MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2002-11-05 for AUTOREADER II 7003009 936000 manufactured by Ortho-clinical Diagnostics.
[21396578]
Customer reported that autoreader ii was showing increased amounts of negative optical density values on hbsag plates. No death or serious injury was associated with this incident. Note: during an audit of the complaint system, this complaint was determined to be a reportable event. This form is past the required 30 day reporting period.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2250051-2002-00665 |
MDR Report Key | 426864 |
Date Received | 2002-11-05 |
Date of Report | 2002-10-18 |
Date of Event | 2002-07-17 |
Date Facility Aware | 2002-07-26 |
Report Date | 2002-10-18 |
Date Reported to Mfgr | 2002-07-26 |
Date Added to Maude | 2002-11-13 |
Event Key | 0 |
Report Source Code | Distributor report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AUTOREADER II |
Generic Name | PLATE READER |
Product Code | LRH |
Date Received | 2002-11-05 |
Model Number | 7003009 |
Catalog Number | 936000 |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | 9 YR |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 415884 |
Manufacturer | ORTHO-CLINICAL DIAGNOSTICS |
Manufacturer Address | 1001 US HWY 202 RARITAN NJ 088690606 US |
Baseline Brand Name | ORTHO SUMMIT SAMPLE HANDLER |
Baseline Generic Name | SAMPLE HANDLER |
Baseline Model No | 7003009 |
Baseline Catalog No | 936400 |
Baseline ID | NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2002-11-05 |