Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) Due to Device fail to detect Brady episodes, Pause (Asystole)...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) directly.
Affected Products
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
Quantity: 21,685
Why Was This Recalled?
Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's after a ride-through POR reset.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) has 198 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report