Z-2112-2018 Class II Terminated

Recalled by Baxter Healthcare Corporation — Medina, NY

FDA device recall Z-2112-2018 was initiated by Baxter Healthcare Corporation on May 8, 2018 and is designated Class II. Reason for recall: The firm will be updating the Instructions for Use for the product. Current IFUs instruct users to lower the primary bag 20 inches below the secondary bag using a hanger when performing a secondary… The recall status is terminated (terminated Apr 8, 2019). Affected quantity: 333961.

Recall Details

Product Type
Devices
Report Date
Jun 13, 2018
Initiation Date
May 8, 2018
Termination Date
Apr 8, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
333961

Product Description

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), infusion pump, 35700BAX and 35700ABB Product Usage: The Baxter SIGMA Spectrum Infusion Pump with Master Drug Library is intended to be used for the controlled administration of fluids. These fluids may include pharmaceutical drugs, blood, blood products and mixture of required patient therapy. The intended routes of administration consist of the following clinically accepted routes: intravenous, arterial, subcutaneous, intrathecal, epidural or irrigation of fluid space. Spectrum Infusion Pump is intended to be used in conjunction with legally marketed intravenous administration sets and medications provided by the user. The Spectrum and Spectrum with Master Drug Library is suitable for many user facility applications such as but not limited to hospitals, outpatient care areas, homecare and ambulatory care services. Spectrum and Spectrum with Master Drug Library is intended to reduce operator interaction through automated programming thereby helping to reduce errors associated with complex device programming. Parameter programming requires trained healthcare professional confirmation of limits and drug therapy to the physicians directive.

Reason for Recall

The firm will be updating the Instructions for Use for the product. Current IFUs instruct users to lower the primary bag 20 inches below the secondary bag using a hanger when performing a secondary infusion. However, the firm supplies 12.5-inch hangers with the Baxter disposable secondary sets.

Distribution Pattern

Worldwide Distribution - US Nationwide and the country of Canada.

Code Information

All serial numbers manufactured from 11/1/2005 to 4/22/2013, with release dates 1/1/2005 and forward.

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-2112-2018
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.