FDA Adverse Event
Injury
Summary report: N
MEDLINE BASIC ROLLATOR FOUR-WHEELED
MDR report key: 6639583
·
Received June 12, 2017
Report
- Report Number
- MW5070389
- Event Type
- Injury
- Date Received
- June 12, 2017
- Date of Event
- March 20, 2017
- Manufacturer
- MEDLINE, INC.
- Product Code
- ITJ
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- NJ, US
- Reporter Occupation
- ATTORNEY
Narratives
Description of Event or Problem · 1
DEAR SIR/MADAM: WE REPRESENT (B)(6). I AM ENCLOSING THE COMPLETED REPORT FOR YOUR REVIEW. PLEASE LET ME KNOW IF THERE IS ANYTHING ELSE YOU NEED. CORDIALLY, (B)(6). INCIDENT ADDRESS: (B)(6). INJURY, MEDICAL ATTENTION RECEIVED. INJURY, EMERGENCY DEPARTMENT TREATMENT RECEIVED. LOCATION OF INJURY: ELBOW. TYPE OF INJURY: BREAK, FRACTURE. (B)(6).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 416650 | MEDLINE BASIC ROLLATOR FOUR-WHEELED | ROLLING WALKER | ITJ | MEDLINE, INC. | MD586850E |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR | Hospitalization |