Skip to content

5008X HDF Hemodialysis Blood Tubing Set with CLiC Blood Chamber 03-5100-7CRecalls & reported problems

Fresenius Medical Care Renal Therapies Group, LLC · 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
1

Summary

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

1 FDA recall record 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. Apr 29, 2025Class IIOpen, Classified

    Potential of blood leak occurring between the lower port of the venous chamber and the tubing include: hemodiafiltration (HDF), hemodialysis (HD), hemofiltration (HF), and isolated ultrafiltration.

    Z-1992-2025 · Root cause: Process control · Recall details · FDA record ↗

Other Accessories, Blood Circuit, Hemodialysis devices

All Accessories, Blood Circuit, Hemodialysis devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page