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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:144921

American Surgical Americot Blue 3/8" x 3/8" Ref Number: 20-22S Product Usage: Neurosurgical and Nonneurosurgical Sponges

Official recall number

Z-1731-2016

Evidence summary

Product code
GDY
Recall status
Terminated
Event initiated
March 31, 2016
Root cause
Packaging process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1731-2016

Field note

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