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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:161604

Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box, each catheter is packaged in an individual pouch. Urinary catheter.

Official recall number

Z-1308-2018

Evidence summary

Product code
EZD
Recall status
Terminated
Event initiated
September 14, 2017
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1308-2018

Field note

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