Accelerate PhenoTest BC kit, Ref #10101018. The firm name on the label is Accelerate Diagnostics, Tucson, AZ. A multiplexed in-vitro diagnostic test intended for use with the Accelerate Pheno system.
FDA Recall Z-1529-2018 · Posted None
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Recalling FirmAccelerate Diagnostics Inc
Recall StatusTerminated
Product CodePRH
Date Initiated2018-03-14
Date Terminated2023-01-17
Product Quantity95 kits
Reason for Recall
The kits may produce an elevated rate of false positive calls for the Staphylococcus aureus identification probe (SAU).
Firm Action
The recalling firm contacted all customers on 3/14/2018 via telephone, and a follow-up e-mail was also sent containing a technical bulletin #TB000079, entitled Product Correction Notice, dated March 14, 2018. The notice identified the affected devices and the reason for the recall. Customers were asked to please discontinue use of and dispose of all remaining kits from the affected lots, and document the disposal by completing the 'Certificate of Kit Disposal.' Replacement kits will be provided.
Root Cause
Under Investigation by firm
Distribution Pattern
Distributed to IL, TX, CA, SC, and DE.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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