Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 00085412007731, Lot/Serial Numbers: H23J16074, H23K01082, H23K06107, H23K09093, H23K28051, H23K30081, H23L07053, H23L13051, H23L27093, H24A03061, H24A09035, H24A11064, H24A29132, H24B02038, H24B12086, H24B21079, H24B28090, H24B29072, H24B29098, H24C21093, H24C27090, H24D08064, H24D11050, H24D17040, H24D22081, H24D26058, H24D30076, H24E06065, H24E23037, H24E28051, H24F03045, H24F05065, H24F17086, H24F24033, H24F27036, H24H05061, H24H08032, H24H13040, H24H16043, H24H22025
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Baxter Healthcare Corporation
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Product Codes/Lot Numbers:
UDI/DI 00085412007731, Lot/Serial Numbers: H23J16074, H23K01082, H23K06107, H23K09093, H23K28051, H23K30081, H23L07053, H23L13051, H23L27093, H24A03061, H24A09035, H24A11064, H24A29132, H24B02038, H24B12086, H24B21079, H24B28090, H24B29072, H24B29098, H24C21093, H24C27090, H24D08064, H24D11050, H24D17040, H24D22081, H24D26058, H24D30076, H24E06065, H24E23037, H24E28051, H24F03045, H24F05065, H24F17086, H24F24033, H24F27036, H24H05061, H24H08032, H24H13040, H24H16043, H24H22025
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0559-2025
Related Recalls
Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff.
Baxter Healthcare
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.
CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve, 10 drops/mL, 92-inch (2.3 meters), Product code 2C8419
Baxter Healthcare
IV sets may leak.