FDA Device Recalls

Recalls / —

—#197272

Product

Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic and acute renal failure by hemodialysis.

FDA product code
KDI — Dialyzer, High Permeability With Or Without Sealed Dialysate System
Device class
Class 2
Medical specialty
Gastroenterology, Urology
510(k) numbers
K130039
Affected lot / code info
UDI-DI: 07332414124076; Product Code: 114746L; Lot Numbers: C421222601, C421222701, C421222801, C421222901, C421223001, C421223101, C421223201, C421223301, C421223401, C421223501, C421223601, C421223701, C421223801, C421223901, C421224001, C421224101, C421224201, C421224301, C421224401, C421224601, C421224701, C421224801, C421224901, C421225001, C421225101, C421225201, C421225301, C421225401, C421225501, C421225601, C421225701, C421225801, C421225901, C421226001, C421226101, C421226201, C421226301, C421226401, C421226501, C421226601, C421226701, C421226801, C421226901, C421227001, C421227101, C421227201, C421227301, C421227401, C421227501, C421227601, C421227701, C421227801, C421227901, C421228001, C421228101, C421228201, C421228301, C421228401, C421228501, C421228601, C421228701, C421228801, C421228901, C421229001, C421229101, C421229201, C421229301, C421229401, C421231001, C421240001, C421240101, C421240201, C421240301, C421240401, C421240501, C421240601, C421240701, C421240801, C421240901, C421241001, C421241101, C421241201, C421241301, C421241401, C421241501, C421241601, C421241701, C421241801, C421241901, C421242001, C421242101, C421242201, C421242301, C421242401, C421242501, C421242601, C421242801, C422200101, C422200201, C422200301, C422200501, C422200601, C422200701, C422200801, C422200901, C422201001, C422201101, C422201201, C422201701, C422201801, C422202101, C422202201, C422202301, C422205001, C422205101, C422205201, C422205301, C422205701, C422205801, C422205901, C422206001, C422206101, C422206201, C422206301, C422206401, C422206501, C422206601, C422206701, C422206801, C422206901, C422207001, C422207201, C422207301, C422207401, C422207501, C422207601, C422207701, C422207801, C422207901, C422208001, C422208101, C422208201, C422208301, C422208401, C422208501, C422208601, C422208701, C422208801, C422208901, C422209001, C422209101, C422209201, C422209301, C422209401, C422209501, C422209801, C422209901, C422210001, C422210101, C422210201, C422210301, C422210401, C422210501, C422210601, C422210701, C422211201, C422211301, C422211401, C422211501, C422211601, C422211701, C422211801, C422211901, C422212001, C422212101, C422212201, C422212301, C422212401, C422212501, C422212601

Why it was recalled

Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer

Root cause (FDA determination)

Process change control

Action the firm took

Baxter Healthcare sent a notification via USPS first class mail on about 11/23/2022 and to home patients on about 11/29/2022. Consignees were instructed to locate and remove all affected product from your inventory, contact Baxter Healthcare Center for Service to arrange for return and credit, and acknowledge the receipt of the notification by completing a reply form on the customer portal. Note: this letter describes two issues. This recall addresses Internal Blood Leaks being caused by a twisted gasket in the dialyzer. The second issue is linked to reports of Polyurethane Displacement in the dialyzer, which is addressed in a separate recall.

Recalling firm

Firm
Baxter Healthcare Corporation
Address
1 Baxter Pkwy, Deerfield, Illinois 60015-4625

Distribution

Distribution pattern
Worldwide distribution. US Nationwide including Guam and St. Thomas USVI; 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, and Trinidad and Tobago.

Timeline

Recall initiated
2022-11-23
Posted by FDA
2022-12-22
Status
—

Source: openFDA Device Recall endpoint. Recall record ID #197272. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.