Brand

Cardiac Assist, Inc Recalls

7 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Cardiac Assist, Inc.

7Total Recalls
1Critical
803Units Affected
Jun 30, 2023Most Recent
All Recalls

Every Cardiac Assist, Inc Recall

Sorted by most recent. Click any recall for full details.

7 recalls
High RiskFDA
Cardiac Assist, Inc
LifeSPARC Pump (part number 5800-0000) contained within TandemLife LifeSPARC Priming Tray part number: 5800-1000. Note: The 5800-1000...
Medical Devices·2 affected·Jun 30, 2023
CriticalFDA
Cardiac Assist, Inc
TANDEM LIFE LivaNova LIFESPARC Controller; Controller and Accessories Model 5900-0000; Controller Only Model 5900-0001. For circulato...
Medical Devices·723 affected·Jul 21, 2022
High RiskFDA
Cardiac Assist, Inc
Protek Solo Venous Dilator Set: dilator, vessel, for percutaneous catheterization. Catalog #: 5840-2417 - LS Tandem Life Kit - V24/A17 ...
Surgical Devices·13 affected·Mar 19, 2021
High RiskFDA
Cardiac Assist, Inc
TandemHeart pump is assembled into kits: TandemLung Kit - DL31, Product: 5730-3118 - Product Usage: provides temporary extracorporeal c...
Cardiac Devices·2 affected·Mar 6, 2020
High RiskFDA
Cardiac Assist, Inc
TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A17, Product: 5710-6217 - Product Usage: provides temporary extracorpor...
Cardiac Devices·15 affected·Mar 6, 2020
High RiskFDA
Cardiac Assist, Inc
TandemHeart Pump Kit, Product: 5120-0000 - Product Usage: provides temporary extracorporeal circulatory system support with the unique a...
Cardiac Devices·10 affected·Mar 6, 2020
High RiskFDA
Cardiac Assist, Inc
TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29, Product: 5720-2916 - Product Usage: provides temporary extracorporeal ci...
Cardiac Devices·38 affected·Mar 6, 2020