Use cautionMedical device recall · FDA · Published April 18, 2024
BD Alaris Pump Infusion Set: Risk of Treatment Delays from Detached Tubing
BD recalls Alaris Pump Infusion Set Low Sorbing Tub: tubing may detach causing treatment delays or exposure to harsh infusates. Check product details to see if affected.
Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.
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Contact the company
📍Recalling firmBD SWITZERLAND SARLTerre Bonne Park A4, Route De Crassier 17 · Eysins, Switzerland
“BD Alaris Pump Infusion Set: Risk of Treatment Delays from Detached Tubing.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/55343-bd-alaris-pump-infusion-set-risk-of-treatment-delays-from. Based on FDA recall #Z-1944-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1944-2024%22&limit=1).
BD SWITZERLAND SARL recalled Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 tubing sets on April 18, 2024, according to the FDA. The drip chamber may detach from the tubing, potentially causing treatment delays or exposing users to harsh infusates.
How to tell if you have it
Brand: BD
Product: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites
REF: 10013072
Catalog Number: 10013072
UDI-DI code: 07613203021210
Lot Number: 22115368
Quantity: 11,300 sets
The hazard
The recall involves the infusion set tubing drip chamber becoming detached from the tubing. This defect may cause delays in treatment or unintentionally expose users to harsh infusates.
Context
GovInfoNow's records show BD SWITZERLAND SARL has issued eight other recalls since April 9, 2020. Other recent recalls of similar products include BD Alaris Pump Infusion Sets Recall: Performance Data Discrepancies May Cause Inappropriate Pump Function (Aug. 19, 2026), BD 60-In Extension Sets: Risk of Inadequate Sterilization (June 16, 2026), and BD MEDLINE 111 Gravity Set with 3 Needle-Free Y-Sites: Not for Human Use Hazard (June 4, 2026). Other recent recalls of similar products include BD Alaris Infusion Pump Module 8100 Recall: Drop or Jar Risk (Oct. 17, 2025), Fresenius Medical Care 5008X Blood Tubing Set Recall: Risk of Blood Leak During Treatment (Aug. 10, 2026), and B Braun SAFELINE IV Sets: Risk of Medication Backflow and Occlusion (Oct. 29, 2025).
How to tell if you have this one
Check for the product name: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites. The catalog number is 10013072. This tubing was sold with the lot number 22115368.
Brand
BD
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify the product by catalog number 10013072 or lot number 22115368 to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 13 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of AR, CA, CO, IL, KS, MA, ME, NJ, NY, PA, SD, WA and WI. The country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arkansas, California, Colorado, Illinois, Kansas, Maine, Massachusetts, New Jersey, New York, Pennsylvania, South Dakota, Washington, Wisconsin.
Recall timeline
FDA published this recall 55 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1944-2024 (April 18, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1944-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.