Haemonetics Corporation: 8 recalls on record

Recalls filed with 1 agency: FDA (8).

First recall on record: July 31, 2013. Most recent: February 5, 2020.

Risk classification: Class II: 8

Most recent recalls

DateAgencyProduct
February 5, 2020FDAJAPAN DISP SET, 261J, 205J, HAR - Product Usage: its related accessory components are int…Z-0900-2020
February 5, 2020FDACS5/5+ Fastpacks, 125 mL, 20¿ Res Autotransfusion Device- Product Usage: its related acce…Z-0889-2020
February 5, 2020FDACS5/5+ Fastpacks, 225 mL, 20¿ Res Autotransfusion Device - Product Usage: its related acc…Z-0890-2020
February 5, 2020FDAJAPAN CELL SAVER ELITE SET - 225ML - Product Usage: its related accessory components are …Z-0904-2020
February 5, 2020FDACS Elite Fastpack, 225 mL, 150 Res Autotransfusion Device - Product Usage: its related ac…Z-0895-2020
February 5, 2020FDAJapan DISP SET, 263J, 205J, HAR - Product Usage: its related accessory components are int…Z-0906-2020
February 6, 2019FDACell Saver Elite Processing Kit, 70 ml, Product ID: CSE-P-70 Indications for Use: The …Z-0779-2019
July 31, 2013FDATEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose System f…Z-1796-2013

Questions about this company

How many recalls does Haemonetics Corporation have?
Recalert has 8 U.S. recalls on record for Haemonetics Corporation, published between July 31, 2013 and February 5, 2020.
What was the most recent Haemonetics Corporation recall?
FDA recall Z-0900-2020, published February 5, 2020: JAPAN DISP SET, 261J, 205J, HAR - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a re…
Which agencies have handled Haemonetics Corporation recalls?
Haemonetics Corporation appears as the recalling firm in recalls from: FDA (8).

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