Every recall we track for BD SWITZERLAND SARL — 14 in all — plus the complaints and injury reports the public filed about them.
BD recalls 60-inch non-DEHP minibore extension sets with UDI-DI codes 10885403236235, 10885403274619, and 10885403237218 due to potential inadequate sterilization processing.
BD recalls MEDLINE 111 Gravity Set with 3 Needle-Free Y-Sites (Catalog SAM2461) shipped as engineering sample labeled 'Not for Human Use' in the U.S. market.
BD recalls Luer-Lok 360 stopcocks with UDI-DI code 00382903949106 due to potential overthreading causing unstable connections during IV fluid administration.
BD recalls several PhaSeal injector luer devices sold in the U.S. due to missing U.S. instructions for healthcare professionals. This could lead to review issues if prompted. Affected products include specific models with reference numbers.
BD recalls 3mL-60mL Texium syringes with specific reference numbers due to potential leaks at the needle-free connector interface, risking medication underdosing or exposure to hazardous drugs.
BD recalls Alaris Pump Infusion Sets with SmartSite bags that may leak at connections, risking treatment delays or medication underdosing. Check product references listed.
BD recalls closed male luer connectors that may leak at the interface with needle-free connectors, causing treatment interruptions or medication underdosing. Affected units include specific model numbers and dates.
BD recalls specific needle-free syringes (3mL to 60mL) due to potential leaks at the connection point, which could cause treatment delays, medication underdosing, or exposure to hazardous drugs.
BD recalls certain Texium closed male luer with female cap connectors due to potential leaks at the interface, which could cause treatment interruptions, medication underdosing, or exposure to hazardous drugs.
BD recalls Connecta Luer-Lok 360 and Plus models with specific lot numbers due to outside US instructions that could lead to IV therapy errors.
BD recalls Alaris Pump Infusion Set Low Sorbing Tub: tubing may detach causing treatment delays or exposure to harsh infusates. Check product details to see if affected.
BD recalls Alaris PCEA Administration Sets with yellow tubing that may leak, causing under-infusion of medication and inadequate pain control. Affected units have specific catalog numbers and lot numbers.
BD recalls microbore tubing with yellow stripe for potential leaks causing under-infusion of medication and inadequate pain control during use.
BD recalls Alaris PCEA Administration Sets with yellow tubing that may leak, causing under-infusion of medication and inadequate pain control. Affected units have specific catalog numbers and lot ranges.
