United StatesBD Switzerland Sarl is recalling specific intravascular administration and extension sets: 60 In Non-DEHP Minibore Extension Set RES ME2010 (UDI‑DI 10885403236235, Lot 26025260), MaxPlus Extension Set w/ Needleless and Y‑Site REF MPX5305‑C (UDI‑DI 10885403274619, Lot 26035455), and 9 In Extension Set w/ Max Y REF MPX5300‑C (UDI‑DI 10885403237218, Lot 26055528). The products are being recalled because they may not have received adequate sterilization processing.
What's being recalled
60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Intravascular Administration Set and Extension Set used to administer fluids.
Recalling firm: BD Switzerland Sarl, Eysins, Switzerland.
How to identify it
60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 Lot Number: 26025260 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 Lot Number: 26035455 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Lot Number: 26055528
The hazard
Products may not have received adequate sterilization processing.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
U.S.: AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MO, MS, NC, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA O.U.S.: Canada
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)
Canada