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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:160564

BD MAX" CT/GC/TV. Catalog Number(s): 443824,442970,443590 (RUO).for collection and transport of vaginal and endocervical swab specimens, in addition to the preservation of urine from males and females.

Official recall number

Z-0394-2018

Evidence summary

Product code
NSU
Recall status
Terminated
Event initiated
July 18, 2017
Root cause
Use error
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0394-2018

Field note

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