under tension. Owens and minor (tan) gait belt
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9659199 |
| MDR Report Key | 9659199 |
| Date Received | 2020-02-03 |
| Date of Report | 2019-12-02 |
| Date of Event | 2019-11-26 |
| Report Date | 2019-12-03 |
| Date Reported to FDA | 2019-12-03 |
| Date Reported to Mfgr | 2020-02-03 |
| Date Added to Maude | 2020-02-03 |
| 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 | OTHER HEALTH CARE PROFESSIONAL |
| 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 | GAIT BELT |
| Generic Name | RESTRAINT, PROTECTIVE |
| Product Code | FMQ |
| Date Received | 2020-02-03 |
| Lot Number | 9253T070 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | POSEY, S. DE R.L. DE C.V. |
| Manufacturer Address | 272 EAST DEERPATH ROAD SUITE 206 LAKE FOREST IL 60045 US 60045 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-02-03 |