WALKAWAY 40 PLUS
Report
- Report Number
- 2919016-2014-00028
- Event Type
- Malfunction
- Date Received
- June 27, 2014
- Date of Event
- March 27, 2014
- Report Date
- May 28, 2014
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS
- Product Code
- LRG
- PMA / PMN Number
- K911400
- Removal / Correction Number
- 2919016-06/09/14-001-C
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CT, US
- Reporter Occupation
- OTHER
Narratives
(B)(4). PRODUCT QUALITY ISSUE ASSOCIATED WITH AN INHERENT DEVICE AND/OR DEVICE COMPONENT CHARACTERISTIC THAT IS NOT SATISFACTORY AS SPECIFIC OR DELIVERED. SIEMENS HEALTHCARE DIAGNOSTICS INC. CONDUCTED A FIELD CORRECTION, INTERNAL NUMBER (B)(4). A WRITTEN CUSTOMER NOTIFICATION WAS SENT ON 06/2014 TO ALL CUSTOMERS AFFECTED NOTIFYING THEM OF THE SPRINGS CONTAINED IN THE ACCESS DOOR HINGE ASSEMBLY ON THE WALKAWAY PLUS INSTRUMENTS ARE BECOMING DETACHED CAUSING PREMATURE FAILURE OF THE HINGE ASSEMBLY AND A POTENTIAL SAFETY ISSUE FORT THE CUSTOMER. THE NOTIFICATION ALSO INCLUDES ACTIONS TO BE TAKEN BY CUSTOMERS. THE FDA SAN FRANCISCO DISTRICT OFFICE WA NOTIFIED ON 06/09/2014 OF THE REMEDIAL ACTION (REPORT NO. 2919016-06/09/14-001-C). A SIEMENS REPRESENTATIVE WILL CONTACT THE CUSTOMER OVER THE NEXT FEW MONTHS TO SCHEDULE A VISIT TO CORRECT THIS ISSUE WITH THE ACCESS DOOR HINGE.
IT WAS REPORTED THAT A BROKEN SPRING WAS OBSERVED TO A CURVED PIN AT THE BOTTOM OF THE SPRING LOAD CAUSING FAILURE OF THE DOOR ASSEMBLY. THE FAILURE OCCURRED WHILE THE INSTRUMENT DOOR WAS CLOSED. THE CUSTOMER FOUND THE SPRING FELL OUT WHEN THE DOOR WAS OPENED. NO REPORT OF ADVERSE EVENT OR INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 375949 | WALKAWAY 40 PLUS | WALKAWAY 40 PLUS | LRG | SIEMENS HEALTHCARE DIAGNOSTICS |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |