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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:138382

Medical Device Exchange Insufflation Needle; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number C2201; EXP (repackager), Medline (OEM) Insufflator, laparoscopic

Official recall number

Z-2232-2015

Evidence summary

Product code
HIF
Recall status
Terminated
Event initiated
February 11, 2015
Root cause
Other
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2232-2015

Field note

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