MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2015-07-10 for A HIGH RES SSP UNITRAY W/TAQ10 4729110 manufactured by Life Technologies.
[6030538]
This report is related to customer complaint (b)(4) made against allset gold a high res ssp (sku 54010d, lot 012 1608823), since this lot contains the same affected primer mix. The customer reported that the reactivity for lane 86 was negative for the a 03:20 alele when the labeling indicates the reactivity should be positive. The labeling discrepancy may lead to potentially mistyping a a 03:20 allele as an a 03:01 allele.
Patient Sequence No: 1, Text Type: D, B5
[14207413]
The investigation replicated the customer's observation 06/09/2015. The investigation concluded on 06/16/2015 and was unable to determine whether the result is related to the specific dna sample or reflective or incorrect labeling on the reactivity for the allele.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2244574-2015-00089 |
MDR Report Key | 4912879 |
Report Source | 05 |
Date Received | 2015-07-10 |
Date of Report | 2015-05-22 |
Date of Event | 2015-05-22 |
Device Manufacturer Date | 2015-02-13 |
Date Added to Maude | 2015-07-23 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | THOMAS TYRE |
Manufacturer Street | 9099 NORTH DEERBROOK TRAIL |
Manufacturer City | BROWN DEER WI 53223 |
Manufacturer Country | US |
Manufacturer Postal | 53223 |
Manufacturer Phone | 4142144025 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | A HIGH RES SSP UNITRAY W/TAQ10 |
Generic Name | TEST, QUALITATIVE FOR HLA |
Product Code | MZI |
Date Received | 2015-07-10 |
Catalog Number | 4729110 |
Lot Number | 012 1608873 1687240 |
Device Expiration Date | 2016-01-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | LIFE TECHNOLOGIES |
Manufacturer Address | BROWN DEER WI US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-07-10 |