Reported Mar 23, 2022 · Terminated
LINQ II Insertable Cardiac Monitor
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) · 8200 Coral Sea St Ne · Mounds View, MN · 55112-4391
Is this the product you have?
- LINQ II Insertable Cardiac Monitor
- Lot codes and dates
8 of 8 products
Products covered by this recall Model / number Product as published 00763000060374Serial RLB035341G ( ) 00763000060374Serial RLB051224G ( ) 00763000060374Serial RLB059666G ( ) 00763000060374Serial RLB061064G ( ) 00763000060381Serial RLB061812G ( ) 00763000060374Serial RLB066367G ( ) 00763000060374Serial RLB091638G ( ) 00763000554002Serial RLB122769G ( ) - Amount recalled
- 8 devices
Where it was sold
Why it was recalled
Devices may lose functionality due to susceptibility to moisture ingress.
This product could cause temporary or reversible health problems — stop using it.
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