|
Product Description
|
Recall Class
|
FDA Recall Posting Date
|
Recalling Firm
|
Z-1692-2019 - IntelliVue MX40 Patient Monitor, Product number 865350, Service # USA: 453564262491 and 453564262511 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the Intel...
|
2
|
06/01/2019
|
Philips North America, LLC
|
Z-1695-2019 - IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All:
453564711531 and 453564711541 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to th...
|
2
|
06/01/2019
|
Philips North America, LLC
|
Z-1694-2019 - IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564615351, and 453564615371
Product Usage: Used primarily as a ...
|
2
|
06/01/2019
|
Philips North America, LLC
|
Z-1693-2019 - IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers
All other countries: 453564451791, 453564451811, 453564467721, 453564467741, 453564467761, 453564467781, 453564467801, 45356446...
|
2
|
06/01/2019
|
Philips North America, LLC
|