BD Switzerland Sarl recalls

BD Switzerland Sarl has 15 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 23 Sep 2026. 12 are still ongoing. 4 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls15since 2020

Last 12 months4reported

Class I17% of total

Ongoing12latest 23 Sep 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 1 0May 5 0 0Aug 1 0 0Nov 0 0 0Feb 0 0 0May 1 1 1Aug 1 0

Severity split

Class I 1 7%Class II 14 93%Class III 0 0%

Why bd switzerland sarl is recalled

Product types

By year

2026427%
2025747%
202417%
2020320%

Ongoing bd switzerland sarl recalls

12 active

Reported	Class	Recall	Company	Reason	Where
23 Sep 2026Device	CLASS I	BD Alaris Pump Infusion Sets 10561554* recalled by BD Switzerland Sarl	BD Switzerland Sarl	Other	Nationwide
19 Aug 2026Device	CLASS II	Non-DEHP Minibore Extension Set RES ME2010 recalled	BD Switzerland Sarl	Sterility	26 states
8 Jul 2026Device	CLASS II	Medline 111 Gravity Set W/3 Needle Free Y-Sites recalled	BD Switzerland Sarl	Other	IL
24 Jun 2026Device	CLASS II	BD Connecta" BD Luer-Lok" recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Foreign Material	39 states
3 Sep 2025Device	CLASS II	BD PhaSeal Injector Luer (N30C) recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Packaging Defects	Nationwide
18 Jun 2025Device	CLASS II	BD Texium recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Sterility	Nationwide

All bd switzerland sarl recalls, newest first

15 total

Reported	Class	Recall	Company	Reason	Where
23 Sep 2026Device	CLASS I	BD Alaris Pump Infusion Sets 10561554* recalled by BD Switzerland Sarl	BD Switzerland Sarl	Other	Nationwide
19 Aug 2026Device	CLASS II	Non-DEHP Minibore Extension Set RES ME2010 recalled	BD Switzerland Sarl	Sterility	26 states
8 Jul 2026Device	CLASS II	Medline 111 Gravity Set W/3 Needle Free Y-Sites recalled	BD Switzerland Sarl	Other	IL
24 Jun 2026Device	CLASS II	BD Connecta" BD Luer-Lok" recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Foreign Material	39 states
3 Sep 2025Device	CLASS II	BD PhaSeal Injector Luer (N30C) recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Packaging Defects	Nationwide
18 Jun 2025Device	CLASS II	BD Texium recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Sterility	Nationwide
18 Jun 2025Device	CLASS II	Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented recalled	BD Switzerland Sarl	Sterility	Nationwide
18 Jun 2025Device	CLASS II	Bd Texium Closed Male Luer With Female Cap recalled	BD Switzerland Sarl	Sterility	Nationwide
18 Jun 2025Device	CLASS II	BD Texium Needle-Free Syringe recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Sterility	Nationwide
18 Jun 2025Device	CLASS II	Bd Texium Closed Male Luer With Female Cap recalled	BD Switzerland Sarl	Sterility	Nationwide
9 Apr 2025Device	CLASS II	BD Connecta BD Luer-Lok recalled by Bd Switzerland Sarl	BD Switzerland Sarl	Other	35 states
12 Jun 2024Device	CLASS II	Alaris Pump Infusion Set Low Sorbing Tubing recalled	BD Switzerland Sarl	Other	Nationwide
20 May 2020Device	CLASS II	BD Alaris PCEA Administration Set, Microbore Tubing recalled	BD Switzerland Sarl	Packaging Defects	Nationwide
20 May 2020Device	CLASS II	BD Alaris PCEA Administration Set, Microbore Tubing recalled	BD Switzerland Sarl	Packaging Defects	Nationwide
20 May 2020Device	CLASS II	BD Alaris PCEA Administration Set, Microbore Tubing recalled	BD Switzerland Sarl	Packaging Defects	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.