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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:110043

Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use only. Distributed by Tri-Anium Assembled in Mexico. Usage: Delivery of Anesthesia.

Official recall number

Z-1898-2012

Evidence summary

Product code
CCK
Recall status
Terminated
Event initiated
May 30, 2012
Root cause
Packaging
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1898-2012

Field note

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