Alere i flu, Alere i, Alere Influenza A & B recall — FDA Z-2095-2015
Risk of false negative results due to microbial growth in the Sample Receiver of one lot of the Alere i Influenza A & B kit
Overview of recall records associated with Alere Scarborough, Inc. dba Binax, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Risk of false negative results due to microbial growth in the Sample Receiver of one lot of the Alere i Influenza A & B kit
High invalid rate and an increased risk of false negative results with certain lots of the Alere i Influenza A & B kit.
This page summarizes recall records in which the official source identifies Alere Scarborough, Inc. dba Binax, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.