Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.
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
07613203021210
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.