Fresh Recalls

BD SWITZERLAND SARL recalls

4 recent recalls on record for BD SWITZERLAND SARL in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code (1)BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusi (1)BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code (1)MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number (1)

All BD SWITZERLAND SARL recalls

FDA Class I · Medical device · September 23, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusi recall — BD SWITZERLAND SARL

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

Official ID Z-3080-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall — BD SWITZERLAND SARL

Products may not have received adequate sterilization processing.

Official ID Z-2941-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number recall — BD SWITZERLAND SARL

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

Official ID Z-2654-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code recall — BD SWITZERLAND SARL

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 …

Official ID Z-2514-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.