MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-03 for LIQUID CARDIAC CONTROL LEVEL 3 CQ5053 manufactured by Randox Laboratories Ltd.
[123380409]
Randox has previously issued a recall for liquid cardiac control level 3 cq5053 lot 4245ck under rec334 (fda reference number z-2575-2018) on the 08 june 2018. Under this investigation all lots were evaluated for vial to vial imprecision and all met acceptance criteria. Subsequently, a customer queried the recovery of troponin t in liquid cardiac control level 2 cq5052 lot 4244ck. The deviation in precision observed is up to 12%. While this has been determined as acceptable by randox in the previous investigation it is not meeting the customer's needs. During the investigation of the customer complaint, real time data became available which indicated that the median recovered value has shifted from target. While the analyte median value is recovering in range this indicated a further issue with the product. Variation or a decrease in recovery of troponin t in a quality control material could delay reporting of results to a clinician. A delay in reporting troponin t could result in a delay in confirmatory diagnosis of myocardial infarction. This delay could result in a delay in treatment of the patient. Given recent complaints about this analyte and the critical nature in diagnosing cardiac events, a decision has been made to remove the claims for this analyte permanently.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 8020890-2018-00004 |
| MDR Report Key | 7929594 |
| Date Received | 2018-10-03 |
| Date of Report | 2018-09-25 |
| Date Added to Maude | 2018-10-03 |
| 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 | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | DR MARIA KELLY |
| Manufacturer Street | 55 DIAMOND ROAD |
| Manufacturer City | CRUMLIN, BT294QY |
| Manufacturer Country | UK |
| Manufacturer Postal | BT29 4QY |
| Manufacturer G1 | RANDOX LABORATORIES LTD |
| Manufacturer Street | 55 DIAMOND ROAD |
| Manufacturer City | CRUMLIN, NORTHERN IRELAND BT294QY |
| Manufacturer Country | UK |
| Manufacturer Postal Code | BT29 4QY |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | LIQUID CARDIAC CONTROL LEVEL 3 |
| Generic Name | LIQUID CARDIAC CONTROL LEVEL 3 |
| Product Code | JJY |
| Date Received | 2018-10-03 |
| Catalog Number | CQ5053 |
| Device Availability | * |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | RANDOX LABORATORIES LTD |
| Manufacturer Address | 55 DIAMOND ROAD CRUMLIN, NORTHERN IRELAND BT294QY UK BT29 4QY |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-10-03 |