REVACLEAR 300 Dialyzer, Product Code 114745L Revaclear 300 and Revaclear 400 dialyzers are indicated for treatment of chronic and acute renal failure by hemodialysis.
FDA Recall Z-1908-2019 · Posted None
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Recalling FirmBaxter Healthcare Corporation
Recall StatusTerminated
Product CodeKDI
Date Initiated2019-05-31
Date Terminated2020-10-05
Product Quantity1249272 units
Reason for Recall
There is a potential presence of ruptured dialyzer fibers which may lead to a blood leak during treatment.
Firm Action
The firm, Baxter, sent an " Urgent Product Recall" letter on 05/31/2019. The notice described the product, problem and actions to be taken. The customers were instructed to do the following:
1. Locate and remove all affected product lots from your facility. The product code and lot number can be found on the individual product or shipping carton.
2. Contact Baxter Healthcare Center for Service to arrange for return and credit.
Baxter Healthcare Center for Service can be reached at 888-229-0001 between
the hours of 7:00 am and 6:00 pm Central Time, Monday through Friday. Please
have your Baxter 8-digit ship-to account number, product code, lot number, and
quantity of product to be returned ready when calling.
3. If you purchased this product directly from Baxter, complete the enclosed
Baxter customer reply form and return it to Baxter by faxing it to 224-270-5457 or scanning and e-mailing it to [email protected], even if you do not have any inventory. Returning the customer reply form promptly will confirmyour receipt of this notification and prevent you from receiving repeat notices.
4. If you purchased this product from a distributor, please note that the Baxter
customer reply form is not applicable. If a reply form is provided by your distributor or wholesaler, please return it to the supplier according to their instructions.
5. If you distribute this product to other facilities or departments within your institution, please forward a copy of this communication to them.
6. If you are a dealer, wholesaler, distributor/reseller, or original equipment
manufacturer (OEM) that distributed any affected product to other facilities, please conduct a consumer-level recall of the affected product that you distributed to customers.
For general questions regarding this communication, contact Baxter Corporate
Product Surveillance at 800-437-5176, between the hours of 8:00 am and 5:00 pm Central Time, Monday through Friday.
.
Root Cause
Process control
Distribution Pattern
US Nationwide Distribution and Internationally to: Canada and Bermuda.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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