| Catalog Number |
0002381 |
| Medical Device Problem Code |
False Negative Result (1225)
|
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
|
| Date of Event |
12/22/2017
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Type of Reportable Event
|
Malfunction
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Additional Manufacturer Narrative
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Immucor technical support advised the customer to retest the blood sample by manual test tube method up to the maximum permited incubation time of 30 minutes.This resolved the issue.
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|
Event or Problem Description
|
|
On (b)(6) 2017, a customer site reported an unexpectedly negative antibody screen by manual test tube method.
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Search Alerts/Recalls
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