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FDA (Device enforcement)Recalled 2024-04-18class ii

BD SWITZERLAND SARL: 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 produc

Hazard

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

Details from the source

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. 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. Quantity: 11.300 sets Lot/code info: Catalog Number: 10013072 UDI-DI code:07613203021210 Lot Number: 22115368

UPC codes

07613203021210

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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