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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:180012

REF: B90240-50, 96" (244 cm) Appx 11.2 ml, 10 Drop Admin Set w/Coiled Tubing, Pre-Slit Port, Clave, Rotating Luer, Sterile R, UDI: (01)00887709077058

Official recall number

Z-1913-2020

Evidence summary

Product code
FMG
Recall status
Terminated
Event initiated
October 04, 2019
Root cause
Mixed-up of materials/components
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1913-2020

Field note

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