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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:114241

KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

Official recall number

Z-0421-2013

Evidence summary

Product code
CAE
Recall status
Terminated
Event initiated
November 02, 2012
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0421-2013