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Power-Trialysis catheter 5605300Recalls & reported problems

Bard Access Systems, Inc. · 13Fr Trialysis ST 30cm Tray · Class 2

2 open recalls name 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, 2 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Aug 10, 2026Open, Classified

    this is a downstream recall of class I recall RES 98777

    Z-2984-2026 · Root cause: Material/Component Contamination · FDA record ↗

  2. May 21, 2026Open, Classified

    Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

    Z-2660-2026 · Root cause: Nonconforming Material/Component · FDA record ↗

Other CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED devices

All CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.