FDA Adverse Event
Malfunction
Summary report: N
STERIS STRETCHER
MDR report key: 17533408
·
Received August 12, 2023
Report
- Report Number
- MW5140312
- Event Type
- Malfunction
- Date Received
- August 12, 2023
- Report Date
- March 21, 2012
- Manufacturer
- UNKNOWN
- Product Code
- FPO
- Report Source
- Voluntary report
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 0
ON FEBRUARY 22, 2012, STRYKER MEDICAL WAS NOTIFIED OF A POTENTIALLY REPORTABLE COMPLAINT INVOLVING A PRODUCT FOR WHICH STRYKER IS NOT THE MANUFACTURER. THE CUSTOMER REPORTED A STERIS STRETCHER, PRODUCT SERIAL NUMBER (B)(6), HAD A DRIFTING FOWLER CYLINDER AND A LEAKING JACK. PLEASE FIND ADDITIONAL CONTACT INFORMATION BELOW. N/A. 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 |
|---|---|---|---|---|---|---|---|
| 1354439 | STERIS STRETCHER | STRETCHER, WHEELED | FPO | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown |