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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:188608

Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.

Official recall number

Z-2285-2021

Evidence summary

Product code
NGT
Recall status
Open, Classified
Event initiated
August 04, 2021
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2285-2021

Field note

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