Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwitzerlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Becton DickinsonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list BD Switzerland Sàrl with 15 device recalls. The most recent is a device recall dated Aug 19, 2026: BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infu….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 19, 2026 | BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 SmarClass I · Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate p | Device recalls |
| Jun 16, 2026 | 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-DClass II · Products may not have received adequate sterilization processing. | Device recalls |
| Jun 4, 2026 | MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Sample/Not for Human Class II · Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market. | Device recalls |
| May 21, 2026 | BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication Class II · Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue | Device recalls |
| Jun 16, 2025 | BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF: 5Class II · Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, | Device recalls |
| May 12, 2025 | BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500Class II · Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at | Device recalls |
| May 12, 2025 | BD Texium Needle-Free Syringe: 3 mL, REF: MY8003; 5 mL, REF: MY8005; 10 mL, REF: MY8010; 20 mL, REF: MY8020; 30 mL, REF: MY8030; 60 mL, REF:Class II · Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at | Device recalls |
| May 12, 2025 | BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241; BD TEXIUM (China), REF: 10012241 CHINAClass II · Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
