60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall
BD SWITZERLAND SARL recalled 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code on August 19, 2026 because of products may not have received adequate sterilization processing. It was sold in 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.
Why it was recalled
Products may not have received adequate sterilization processing.
What's 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.
Quantity: 93,700
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- BD SWITZERLAND SARL, Eysins
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- 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
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 - Status
- Ongoing
- Recall number
- Z-2941-2026
- Source
- U.S. Food and Drug Administration
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