Bd Switzerland Sarl recalls
8 official recalls and safety alerts involving Bd Switzerland Sarl since 2024-06, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Bd Switzerland Sarl or the relevant agency.
- 2026-09-23
USBD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3…
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.
FDA · DeviceBD SWITZERLAND SARLU.S.: Nation-wide - AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA,…Official notice →- 2026-08-19
- US
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 REF MPX5305-C UDI-DI…
Products may not have received adequate sterilization processing.
FDA · DeviceBD SWITZERLAND SARLU.S.: AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MO, MS, NC, NV, NY, OH, OK,…Official notice → - 2026-07-08
- US
BD SWITZERLAND SARL recalls MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Sample/Not for Human Use
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
- 2026-06-24
- US
BD SWITZERLAND SARL recalls BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication…
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 led some clinical users to perceive…
FDA · DeviceBD SWITZERLAND SARLU.S.: AK, AL, AR, AZ, CA, CO, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI,…Official notice → - 2025-09-03
- US
BD SWITZERLAND SARL recalls BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF:…
Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it.
FDA · DeviceBD SWITZERLAND SARLUS Nationwide distribution including in the states of CA, WA, AL, OH, NC, GA,…Official notice → - 2025-06-18
- US
BD SWITZERLAND SARL recalls BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500
Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may…
FDA · DeviceBD SWITZERLAND SARLWorldwide - US Nationwide distribution including in the states of MA, CA, IL,…Official notice → - 2025-04-09
- US
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 3-way Stopcocks are…
Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU)
FDA · DeviceBD SWITZERLAND SARLU.S.: AK, AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO,…Official notice → - 2024-06-12
- US
BD SWITZERLAND SARL recalls Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of…
Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.
FDA · DeviceBD SWITZERLAND SARLWorldwide - US Nationwide distribution in the states of AR, CA, CO, IL, KS,…Official notice →