Overview of recall records associated with Baxter Healthcare Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 260, Class I: 60, Class III: 8.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to…
The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
This page summarizes recall records in which the official source identifies Baxter Healthcare Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
