PlainRecalls
FDA Devices Moderate Class II Terminated

Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003

Reported: February 8, 2017 Initiated: December 27, 2016 #Z-1109-2017

Product Description

Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003

Reason for Recall

The affected products have approximately a 91% specificity while the non-affected lots have approximately a 99% specificity. The recalling firm is aware of three customers who reported false positive results.

Details

Recalling Firm
Immuno-Mycologics, Inc
Units Affected
630 units
Distribution
Nationwide throughout the US
Location
Norman, OK

Frequently Asked Questions

What product was recalled?
Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003. Recalled by Immuno-Mycologics, Inc. Units affected: 630 units.
Why was this product recalled?
The affected products have approximately a 91% specificity while the non-affected lots have approximately a 99% specificity. The recalling firm is aware of three customers who reported false positive results.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 8, 2017. Severity: Moderate. Recall number: Z-1109-2017.