ClearanceBrief
Recall Z-1344-2021 ยท LKN Separator, Automated, Blood Cell And Plasma, Therapeutic

Fenwal Inc

Amicus Exchange Kit - Product Usage: intended for use in the collection of blood components and mononuclear cells.

DateFeb 25, 2021
StatusTerminated
ReasonSome lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking centrifuge packs during a procedure on the Amicus Separator using therapeutic protocols only. The defect is a blood leak at the boot, elbow, or in the channel on the separation chamber of the centrifuge pack.
Root causeUnder Investigation by firm
ActionA Recall notification letter titled, "URGENT - Medical Device Recall Amicus MNC Apheresis/Exchange Disposable Kits" and form titled, Amicus Therapeutic Kits Customer Reply Form were sent to consignees on 02/25/2021 via Fed Ex Overnight Express. The consignee requested their customers to: 1) Discontinue use of the affected products immediately by checking their inventory and quarantining all affected product at their facility. They were also informed to contact Fresenius Kabi Customer Service at 800-333-6925, Prompt 1 for replacement kits to ensure additional procedures can continue. 2) Inform
Quantity2466 units
DistributionUS Nationwide distribution in the states of GA, TX, TN, MD, CA, KS, MN, MA, NM, NC, LA, CO, KY, NV, PA, UT, MI, NJ, IL, MD, OH, NY, FL.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K180615AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented
Fresenius Kabi USA,Llc, Dec 4, 2018