FDA recall record

Baxter Corporation Englewood ABACUS TPN Calculation Software, Baxa: 8300-0045 ABACUS CE recall — FDA Z-0539-2014

Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS Total parenteral Nutrition (TPN) Calculation Software versions 2.0 through 3.0…

Class IIclassification
Z-0539-2014official record ID
Dec 25, 2013report date

Recall record at a glance

Official recordZ-0539-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBaxter Corporation Englewood
Report dateDec 25, 2013
Recall initiation dateDec 3, 2013
Quantity2,211
LocationEnglewood, CO, United States

Official product description

ABACUS TPN Calculation Software, Baxa: 8300-0045 ABACUS CE (Calculator Edition), 8300-0046 ABACUS SE (Single-Workstation Edition), 8300-0047 ABACUS ME (Multi-Workstation Edition) ABACUS is a Windows - based order entry TPN software application for comprehensive calculations and label printing. The primary use of Abacus is for TPN order calculations. Other uses of Abacus include: non-TPN volumes administered to patients on TPN therapy in order calculations; CVVH calculations; Cardioplegia (Buckburg) calculations; Epidural calculations; Dilutions from concentrated ingredient; Combinations of multiple ingredients; Fractional doses from larger volumes

Why the product was recalled

Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS Total parenteral Nutrition (TPN) Calculation Software versions 2.0 through 3.0 due to the possibility that a patient could receive another patient's TPN order as a result of data corruption.

Distribution information

Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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Related recall records

Other records from the same recalling company are shown first when available.

Medical DeviceMay 27, 2015

Baxter Corporation Englewood ABACUS SE recall — FDA Z-1628-2015

Baxter Corporation is conducting a field action for the ABACUS SE and ME models due to the possibility that the compounder will load the incorrect formula upon scanning the bag label when…

Class IIFDA: TerminatedBaxter Corporation Englewood