MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2017-09-14 for COBAS 6000 C501 MODULE 05860636001 manufactured by Roche Diagnostics.
[86589387]
Unique identifier (udi)# (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[86589388]
The customer complained of a questionable result for ise indirect k for gen. 2 on one patient sample. The initial potassium result was 7. 7 mmol/l accompanied by a data flag. The sample was repeated on the same analyzer with a result of 7. 7 mmol/l. The repeat result was reported outside of the laboratory as there was no data flag present, but the result was questioned by a nurse. The original sample was pulled and potassium testing was repeated on another cobas 6000 c (501) module. The result obtained was 4. 4 mmol/l. The original sample was then repeated on the initial analyzer and a potassium result of 4. 4 mmol/l was obtained. A corrected report with the result of 4. 4 mmol/l was generated. There was no adverse event. The potassium electrode lot number was g-95 with an expiration date of 30-nov-2014. The field engineering specialist discovered a kinked potassium chloride line. He adjusted the line. He ran a precision check for potassium which passed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1823260-2017-01981 |
| MDR Report Key | 6864393 |
| Report Source | HEALTH PROFESSIONAL,USER FACI |
| Date Received | 2017-09-14 |
| Date of Report | 2017-10-09 |
| Date of Event | 2017-08-24 |
| Date Mfgr Received | 2017-08-25 |
| Date Added to Maude | 2017-09-14 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | NA MICHAEL LESLIE |
| Manufacturer Street | 9115 HAGUE ROAD NA |
| Manufacturer City | INDIANAPOLIS IN 46250 |
| Manufacturer Country | US |
| Manufacturer Postal | 46250 |
| Manufacturer Phone | 3175214343 |
| Manufacturer G1 | HITACHI HIGH TECH CORP. |
| Manufacturer Street | 882 ICHIGE HITACHINAKA NA |
| Manufacturer City | IBARAKI 312-8504 |
| Manufacturer Country | JA |
| Manufacturer Postal Code | 312-8504 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COBAS 6000 C501 MODULE |
| Generic Name | CLINICAL CHEMISTRY ANALYZER |
| Product Code | CEM |
| Date Received | 2017-09-14 |
| Model Number | C501 |
| Catalog Number | 05860636001 |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 0 |
| Device Event Key | 0 |
| Manufacturer | ROCHE DIAGNOSTICS |
| Manufacturer Address | 9115 HAGUE ROAD NA INDIANAPOLIS IN 462500457 US 462500457 |
| Brand Name | COBAS 6000 C501 MODULE |
| Generic Name | CLINICAL CHEMISTRY ANALYZER |
| Product Code | JJE |
| Date Received | 2017-09-14 |
| Model Number | C501 |
| Catalog Number | 05860636001 |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ROCHE DIAGNOSTICS |
| Manufacturer Address | 9115 HAGUE ROAD NA INDIANAPOLIS IN 462500457 US 462500457 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-09-14 |