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Displaying 1 - 15 of 387 items.
Affected lot may contain the presence of glass particulate.
RecallHealth product recall | 2023-09-20
Epiphany, now a Baxter Healthcare company, is issuing an urgent medical device correction for the Cardio Server E3 ECG Management System Software due to a report of the caliper tool becoming non-responsive, preventing the caliper function from being used…
RecallHealth product recall | 2023-09-07
Affected lot may result in a false negative for skin test (pecan nut allergy)
RecallHealth product recall | 2023-09-07
The pumps have the potential for the upstream occlusion sensor to cease proper function due to the build-up of electrostatic charge during operation triggering false downstream and upstream occlusion alarms.
Recall Start Date: August 28, 2023
RecallHealth product recall | 2023-09-07
Cardinal Health Canada has been notified of an urgent product recall initiated by Ecolab for the equipment drapes, table cover, and surgical room turnover (SRT) kits. Ecolab as Microtek has received odor complaints on certain lots. The odor has been…
RecallHealth product recall | 2023-08-24
Affected lots may contain the undeclared ingredients sildenafil and tadalafil.
RecallHealth product recall | 2023-08-23
Affected lots may contain the undeclared ingredient sildenafil.
RecallHealth product recall | 2023-08-22
Hamilton Medical Ag is recalling certain of the ventilators' Hamilton-C1/T1/mr1 control boards after receiving reports that the device may interrupt ventilation due to a faulty capacitor.
Recall start date: August 1, 2023
RecallHealth product recall | 2023-08-21
The purpose of the urgent medical device correction notification is to advise healthcare professionals that Berlin Heart is conducting a voluntary correction concerning all Excor cannulae due to the potential of partial or complete breaches of an Excor…
RecallHealth product recall | 2023-08-17
Affected lots exceed the interim acceptable intake limit for N-nitroso-nortriptyline (NNORT) or exceed the acceptable cumulative intake limit for (N-nitrosodimethylamine (NDMA) and NNORT).
RecallHealth product recall | 2023-08-16
Affected lot exceed the acceptable cumulative intake limit for N-nitrosodimethylamine (NDMA) and N-nitroso-nortriptyline (NNORT).
RecallHealth product recall | 2023-08-16
Manufacturer notifying its customers regarding the following four identified system conditions:
Issue 1 - autofill alarms: manufacturer received multiple complaints where Cardiosave IABP users were identifying autofill failure conditions on the devices…
RecallHealth product recall | 2023-08-14
Baxter Corporation is issuing an urgent medical device correction for a subset of novum Iq large volume pumps (LVP) due to reports of pump operators pressing a single key on the novum keypad, but the pump registers the intended key as well as incorrectly…
RecallHealth product recall | 2023-08-14
CHS initiated this recall after receiving a recall notification letter from Baxter which stated the following:
"This action is being taken as a precautionary measure as there may be a potential for the IV solution bags to leak at the connection…
RecallHealth product recall | 2023-08-14
Affected lot exceeds concentration limit for N-nitrosodimethylamine (NDMA).
RecallHealth product recall | 2023-08-14