FDAFDA · Food and drugs·Recall number Z-0569-2025
Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialysis
Published December 4, 2024 · Recall initiated: October 23, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- Worldwide distribution.
- Lot
- UDI/DI 0085412150703, Lot/Serial Numbers: H23J02025, H23L04043, H23L05057, H23L05073, H24A29041, H24C01061, H24E13061, H24G15062
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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