Reported Jun 18, 2025 · Ongoing
Alaris Pump Infusion Set
Bd Switzerland Sarl
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: BD SWITZERLAND SARL · Terre Bonne Park A4 · Eysins · N/A
Is this the product you have?
Alaris Pump Infusion Set
15 products · 330 lot codes
10013361TSmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite Y-Sites
- UDI-DI
10885403223204
28 recalled lot codes
23025303February 102026)23035235March 112026)23045223April 62026)23075395July 172026)23085227August 82026)23115150November 82026)23115151November 82026)23125167December 52026)24025684February 62027)24045377April 232027)24055576May 272027)24075224July 262027)24105079October 112027)24115159November 72027)
10321213TSmartSite Bag Access Non-Vented Bonded Texium Closed Male Luer With Priming Cap
- UDI-DI
10885403228971
12 recalled lot codes
23035169March 152026)23045174April 42026)23085140August 32026)23095142September 112026)23105297October 122026)24025686February 62027)
22000-B007TSmartSite Bag Access Non-Vented Low Sorbing Tubing (PE Lined) Bonded Texium Closed Male Luer With Priming Cap
- UDI-DI
10885403245022
22 recalled lot codes
23025320February 132026)23045224April 112026)23065209June 102026)23075394July 212026)23095143September 112026)23105133October 62026)24015278January 132027)24025685February 62027)24036209March 252027)24075260July 262027)24066653June 242027)
22600-0007TLow Sorbing Tubing (PE Lined) Bonded TexiumTM with priming cap
- UDI-DI
10885403239595
6 recalled lot codes
23095151September 112026)24036205March 252027)24055601May 272027)
Page 1 of 4
- Amount recalled
- 2,024,780
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
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 cause procedure delay, treatment interruptions, exposure to hazardous drugs, and/or underdosing of medication.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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