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Displaying 1 - 13 of 13 items.

" " Novum Iq Large Volume Pump Unapproved Adhesive
Baxter Corporation is issuing an urgent medical device correction for specific Novum Iq LVPs where an unapproved adhesive was used in error during service for the re-installation of the slide clamp assemblies, which can result in in the slide clamp not…
RecallHealth product recall | 2023-11-08
" " Novum Iq Large Volume Pump Operator's Manual
Baxter Corporation has updated the Novum Iq Large Volume Pump (LVP) operator's manual to include the risks associated with use of specific radio-frequency identification devices (RFID) in conjunction with the Novum Iq LVP. Recall start date: October…
RecallHealth product recall | 2023-11-08
" " Novum Iq Large Volume Pump Keypads
On 08Aug2023, Baxter issued an urgent medical device correction for a subset of Novum Iq LVPs due to reports of malfunctioning keypads that were identified within a single manufacturing lot. Customers with pumps from this specific lot were contacted.…
RecallHealth product recall | 2023-11-07
" " Novum Iq Lvp
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
" " Novum IQ Large Volume Pump
Baxter is issuing an urgent medical device correction for the Novum IQ Large Volume Pump (LVP) due to the potential for internal screws becoming loose and damaging the pumping mechanism valves.  Recall start date: July 26, 2023
RecallHealth product recall | 2023-08-02
" " Minicap Disconnect Cap With Povidone-Iodine
Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals.  Baxter is expanding the urgent medical…
RecallHealth product recall | 2023-05-10
" " Novum IQ Large Volume Pump
Through ongoing internal testing, Baxter Corporation has observed isolated incident of over infusion on the Novum IQ LVP infusion pump during test runs at 0.1 ml/hr after 40 hours of continuous infusion within the 96-hour set change interval. Baxter…
RecallHealth product recall | 2023-02-06
" " Novum Iq Large Volume Pump (LVP)
Baxter Corporation is issuing an urgent medical device correction related to two different software issues that occur during use. The first issue observed is due to incorrect reported delivered volume while an infusion is running. The second issue…
RecallHealth product recall | 2022-12-09
" " EM2400 Exactamix Valve Set
Baxter is issuing an urgent medical device correction communication regarding the potential for leaking valves in the Exactamix 2400 valve sets. Baxter has observed an increase in complaints for leaking of ports 1 and 2 when in the closed position,…
RecallHealth product recall | 2022-07-25
" " Minicap Extended Life Pd Transfer Set Clamps
Baxter Corporation is issuing an urgent medical device correction for the Minicap Extended Life Pd Transfer Sets. The following products may cause damage if they come into direct contact with the transfer set: Cleaning products such as hand sanitizer and…
RecallHealth product recall | 2022-01-24
" " Novum Iq Lvp
Baxter Corporation has internally identified a scenario on the Novum IQ Large Volume Infusion Pump (lVP) where 1) an unintended second bolus or 2) an unintended second auto-programming order update may be delivered to the patient. Baxter Corporation has…
RecallHealth product recall | 2022-01-04
" " Sigma Spectrum Infusion Pump With Master Drug Library (V8 Platform)
Baxter is communicating important safety information for Spectrum V8 and Spectrum IQ Infusion Pumps related to potential reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of…
RecallHealth product recall | 2022-01-04
" " Spectrum Iq Infusion System With Dose Iq Safety Software
Baxter is communicating important safety information for Spectrum V8 and Spectrum IQ Infusion Pumps related to potential reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of…
RecallHealth product recall | 2022-01-04
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