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 2020-02-24 for LIQUICHEK CARDIAC MARKERS PLUS CONTROL LT, LEVEL 1A 27104 manufactured by Bio-rad Laboratories, Inc..
Report Number | 2016706-2020-00001 |
MDR Report Key | 9745217 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2020-02-24 |
Date of Report | 2020-02-24 |
Date of Event | 2020-02-06 |
Date Mfgr Received | 2020-02-06 |
Device Manufacturer Date | 2017-11-30 |
Date Added to Maude | 2020-02-24 |
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 | MS. MARIA ZEBALLOS |
Manufacturer Street | 9500 JERONIMO ROAD |
Manufacturer City | IRVINE, CA |
Manufacturer Country | US |
Manufacturer Phone | 9981200136 |
Manufacturer G1 | BIO-RAD LABORATORIES, INC. |
Manufacturer Street | 9500 JERONIMO ROAD |
Manufacturer City | IRVINE, CA |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LIQUICHEK CARDIAC MARKERS PLUS CONTROL LT, LEVEL 1A |
Generic Name | MUITI-ANALYTE CONTROLS, ALL KINDS (ASSAYED) |
Product Code | JJY |
Date Received | 2020-02-24 |
Model Number | 27104 |
Catalog Number | 27104 |
Lot Number | 23694 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIO-RAD LABORATORIES, INC. |
Manufacturer Address | 9500 JERONIMO ROAD IRVINE, CA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-02-24 |