BD SWITZERLAND SARL: Medical Device Recall in 2024 - (Recall #: Z-1944-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood products.

Product Classification:

Class II

Date Initiated: April 18, 2024

Date Posted: June 12, 2024

Recall Number: Z-1944-2024

Event ID: 94479

Reason for Recall:

Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.

Status: Ongoing

Product Quantity: 11.300 sets

Code Information:

Catalog Number: 10013072 UDI-DI code:07613203021210 Lot Number: 22115368

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated