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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:124950

Endo Illuminator, Synergetics, inc., 20ga, length 7.0 ft, sterile / EO, 56.02. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.

Official recall number

Z-0883-2014

Evidence summary

Product code
HQB
Recall status
Terminated
Event initiated
December 09, 2013
Root cause
Use error
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0883-2014