BD SWITZERLAND SARL recalls

4 recalls.

• BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump... recall (BD SWITZERLAND SARL)
  Medical deviceClass IReported September 23, 2026 · Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.
• 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 ... recall (BD SWITZERLAND SARL)
  Medical deviceClass IIReported August 19, 2026 · Products may not have received adequate sterilization processing.
• MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number:... recall (BD SWITZERLAND SARL)
  Medical deviceClass IIReported July 8, 2026 · Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
• BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta"... recall (BD SWITZERLAND SARL)
  Medical deviceClass IIReported June 24, 2026 · Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening...