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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:118394

The Zimmer Air Dermatome, REF 00- 8801- 001- 00 , Rx, non-sterile grafting instruments intended to provide variable graft thickness and width capabilities

Official recall number

Z-1483-2013

Evidence summary

Product code
GFD
Recall status
Terminated
Event initiated
May 07, 2013
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1483-2013

Field note

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