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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:126297

Oxoid Legionella Pneumo Groups 2-14, DR0802M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.

Official recall number

Z-1474-2014

Evidence summary

Product code
LIB
Recall status
Terminated
Event initiated
March 17, 2014
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1474-2014