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Bd Switzerland Sarl

Complete recall history across all FDA and CPSC categories — 11 total recalls

Bd Switzerland Sarl appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (11)

FDA medical device enforcement actions by Bd Switzerland Sarl

Date Product Reason Class
Jun 16, 2025 BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (... Closed system drug transfer devices were shipped to the U.S. market without a... Class II
May 12, 2025 BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010... Sterile, single use closed system drug transfer devices, standalone or on inf... Class II
May 12, 2025 Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With... Sterile, single use closed system drug transfer devices, standalone or on inf... Class II
May 12, 2025 BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241; BD TEXIUM (China)... Sterile, single use closed system drug transfer devices, standalone or on inf... Class II
May 12, 2025 BD Texium Needle-Free Syringe: 3 mL, REF: MY8003; 5 mL, REF: MY8005; 10 mL, R... Sterile, single use closed system drug transfer devices, standalone or on inf... Class II
May 12, 2025 BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500 Sterile, single use closed system drug transfer devices, standalone or on inf... Class II
Feb 20, 2025 BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Conne... Due to specific lots of luer-lok devices were shipped to the U.S. market with... Class II
Apr 18, 2024 Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 Sma... Due to infusion set tubing drip chamber becoming detached from the tubing pot... Class II
Apr 9, 2020 BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identificatio... The products have the potential to leak between the connection of the male lu... Class II
Apr 9, 2020 BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identificatio... The products have the potential to leak between the connection of the male lu... Class II
Apr 9, 2020 BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identificatio... The products have the potential to leak between the connection of the male lu... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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