Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0115-2023 — Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT, MitraClip G4 Clip Delivery System NTW US/CDS0701-NTW, MitraClip G4 Clip Delivery System XT US/CDS0701-XT, MitraClip G4 Clip Delivery System XTW US/CDS0701-XTW. For cardiac proced

U.S. FDA — Device Enforcement · United States · 2022-09-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0115-2023
Date of alert
2022-09-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Abbott Vascular
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08717648226366
Reported risk: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip Opening While Locked, have been observed. Contributing causes may be clip locking component material properties and certain use conditions. Unsuccessful clip procedure can lead to recurrence of severe mitral regurgitation, device embolization, or tissue injury.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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