RecallDepth

cardioPAT Cardiovascular Perioperative Autotransfusion System, Model: LN 2050-110-E and Disposables: cardioPAT Replacement RBC Bags, LN 00270 cardioPAT Replacement Waste Bags, LN 00271 cardioPAT Replacement Intraoperative Suction Set, LN 00272 cardioPAT Replacement Postoperative Suction Set, LN 00273 cardioPAT cardiovascular Perioperative Autotransfusion System Disposable Set, LN 00274 cardioPAT Replacement One-Way Valve Assembly LN 00275

This recall has been terminated (originally issued November 23, 2005).

Company
Haemonetics Corporation
Recall Initiated
July 22, 2005
Posted
November 23, 2005
Terminated
May 24, 2012
Recall Number
Z-0174-06
Quantity
4 machines and 486 disposables
Firm Location
Braintree, MA
Official Source
View on FDA website ↗

Reason for Recall

Blood clotting of patient post operative while on the cardioPAT Cardiovascular Perioperative Autotransfusion System

Distribution

CA, MN, NE, TX

Lot / Code Info

All lot numbers

Root Cause

Other

Action Taken

Haemonetics issued a recall notification via Certified Mail on 7/22/05 to four user sites requesting return of the machine and all disposables received.

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