MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-05-26 for ARCHITECT PROLACTIN 07K76-25 manufactured by A.i.d.d Longford.
[146389865]
An evaluation is in process. A follow-up report will be submitted when the evaluation is complete.
Patient Sequence No: 1, Text Type: N, H10
[146389866]
The customer stated that falsely elevated architect prolactin results were generated for a patient sample (id (b)(6)). No adverse impact to patient management was reported. Initial result >4,200. 00 miu/l, retest diluted result 6,657. 56 miu/l, retest using beckman dxi method 742 miu/l (within normal range).
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3005094123-2019-00157 |
MDR Report Key | 8643129 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-05-26 |
Date of Report | 2019-07-12 |
Date of Event | 2019-04-18 |
Date Mfgr Received | 2019-07-02 |
Device Manufacturer Date | 2018-08-09 |
Date Added to Maude | 2019-05-26 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | NOEMI ROMERO-KONDOS, RN BSN |
Manufacturer Street | 100 ABBOTT PARK ROAD DEPT. 09B9, LCCP1-3 |
Manufacturer City | ABBOTT PARK IL 600643537 |
Manufacturer Country | US |
Manufacturer Postal | 600643537 |
Manufacturer Phone | 224667-512 |
Manufacturer G1 | A.I.D.D LONGFORD |
Manufacturer Street | LISNAMUCK CO. LONGFORD |
Manufacturer City | LONGFORD NA |
Manufacturer Country | EI |
Manufacturer Postal Code | NA |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARCHITECT PROLACTIN |
Generic Name | PROLACTIN |
Product Code | CFT |
Date Received | 2019-05-26 |
Catalog Number | 07K76-25 |
Lot Number | 91148UI00 |
Device Expiration Date | 2019-08-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | A.I.D.D LONGFORD |
Manufacturer Address | LISNAMUCK CO. LONGFORD LONGFORD NA EI NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-05-26 |