Baxter Corporation Englewood Recalls

Overview of recall records associated with Baxter Corporation Englewood, including dates, categories and classifications where available.

2recall records

Oct 12, 2016latest record date

Feb 10, 2016earliest record date

Recall history in this database

Classification mix: Class II: 1, Class I: 1.

Medical DeviceOct 12, 2016

Baxter Corporation Englewood 0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter recall — FDA Z-0007-2017

Baxter Healthcare Corporation is issuing a voluntary product recall for all unexpired lots of the 50mm 0.2 Micron Filter (Product Code: H93835) due to the potential for the filter membrane…

Class IFDA: TerminatedBaxter Corporation Englewood

Medical DeviceFeb 10, 2016

Baxter Corporation Englewood Baxter, RAPIDFILL Syringe Strip, 10 ml recall — FDA Z-0731-2016

All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging claim for 12-month shelf life on released product.

Class IIFDA: TerminatedBaxter Corporation Englewood

Understanding this recall history

This page summarizes recall records in which the official source identifies Baxter Corporation Englewood as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.