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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:139591

Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters are packaged in film-to-film pouches and packaged 30 per box. Used as an Intermittent Urinary Catheter

Official recall number

Z-2732-2015

Evidence summary

Product code
KOD
Recall status
Terminated
Event initiated
August 24, 2015
Root cause
Unknown/Undetermined by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2732-2015

Field note

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