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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:157190

Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment or prevention of disease, or to affect the structure or any function of the body.

Official recall number

Z-2804-2017

Evidence summary

Product code
KZH
Recall status
Terminated
Event initiated
June 23, 2017
Root cause
Under Investigation by firm
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2804-2017

Field note

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