Bd Switzerland Sarl recalls
Bd Switzerland Sarl has 14 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 19 Aug 2026. 11 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is sterility.
Total recalls14since 2020
Last 12 months3reported
Class I00% of total
Ongoing11latest 19 Aug 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 14 100%Class III 0 0%
Why bd switzerland sarl is recalled
Product types
By year
Ongoing bd switzerland sarl recalls
11 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Non-DEHP Minibore Extension Set RES ME2010 recalled | Bd Switzerland Sarl | Sterility | 26 states |
| Device | CLASS II | Medline 111 Gravity Set W/3 Needle Free Y-Sites recalled | Bd Switzerland Sarl | Other | IL |
| Device | CLASS II | BD Connecta" BD Luer-Lok" recalled by Bd Switzerland Sarl | Bd Switzerland Sarl | Foreign Material | 39 states |
| Device | CLASS II | BD PhaSeal Injector Luer (N30C) recalled by Bd Switzerland Sarl | Bd Switzerland Sarl | Packaging Defects | Nationwide |
| Device | CLASS II | BD Texium recalled by Bd Switzerland Sarl | Bd Switzerland Sarl | Sterility | Nationwide |
| Device | CLASS II | Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented recalled | Bd Switzerland Sarl | Sterility | Nationwide |
All bd switzerland sarl recalls, newest first
14 totalAbout 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.