FDA Adverse Event Malfunction Summary report: N

CAPTURE-R READY ID

MDR report key: 1557419 · Received December 11, 2009

Report

Report Number
1034569-2009-00438
Event Type
Malfunction
Date Received
December 11, 2009
Date of Event
November 12, 2009
Report Date
December 10, 2009
Manufacturer
IMMUCOR
Product Code
KSZ
PMA / PMN Number
STN 102707
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
MEDICAL TECHNOLOGIST

Narratives

Additional Manufacturer Narrative · 1

REVIEW OF PLATE IMAGES: A1- NEG REACTION/ 9 REACTION STRENGTH- VISUALLY NEG (NOTE: THERE IS A BLUE COLOR SEEN ON THE LOWER LEFT OF THIS WELL OUTSIDE OF THE SAMPLE WELL); B1-NEG REACTION/ 7 REACTION STRENGTH- VISUALLY NEG; C1-NEG REACTION/ 18 REACTION STRENGTH- CELL BUTTON PRESENT WITH A VERY SLIGHT PINK HALO; D1-NEG REACTION/ 8 REACTION STRENGTH- VISUALLY NEG; E1-NEG REACTION/ 8 REACTION STRENGTH-VISUALLY NEG; F1-NEG REACTION/ 5 REACTION STRENGTH- VISUALLY NEG; G1-NEG REACTION/ 11 REACTION STRENGTH- VISUALLY NEG; H1-NEG REACTION/ 6 REACTION STRENGTH- VISUALLY NEG; A2-NEG REACTION/ 11 REACTION STRENGTH- VISUALLY NEG; B2-NEG REACTION/ 11 REACTION STRENGTH- VISUALLY NEG; C2-NEG REACTION/ 8 REACTION STRENGTH- VISUALLY NEG; D2-NEG REACTION/ 9 REACTION STRENGTH- VISUALLY NEG; E2-NEG REACTION/ 8 REACTION STRENGTH- VISUALLY NEG; F2-NEG REACTION/ 8 REACTION STRENGTH- VISUALLY NEG. CONFIRMED THE REACTIVITY OF THE E ANTIGEN ON RETENTION CRRID, LOT ID120, WITH ANTI-E. CUSTOMER DID NOT SEND SAMPLE OR PRODUCT FOR FURTHER SEROLOGICAL TESTING.

Description of Event or Problem · 1

CUSTOMER REPORTED A PATIENT SAMPLE THAT RESULTED AS AN UNEXPECTED NEGATIVE WHEN TESTED WITH CAPTURE-R READY ID (CRRID).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAPTURE-R READY ID REAGENT RED BLOOD CELLS KSZ IMMUCOR ID120

Patients

Seq Age Sex Outcome Treatment
1 57 YR