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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:148779

25 gauge VersaVit 2.0 Procedure Pack with Mid-Field Illuminator, Product/Part Number 70025S, packaged in HIPS rigid tray with a Tyvek lid sterile barrier system.

Official recall number

Z-0120-2017

Evidence summary

Product code
HQE
Recall status
Terminated
Event initiated
August 11, 2016
Root cause
Other
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0120-2017

Field note

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