MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,06 report with the FDA on 2006-12-07 for ARCHITECH LH 6C25-21 manufactured by Abbott Laboratories.
[554534]
The customer states that they noticed a shift in the same patient results that were higher when using the architect lh assay lot 33198m200 than with the former lot 32429m200. The customer also noted a shift in control values. No impact to patient management was reported.
Patient Sequence No: 1, Text Type: D, B5
[8051968]
This issue was identified while investigating an increase in customer complaints for upward shifts in non-abbott controls and patient samples, as well as calibration errors. Specifically, error code 1227, "assay (lh) number (641) calibration failure, fit concentration too high for cal f," may be generated, which would result in failure to obtain a valid calibration curve. Abbott has not received any reports of adverse events related to the affected lots of architect lh reagents. An investigation is in process. A final report will be submitted when the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1415939-2006-00052 |
| MDR Report Key | 795539 |
| Report Source | 01,06 |
| Date Received | 2006-12-07 |
| Date of Report | 2006-11-09 |
| Date of Event | 2006-08-07 |
| Date Mfgr Received | 2006-11-09 |
| Device Manufacturer Date | 2006-04-01 |
| Date Added to Maude | 2006-12-20 |
| 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 | 3 |
| Event Location | 0 |
| Manufacturer Contact | DR. DAVID BARCH, D-09Y6, AP6C-2 |
| Manufacturer Street | 100 ABBOTT PARK ROAD |
| Manufacturer City | ABBOTT PARK IL 600646092 |
| Manufacturer Country | US |
| Manufacturer Postal | 600646092 |
| Manufacturer Phone | 8479379328 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Remedial Action | RC |
| Previous Use Code | 3 |
| Removal Correction Number | 1415939-11/29/06-004-C |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ARCHITECH LH |
| Generic Name | CMIA FOR THE QUANTITATIVE DETERMINATION OF HUMAN LUTEINIZING |
| Product Code | CEP |
| Date Received | 2006-12-07 |
| Model Number | NA |
| Catalog Number | 6C25-21 |
| Lot Number | 33198M200 |
| ID Number | NA |
| Device Expiration Date | 2007-06-16 |
| Operator | UNKNOWN |
| Device Availability | Y |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 783117 |
| Manufacturer | ABBOTT LABORATORIES |
| Manufacturer Address | 100 ABBOTT PARK RD. ABBOTT PARK IL 600643500 US |
| Baseline Brand Name | ARCHITECH LH |
| Baseline Generic Name | CMIA FOR THE QUANTITATIVE DETERMINATION OF HUMAN LUTEINIZING |
| Baseline Model No | NA |
| Baseline Catalog No | 6C25-21 |
| Baseline ID | NA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2006-12-07 |