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.
BD is recalling Alaris Pump Infusion Set Low Sorbing Tubing sets because the drip chamber can detach, potentially delaying treatment or exposing users to harsh fluids. This affects patients using the tubing for medical fluid delivery.
The tubing's drip chamber can become detached from the main tubing during use. This may cause delays in delivering critical medications or fluids, or expose users to harsh infusates that could cause irritation or injury.
Patients using the Alaris Pump Infusion Set with the specific tubing model are most at risk. Healthcare providers administering treatments with this tubing may also be affected.
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.
Identify the product by catalog number 10013072 or lot number 22115368 to confirm if it is affected.
The recall states the tubing may detach, causing treatment delays or exposure to harsh infusates. It is not safe to use without checking if it is affected.
Look for the catalog number 10013072 or lot number 22115368 on the tubing set.
The recall does not specify a remedy, so check with BD for guidance on safe handling or disposal.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-1944-2024 — BD BD Hello, I own a BD that is covered by recall Z-1944-2024 from BD. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
