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Baxter Corporation Englewood

Complete recall history across all FDA and CPSC categories — 9 total recalls

Baxter Corporation Englewood appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (9)

FDA medical device enforcement actions by Baxter Corporation Englewood

Date Product Reason Class
Aug 24, 2016 0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter is a bacter... Baxter Healthcare Corporation is issuing a voluntary product recall for all u... Class I
Dec 21, 2015 Baxter, RAPIDFILL Syringe Strip, 10 ml. For use with RAPIDFILL Automated Syr... All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging c... Class II
Apr 8, 2015 ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation Editi... Baxter Corporation is conducting a field action for the ABACUS SE and ME mode... Class II
Dec 29, 2014 Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Cap... Self-Righting Luer Tip Caps were manufactured and shipped with a missing late... Class II
Dec 4, 2014 Self-Righting Luer Lock Tip Cap, Green and Self-Righting Luer Slip Tip Cap, Y... Baxter Corporation initiated a recall of two lots of Self-Righting Luer Lock ... Class II
May 28, 2014 Abacus 3.1, Pharmacy Calculator Product Usage: Provide pharmacy calculati... Baxter Corporation is initiating a field correction following an upgrade to A... Class II
Apr 16, 2014 RAPIDFILL Syringe Strip, For use with RAPIDFILL Automated Syringe Filler (ASF... Possible breach in sterile barrier for inner and outer bags of the product. Class II
Apr 2, 2014 ABACUS TPN Calculation Software, Product Codes: 8300-0045 ABACUS CE (Calculat... 1. ABACUS v3.1 may calculate quantities of electrolytes that are double the e... Class I
Dec 3, 2013 ABACUS TPN Calculation Software, Baxa: 8300-0045 ABACUS CE (Calculator Editio... Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS To... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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