No image published for this recall
Medtronic Cardiac Rhythm And Heart Failure - safety alert
Official notice
26 May 2021
Last checked
26 May 2021
An official FDA notice concerns Medtronic Cardiac Rhythm And Heart Failure - safety alert. An official FDA notice concerns Medtronic Cardiac Rhythm And Heart Failure. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-05-26. Recall numbers: Z-1650-2021. Check the official notice for the complete list. Published 2021-05-26.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
2
Recall number
Z-1650-2021
Official notice
2021-05-26
The hazard
The hazard
An official FDA notice concerns Medtronic Cardiac Rhythm And Heart Failure. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-05-26. Recall numbers: Z-1650-2021. Check the official notice for the complete list.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Event Ids
Recall Numbers
Checked manually this time?
The app alerts you when a new official recall is published — no searching, no checking back.
Turn on recall alertsWhere it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Affected area 2
Company & contacts
Company & contacts
Brand: Medtronic Cardiac Rhythm And Heart Failure. Contact: Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF).
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Units affected
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
View full official noticeRelated recalls
a product listed in the official notice - safety alert
31 Aug 2016Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D) - safety alert
Medical Device Identification Cards associated with Sprint Quattro Lead, Product/CFN 6935M72 - safety alert
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
CareLink SmartSync Device Manager, Model Number 24970A - safety alert
a product listed in the official notice - safety alert
Programmers & Remote Monitoring Software Apps: 2090 CareLink Programmer - safety alert
a product listed in the official notice - safety alert
MEDTRONIC CARELINK 2090 programmer - safety alert
Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D) - safety alert
Medical Device Identification Cards associated with Sprint Quattro Lead, Product/CFN 6935M72 - safety alert
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only - safety alert
Weekly recall digest
Get next week's recalls before you need them.
One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.
The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.
This recall was published 26 May 2021. The next one won't wait for you to search.
RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.
