FDAClass IIDecember 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist recall

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

Why was Baxter MiniCap Extended Life PD Transfer Set with Twist recalled?

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 04987456422890, Lot/Serial Numbers: H23L06097, H24A29033

Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis
Recalling firm
Baxter Healthcare Corporation
Quantity
1496 units
Distribution
Worldwide distribution.
Recall date
December 4, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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