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Recall Observatory FDA recall evidence

Device product

Revaclear 300 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.

Z-0762-2023

November 23, 2022

Class II

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 91223
Status
Ongoing
Classification
Class II
Quantity
14,053,824 units
Official record key
device-enforcement:Z-0762-2023

Official wording

Reason: Reports of Polyurethane Displacement in the dialyzer, and might be identified as a blood leak

Code information: UDI-DI: 07332414123055; Product Code: 114745L; All lot numbers from C419128801-C422128401

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Canada, China, Australia, New Zealand, Austria, Egypt, France, Germany, Ireland, Italy, Morocco, Qatar, Saudi Arabia, South Africa, Spain, United Kingdom, Bahamas, Barbados, Belize, Bermuda, Colombia, Dominican Republic, Ecuador, Guatemala, Honduras, Mexico, Panama, St. Thomas, Trinidad and Tobago.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports of Polyurethane Displacement in the dialyzer, and might be identified as a blood leak