BD SWITZERLAND SARL recalls
Every recall we track for BD SWITZERLAND SARL — 15 in all, from 2020–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from BD SWITZERLAND SARL more than tripled in 2025 (7, up from 1 in 2024).
All FDA recall records for BD SWITZERLAND SARL since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 2 | 0 | 3 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 1 | 0 | 0 | 1 |
| 2025 | 0 | 4 | 3 | 0 | 7 |
| 2026 (to date) | 0 | 1 | 3 | 0 | 4 |
What to do if you have a recalled BD SWITZERLAND SARL product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All BD SWITZERLAND SARL recalls
9 shown- Lower riskMedical device
BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,
BD recalls specific Alaris Pump Infusion Sets due to performance data discrepancies that may lead to inappropriate pump function. Affected models include various 0.2 micron filter and SmartSite Y-site sets. No remedy is provided in the recall notice.
BDAug 19, 2026 - Lower riskMedical device
BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site
BD recalls 60-inch non-DEHP minibore extension sets with UDI-DI codes 10885403236235, 10885403274619, and 10885403237218 due to potential inadequate sterilization processing.
BDJun 16, 2026 - Lower riskMedical device
BD SWITZERLAND SARL recalls MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering
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.
BDJun 4, 2026 - Use cautionMedical device
BD SWITZERLAND SARL recalls BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer
BD recalls Luer-Lok 360 stopcocks with UDI-DI code 00382903949106 due to potential overthreading causing unstable connections during IV fluid administration.
BDMay 21, 2026 - Lower riskMedical device
BD SWITZERLAND SARL recalls BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer
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.
BDJun 16, 2025 - Use cautionMedical device
BD SWITZERLAND SARL recalls BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500
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.
BDMay 12, 2025 - Lower riskMedical device
BD SWITZERLAND SARL recalls BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and
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.
BDFeb 20, 2025 - Use cautionMedical device
BD SWITZERLAND SARL recalls Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set
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.
BDApr 18, 2024 - Use cautionMedical device
BD SWITZERLAND SARL recalls BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identification Stripe ASV, Catalog Number 30893-07 -
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.
BDApr 9, 2020
BD SWITZERLAND SARL recall questions
How many recalls has BD SWITZERLAND SARL had?
15 recalls from BD SWITZERLAND SARL are on record with U.S. safety agencies, from 2020–2026.
What is the most recent BD SWITZERLAND SARL recall?
BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,, dated Aug 19, 2026. Every BD SWITZERLAND SARL recall is listed on this page, newest first.
What should I do if I have a recalled BD SWITZERLAND SARL product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new BD SWITZERLAND SARL recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.