Perkin Elmer Specimen Gate, Screening Center. Data management of neonatal screening test results and demographics by qualified laboratory personnel in newborn screening programs.
Recall
- Recall Number
- Z-0166-2016
- Event Number
- 72013
- Firm
- Perkin Elmer Life Sciences Inc Laitun 4 Mustionkatu 6 Turku Finland
- FEI Number
- 3002808498
- Product Code
- JQP
- Status
- Terminated
- Root Cause
- Software design
- Initiated
- August 24, 2015
- Terminated
- January 21, 2021
Description
Perkin Elmer Specimen Gate, Screening Center. Data management of neonatal screening test results and demographics by qualified laboratory personnel in newborn screening programs.
It would be possible for an abnormal analytical test result value from an affected newborn to be reported with a default result interpretation of normal. The analytical test result value would be correct but the interpretation of the test result value would be incorrect.
Perkin Elmer issued the Recall Letter on 8/24/15 delivered to the customer by email .Software Services will be asked to make sure the customers receive the Recall Letter and implement the recommended corrective measures: Ensure all laboratory routine sample testing procedures are followed to avoid procedural anomalies. In the event a procedure anomaly occurs, review the final analytical result and the corresponding interpretation to confirm both are accurate before releasing the report. Once a PerkinElmer reporting error query is available, continue to run the query until the final corrective action is deployed to your site. The final corrective action will involve an installation update to the software. For further information, please contact your local PerkinElmer representative or [email protected]
US distribution to FL, GA, and NV; and Canada
6 units