# FDA recall Z-3080-2026

> **BD SWITZERLAND SARL** · Class I · device recall initiated 2026-08-19.

## Product

BD Alaris Pump Infusion Sets 10561554*	10885403232565	50885403232563	BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 SmartSite Y-sites 10015861A	10885403232626	50885403232624	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing, Back Check Valve, 3 SmartSite Y-sites 11171447*	7613203021234	37613203021242	BD Alaris Pump Infusion Set, 2 Back Check Valves, 3 SmartSite Y-sites 11426965*	10885403232558	50885403232556	BD Alaris Pump Infusion Set, Back Check Valve, 5 SmartSite Y-sites 2260-0500	7613203012591	37613203012608	BD Alaris Pump Infusion Set, PE Lined Tubing 24600-0007	10885403241970	50885403241978	BD Alaris Pump Infusion Set, PE Lined Tubing, Back Check Valve, 3 SmartSite Y-sites 2278-0500	10885403223266	50885403223264	BD Alaris Pump Infusion Blood Set, 200 Micron Filter 2477-0007	7613203019460	37613203019478	BD Alaris Pump Infusion Blood Set, 180 Micron Filter, SmartSite Y-site 22603-B007T	10885403240942	50885403240940	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing, Bonded Texium Closed Male Luer with Priming Cap 24010-0007T	10885403271021	50885403271029	BD Alaris Pump Infusion Set, Bonded Texium, Closed Male Luer with Priming Cap, Back Check Valve, 3 SmartSite Y-sites 24301-0007T	10885403223198	50885403223196	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, 0.2 Micron Filter, PE Lined Tubing, Bonded Texium Closed Male Luer with Priming Cap, SmartSite Y-site 24601-B007T	10885403240959	50885403240957	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing, Bonded Texium Closed Male Luer with Priming Cap, Back Check Valve, 2 SmartSite Y- sites 22602-B007T	10885403240935	50885403240933	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing, Bonded Texium Closed Male Luer with Priming Cap 11426964	10885403232367	50885403232365	BD Alaris¿LVP 20D LOW SORB 2204-0007*	10885403199363	50885403199361	BD Alaris Pump Infusion Set 10015862	10885403221866	50885403221864	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing 10010453	7613203021135	37613203021143	BD Alaris Pump Infusion Set, 1.2 Micron Filter, PE Lined Tubing, SmartSite Y-site 11532269	10885403232343	50885403232341	BD Alaris Pump Infusion Set, 0.2 Micron Filter, Back Check Valve, PE Lined Tubing, 2 SmartSite Y-sites 2202-0007*	10885403274039	50885403274037	BD Alaris Pump Infusion Set, 1.2 Micron Filter 2432-0007*	10885403232329	50885403232327	BD Alaris Pump Infusion Set, 0.2 Micron Filter, Back Check Valve, 3 SmartSite Y-sites 10010454	7613203015806	37613203015814	BD Alaris Pump Infusion Set, 0.2 Micron Filter, PE Lined Tubing, SmartSite Y-site 2465-0007	10885403221941	50885403221949	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, 0.2 Micron Filter, PE Lined Tubing, SmartSite Y-site 10015012	10885403233951	50885403233959	BD Alaris Pump Infusion Burette Set, 0.2 Micron Filter, Smallbore Tubing, SmartSite Port (Burette), SmartSite Y-site 2441-0007	10885403235047	50885403235045	BD Alaris Pump Infusion Burette Set, Smallbore Tubing, SmartSite Port (Burette), 3 SmartSite Y-sites 11419365	10885403234736	50885403234734	BD Alaris Pump Infusion Set, Back Check Valve, Manifold, 3-Way Stopcock, 5 SmartSite Y-sites 2423-0007	7613203020985	37613203020979	BD Alaris Pump Infusion Set, Back Check Valve, 2 Ganged 4-Way Stopcocks, 4 SmartSite Y-sites 10813621	10885403234514	50885403234512	BD Alaris Pump Infusion Set, Back Check Valve, 3 Ganged 4-Way Stopcocks, 4 SmartSite Y-sites 10010483	10885403232602	50885403232600	BD Alaris Pump Infusion Set, Vented Syringe Adapter, Smallbore Tubing 10013072	7613203021210	37613203021228	BD Alaris Pump Infusion Set, PE Lined Tubing, Back Check Valve, 2 SmartSite Y-sites 10013361	10885403221965	50885403221963	BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, Back Check Valve, 2 SmartSite Y-sites 10013890	10885403232268	50885403232266	BD Alaris Pump Infusion Set, PE Lined Tubin

## Reason for recall

Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.

## Distribution

U.S.: Nation-wide - AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY.  O.U.S.:  Australia Belgium Bahrain Botswana Canada Cuba China France Germany Gibraltar Israel India Italy Japan Korea, Republic of Kuwait Mexico Malaysia Netherlands New Zealand Philippines Pakistan Qatar Saudi Arabia Singapore South Africa Switzerland Taiwan, Province of China Turkey United Arab Emirates United Kingdom

## Key facts

- **Recall number:** Z-3080-2026
- **Recalling firm:** BD SWITZERLAND SARL
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-08-19
- **Report date:** 2026-09-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Eysins, N/A, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3080-2026

## Citation

> MORVS. FDA recall Z-3080-2026. Retrieved 2026-10-25 from https://api.morvs.ai/recall/Z-3080-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*