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Displaying 1 - 4 of 4 items.
Baxter Corporation is issuing an urgent medical device correction due to a defect in the Dose IQ Safety Software used with Novum IQ Large Volume Pump, resulting in an invalid initial setting for the air-in-line threshold for any new care area created in…
RecallHealth product recall | 2023-06-07
Baxter Corporation is issuing an urgent medical device recall for all non-expired lots of Self-Righting Luer Slip And Luer Lock Tip Caps listed due to the potential of the packaging seal not maintaining a sterile barrier for the tip caps.
Recall start…
RecallHealth product recall | 2022-08-02
Baxter Corporation is issuing a correction for the Prismax. If the operator initiates therapy by entering a value other than the default value for the patient gain/loss limit or the return pressure drop limit and uses the same patient function, the…
RecallHealth product recall | 2022-03-29
Baxter Corporation has received one complaint of a customer getting self-righting luer lock tip caps, yellow (product code h938690025) mislabeled as self-righting luer slip tip caps, yellow (product code h93866100).
Recall start date: Feb 28, 2022
RecallHealth product recall | 2022-03-14