FDA Adverse Event
Malfunction
Summary report: N
MEDLINE STRETCHER
MDR report key: 17535314
·
Received August 12, 2023
Report
- Report Number
- MW5142213
- Event Type
- Malfunction
- Date Received
- August 12, 2023
- Report Date
- November 29, 2017
- Manufacturer
- MEDLINE INDUSTRIES INC.
- Product Code
- NZD
- Report Source
- Voluntary report
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 0
STRYKER MEDICAL WAS NOTIFIED OF A POTENTIALLY REPORTABLE COMPLAINT INVOLVING A PRODUCT FOR WHICH STRYKER IS NOT THE ORIGINAL EQUIPMENT MANUFACTURER OF THE REPORTED DEVICE. THE CUSTOMER ALLEGED A MEDLINE STRETCJER, SERIAL NUMBER (B)(6) HAD MALFUNCTIONING BRAKES, IV POLE AND CALF RELEASE. (B)(4). THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2)
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1355626 | MEDLINE STRETCHER | STRETCHER, PATIENT RESTRAINT | NZD | MEDLINE INDUSTRIES INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown |