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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:183183

Integra Padgett Electric Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.

Official recall number

Z-2955-2020

Evidence summary

Product code
GFD
Recall status
Terminated
Event initiated
August 04, 2020
Root cause
Mixed-up of materials/components
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2955-2020