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 2017-07-10 for COBAS 6000 C501 MODULE 05860636001 manufactured by Roche Diagnostics.
[80013446]
Unique identifier (udi)#: (b)(4)
Patient Sequence No: 1, Text Type: N, H10
[80013447]
The customer complained of erroneous results for 1 patient sample tested for ua2 uric acid ver. 2 (ua2) on a cobas 6000 c (501) module. The initial ua2 result was "<0. 2 l" with a data flag. This result was reported outside of the laboratory. The repeat result was 3. 9 mg/dl. The repeat result was believed to be correct. The customer is not aware of any adverse event for this patient. The ua2 reagent lot number was 172896. The expiration date was not provided. The field service engineer (fse) visited the customer site. Reaction cell dust was falling into cells from rubbing the cell cover. The fse straightened the cover and checked all pump pressures, rinse volumes and probe alignments. Mechanism and air purges passed. The customer ran successful quality controls.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1823260-2017-01418 |
| MDR Report Key | 6696585 |
| Report Source | HEALTH PROFESSIONAL,USER FACI |
| Date Received | 2017-07-10 |
| Date of Report | 2017-08-05 |
| Date of Event | 2017-06-22 |
| Date Mfgr Received | 2017-06-22 |
| Date Added to Maude | 2017-07-10 |
| 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 |
| Reporter Occupation | MEDICAL TECHNOLOGIST |
| 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 | CDO |
| Date Received | 2017-07-10 |
| 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 | 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 | 2017-07-10 |
| 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 | 2017-07-10 |