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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:134154

Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.

Official recall number

Z-1353-2015

Evidence summary

Product code
LMH
Recall status
Terminated
Event initiated
February 26, 2015
Root cause
Storage
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1353-2015

Field note

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