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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:175101

Kit BD Max MRSA XT; Catalog # 443461

Official recall number

Z-2334-2019

Evidence summary

Product code
NQX
Recall status
Terminated
Event initiated
July 17, 2019
Root cause
Process control
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2334-2019

Field note

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