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U.S. Department of Health and Human Services

Class 2 Device Recall Revaclear

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 Class 2 Device Recall Revaclearsee related information
Date Initiated by FirmNovember 23, 2022
Date PostedDecember 22, 2022
Recall Status1 Open3, Classified
Recall NumberZ-0762-2023
Recall Event ID 91223
510(K)NumberK130039 
Product Classification Dialyzer, high permeability with or without sealed dialysate system - Product Code KDI
ProductRevaclear 300 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
Code Information UDI-DI: 07332414123055; Product Code: 114745L; All lot numbers from C419128801-C422128401
Recalling Firm/
Manufacturer
Baxter Healthcare Corporation
1 Baxter Pkwy
Deerfield IL 60015-4625
For Additional Information ContactCenter for One Baxter
800-422-9837
Manufacturer Reason
for Recall
Reports of Polyurethane Displacement in the dialyzer, and might be identified as a blood leak
FDA Determined
Cause 2
Process control
ActionBaxter Healthcare notified healthcare facilities on 11/23/2022 and home patients on 11/29/2022, via first class mail. Consignees were instructed to be aware of the difference in appearances between Polyurethane Displacement and an Internal Blood Leak and ensure staff is also aware. Additionally, consignees were instructed that if there is a blood leak alarm, to follow your clinical practice to stop treatment, and if only the Polyurethane Displacement is observed, to continue use of the dialyzer. Consignees were asked to acknowledge receipt of the notification by completing and returning the response form.
Quantity in Commerce14,053,824 units
DistributionWorldwide 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.
Total Product Life CycleTPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = KDI
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