Medtronic Xomed, Inc. 2022-06-08 Health serious FDA
Health · FDA · Recall #FDA-Z-1224-2022
NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2 Recall
Issued June 8, 2022 · Medtronic Xomed, Inc.
In June 2022, Medtronic Xomed, Inc. recalled the NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Software anomaly was identified.
What you should do
- 1 Stop using NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medtronic Xomed, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Medtronic Xomed, Inc.
- Category
- Health
- Recall date
- June 8, 2022
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide distribution in the states of TX, CO, NJ and the country of France.
- Recall number
- FDA-Z-1224-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Medtronic Xomed, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.