Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:172340

Thio Med w/Dex, Hem, Vit K (7ml) 20/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Official recall number

Z-1379-2019

Evidence summary

Product code
JSG
Recall status
Terminated
Event initiated
April 17, 2019
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1379-2019

Field note

Send feedback

We'll only use this to respond to your feedback.