BD SWITZERLAND SARL Recalls

4 recalls on record in the United States

medical: 4
medical Class II
2026-06-24

BD SWITZERLAND SARL recalls BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382

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 securely. This behavior has led some clinical users to perceive the connection as unstable.

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medical Class II
2026-07-08

BD SWITZERLAND SARL recalls MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0

Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.

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medical Class II
2026-08-19

BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI cod

Products may not have received adequate sterilization processing.

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medical Class I
2026-09-23

BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 508854

Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.

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