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Recall Observatory FDA recall evidence

Device product

BD MAXTM Vaginal Panel. Catalog Number(s): 443712 443710 443711 (RUO)for collection and transport of vaginal and endocervical swab specimens, in addition to the preservation of urine from males and females.

Z-0392-2018

July 18, 2017

Class II

Product summary

Firm
Becton Dickinson & Co.
Event
Event 78808
Status
Terminated
Classification
Class II
Quantity
N/A
Official record key
device-enforcement:Z-0392-2018

Official wording

Reason: BD recently notified customers in July 2017 regarding an increased rate of unresolved (UNR) and indeterminate (IND) results for the BD MAXTM Vaginal Panel, experienced by some customers. A non-reportable result may lead to repeat of the test and/or re-collection of a specimen.

Code information: UDI: 30382904433766. All Lot numbers: Not Distributed in US Not Distributed in US

Distribution pattern: US and OUS.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    BD recently notified customers in July 2017 regarding an increased rate of unresolved (UNR) and indeterminate (IND) results for the BD MAXTM Vaginal Panel, experienced by some customers. A non-reportable result may lead to repeat of the test and/or re-collection of a specimen.