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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:205573

AirLife Adult Manual Resuscitator, 40" (1.0m) Oxygen Reservoir Tubing, Adult Mask, REF 2K8004

Official recall number

Z-1065-2024

Evidence summary

Product code
BTM
Recall status
Open, Classified
Event initiated
January 10, 2024
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1065-2024

Field note

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