MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-05-17 for DIMENSION? DF207 SMN 10700795 manufactured by Siemens Healthcare Diagnostics Inc.
[145373127]
Mdr 2517506-2019-00204 was filed for the same event. The customer contacted the siemens customer care center (ccc) and reported a discordant elevated tacrolimus (tac) patient result obtained on a dimension exl 200 instrument. Siemens is investigating the event.
Patient Sequence No: 1, Text Type: N, H10
[145373128]
Discordant, falsely elevated tacrolimus (tac) results were obtained on a patient sample on a dimension exl 200 instrument. The discordant results were not reported to the physician(s). A discrepancy occurred between the results of a 1:2 dilution and a 1:3 dilution. There are no known reports of patient intervention or adverse health consequences due to the discordant tac results.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2517506-2019-00206 |
| MDR Report Key | 8619223 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
| Date Received | 2019-05-17 |
| Date of Report | 2019-06-25 |
| Date of Event | 2019-04-05 |
| Date Mfgr Received | 2019-05-31 |
| Device Manufacturer Date | 2018-09-24 |
| Date Added to Maude | 2019-05-17 |
| 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 | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | JAMES MORGERA |
| Manufacturer Street | 500 GBC DRIVE P.O. BOX 6101 |
| Manufacturer City | NEWARK DE 197146101 |
| Manufacturer Country | US |
| Manufacturer Postal | 197146101 |
| Manufacturer Phone | 3026318356 |
| Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS INC |
| Manufacturer Street | 500 GBC DRIVE P.O. BOX 6101 |
| Manufacturer City | NEWARK DE 197146101 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 197146101 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DIMENSION? |
| Generic Name | DIMENSION? TACROLIMUS FLEX? REAGENT CARTRIDGE |
| Product Code | MLM |
| Date Received | 2019-05-17 |
| Catalog Number | DF207 SMN 10700795 |
| Lot Number | GA9267 |
| Device Expiration Date | 2019-09-24 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS INC |
| Manufacturer Address | 500 GBC DRIVE P.O. BOX 6101 NEWARK DE 197146101 US 197146101 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-05-17 |