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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:155613

Non-Rebreather, Oxygen Mask, Adult 7 (2.1 m) Tubing, Product Code 3108-E, Product Code 3108MM, Product Code 86-106E, Product Code 86-108-E, Product Code LM-86-106, Product Code PMD06002, Product Code PMD06003

Official recall number

Z-2238-2017

Evidence summary

Product code
BYG
Recall status
Terminated
Event initiated
May 10, 2017
Root cause
Process control
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2238-2017

Field note

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