Baxter Healthcare Corporation MiniCap Extended Life PD Transfer Set Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MiniCap Extended Life PD Transfer Set
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
Product Code: 5C4482, UDI: 00085412007731, Lot#, Expiration Date: H20D13100, 4/13/2025, H20D27084, 4/27/2025, H20D30070, 4/30/2025, H20E13107, 5/13/2025, H20E19054, 5/19/2025, H20E22082, 5/22/2025, H20F09061, 6/9/2025, H20F15050, 6/15/2025, H20F18070, 6/18/2025, H20F24086, 6/24/2025, H20F29051, 6/29/2025, H20G13046, 7/13/2025, H20G27087, 7/27/2025, H20G30065, 7/30/2025, H20H05057, 8/5/2025, H20H14067, 8/14/2025, H20H19066, 8/19/2025
Products Sold
Product Code: 5C4482, UDI: 00085412007731, Lot#, Expiration Date: H20D13100, 4/13/2025; H20D27084, 4/27/2025; H20D30070, 4/30/2025; H20E13107, 5/13/2025; H20E19054, 5/19/2025; H20E22082, 5/22/2025; H20F09061, 6/9/2025; H20F15050, 6/15/2025; H20F18070, 6/18/2025; H20F24086, 6/24/2025; H20F29051, 6/29/2025; H20G13046, 7/13/2025; H20G27087, 7/27/2025; H20G30065, 7/30/2025; H20H05057, 8/5/2025; H20H14067, 8/14/2025; H20H19066, 8/19/2025
Baxter Healthcare Corporation is recalling MiniCap Extended Life PD Transfer Set due to Potential for no-flow and leaks under the twist clamp.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for no-flow and leaks under the twist clamp.
Recommended Action
Per FDA guidance
Urgent Medical Device Recall FA-2020-055 was sent to Peritoneal Dialysis Centers via U.S.P.S., first class mail on November 10, 2020. Urgent Medical Device Recall FA-2020-055 was sent via U.S.P.S., first class mail on November 13, 2020 to Home Patients who received impacted lots directly from Baxter. Out of an abundance of caution, Baxter will also be mailing the communication to all home patients who receive treatment at Peritoneal Dialysis Centers which received the impacted lots of transfer sets, regardless if the patient received the set or not.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026