medical Class II Updated 2020-02-05

Haemonetics Corporation recalls JAPAN DISP SET, 261J, 205J, 208 - Product Usage: its related

Recalled Product

JAPAN DISP SET, 261J, 205J, 208 - 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 result of trauma. The recovered blood is processed by a centrifugation and washing procedure before pumping the red cell product to either a bag for gravity reinfusion into the patient or an extracorporeal circuit.


Hazard / Issue

Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell Saver¿ Elite¿/Elite¿ +125ml and 225ml bowl sets. Which could result in fluid being trapped inside the bowl core, causing a long empty device error message with the possibility of incomplete washing.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Catalog number/FG Item Number: 261J-SET 1. Specific Lots with Bowl Cracks (1819 Distributed) FP Lot numbers: 1118011-0119029-190124H2; 1118011-0119030-190125H1; 1118011-1118031-181226H1; 1118011-1118032-181226H1; 1118011-1118081-190124H1; 1118011-1118082-190124H1; 1118011-1118082-190124H2; 1118011-1118083-190124H2 2. Missing instructions to check for cracks in IFU All products/lost manufactured between October 2014 and October 2019.
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →