Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 49–60 of 81 recalls
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.
There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
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.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket.…
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.