MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2011-08-24 for CLINITEK STATUS+ ANALYZER CT STATUS+ manufactured by Siemens Healthcare Diagnostics, Manufacturing Ltd..
[2323377]
Customer reports five false positive hcg results and several borderline results over a 2-3 month period. No unnecessary medical procedure was performed. There was report to pt health.
Patient Sequence No: 1, Text Type: D, B5
[9259661]
Customer cleaning of the instrument is not in accordance with mfr's instructions. Customer is not operating instrument in accordance with mfr's instructions. Customer provided instructions for proper operation and cleaning of instrument.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1217157-2011-00029 |
MDR Report Key | 2228716 |
Report Source | 07 |
Date Received | 2011-08-24 |
Date of Report | 2011-07-27 |
Date of Event | 2011-07-27 |
Date Mfgr Received | 2011-07-27 |
Device Manufacturer Date | 2008-07-01 |
Date Added to Maude | 2012-06-26 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | MARK SMITH |
Manufacturer Street | 2 EDGEWATER DR. |
Manufacturer City | NORWOOD MA 02062 |
Manufacturer Country | US |
Manufacturer Postal | 02062 |
Manufacturer Phone | 7812693158 |
Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING, LTD. |
Manufacturer Street | NORTHERN ROAD |
Manufacturer City | SUDBURY, SUFFOLK MA 02062 |
Manufacturer Country | US |
Manufacturer Postal Code | 02062 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CLINITEK STATUS+ ANALYZER |
Generic Name | CLINITEK STATUS+ ANALYZER |
Product Code | LCX |
Date Received | 2011-08-24 |
Model Number | CT STATUS+ |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS, MANUFACTURING LTD. |
Manufacturer Address | NORTHERN ROAD SUDBURY, SUFFOLK CO106DX UK CO10 6DX |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2011-08-24 |