MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2013-12-20 for DIMENSION(R) CLINICAL CHEMISTRY SYSTEM - DF89A manufactured by Siemens Healthcare Diagnostics Inc - Glasgow.
[4120595]
Customer reported variability of recovery of qc cyclosporin a (csa). The customer reported lower results than the theoretical control mean for their low level control product. It is unknown if patient treatment was altered or prescribed due to the variable low level control recovery. There was no report of adverse health consequences as a result the variability of results.
Patient Sequence No: 1, Text Type: D, B5
[11384409]
The cause of the qc variability and low level qc out of range recovery is likely related to poor open well stability of the csa reagent. A shared chrome particle reagent in common with the dimension vista csa reagent, (b)(4), is the likely cause. Siemens healthcare diagnostics has confirmed complaints regarding variability of recovery of qc and patient results with the (b)(4) flex reagent cartridge lots 12300bb, 12318bb, and 13011bb. Internal testing has confirmed atypical performance and increases of >25% over several days for samples with csa concentrations below 125 ng/ml. Daily qc can detect performance variations in the assay. Errors are most pronounced below 125 ng/ml where maintenance therapy occurs, therefore, dosage adjustment based on a single result is extremely unlikely. Nevertheless, siemens issued an urgent medical device recall communication 13-90 to customers who had ordered these lots advising them to discontinue use and to discard the dimension vista lots.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2517506-2013-00425 |
| MDR Report Key | 3531682 |
| Report Source | 01,05,06 |
| Date Received | 2013-12-20 |
| Date of Report | 2013-11-25 |
| Date of Event | 2013-02-19 |
| Date Mfgr Received | 2013-11-25 |
| Device Manufacturer Date | 2012-11-07 |
| Date Added to Maude | 2014-03-31 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | SERVICE AND TESTING PERSONNEL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | JAMES MORGERA |
| Manufacturer Street | GLASGOW BUSINESS COMMUNITY PO BOX 6101 |
| Manufacturer City | NEWARK DE 197146101 |
| Manufacturer Country | US |
| Manufacturer Postal | 197146101 |
| Manufacturer Phone | 3026318356 |
| Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW |
| Manufacturer Street | GLASGOW BUSINESS COMMUNITY 500 GBC DRIVE |
| Manufacturer City | NEWARK DE 19714 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 19714 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DIMENSION(R) CLINICAL CHEMISTRY SYSTEM - |
| Generic Name | CYCLOSPORINE FLEX? REAGENT CARTRIDGE |
| Product Code | MKW |
| Date Received | 2013-12-20 |
| Catalog Number | DF89A |
| Lot Number | FA3312 |
| Device Expiration Date | 2013-11-08 |
| Operator | MEDICAL TECHNOLOGIST |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW |
| Manufacturer Address | GLASGOW BUSINESS COMMUNITY 500 GBC DRIVE NEWARK DE 19702 US 19702 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-12-20 |