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Amicus MNC Apheresis Kit - Double Needle X6R2326Recalls & reported problems

Fresenius Kabi AG · For Mononuclear Cell (MNC) Collection. For use with the AMICUS separator. Sterile Fluid Path. · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Feb 14, 2023Class IIOpen, Classified

    Potential for centrifuge packs to develop a stress leak for certain lots of Amicus MNC Apheresis kit and Amicus Exchange kit (Therapeutic Kits) on the Amicus Separator.

    Z-1254-2023 · Root cause: Process control · Recall details · FDA record ↗

  2. Feb 25, 2021Class IITerminated

    Some 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.

    Z-1343-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Separator, Automated, Blood Cell, Diagnostic devices

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Sources and updates

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