UNKNOWN_MEDICAL_PRODUCT
Report
- Report Number
- 0001831750-2013-04950
- Event Type
- Malfunction
- Date Received
- May 31, 2013
- Date of Event
- May 7, 2013
- Report Date
- May 7, 2013
- Manufacturer
- STRYKER MEDICAL-KALAMAZOO
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- OTHER
Narratives
FOLLOW-UP SUBMITTED AS IT WAS DETERMINED AN INSPECTION WAS ALLEGEDLY PERFORMED BY THE CUSTOMER NOTING THE FOOT END LIFT WAS STUCK IN AN ELEVATED POSITION. WHEN CONTACTED, CUSTOMER STATED THEY HAD ALREADY PERFORMED THE REPAIR. EVALUATION PERFORMED BY CUSTOMER.
FOLLOW-UP SUBMITTED AS IT WAS DETERMINED THIS COMPLAINT WAS PREVIOUSLY REPORTED IN MEDWATCH #0001831750-2013-04955.
MANUFACTURER¿S INVESTIGATION IS STILL ONGOING; IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT WILL BE SUBMITTED.
IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT END LIFT WAS STUCK ELEVATED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT END LIFT WAS STUCK ELEVATED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT END LIFT WAS STUCK ELEVATED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 241646 | UNKNOWN_MEDICAL_PRODUCT | BED, AC-POWERED ADJUSTABLE HOSPITAL | FNL | STRYKER MEDICAL-KALAMAZOO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |