Recall company profile

Baxter Healthcare Corp. Recalls

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

124recall records
Sep 20, 2017latest record date
Sep 5, 2012earliest record date

Recall history in this database

Classification mix: Class II: 93, Class I: 28, Class III: 3.

Medical DeviceJul 3, 2013

Intermate Infusion Pump recall — FDA Z-1604-2013

Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process…

Class IIFDA: TerminatedBaxter Healthcare Corp.
Medical DeviceJul 3, 2013

Intermate Infusion Pump recall — FDA Z-1603-2013

Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process…

Class IIFDA: TerminatedBaxter Healthcare Corp.
Medical DeviceJul 3, 2013

Coiled Tube Infusors recall — FDA Z-1609-2013

Due to an increase in complaints for leaks at the distal male Luer and Luer cap. Baxter implemented enhancements to the blue winged cap to improve the seal between the cap and the Luer.

Class IIFDA: TerminatedBaxter Healthcare Corp.
Medical DeviceJul 3, 2013

Multirate Infusor Devices recall — FDA Z-1601-2013

Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process…

Class IIFDA: TerminatedBaxter Healthcare Corp.
Medical DeviceJul 3, 2013

Basal/Bolus Infusor recall — FDA Z-1606-2013

Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process…

Class IIFDA: TerminatedBaxter Healthcare Corp.

Understanding this recall history

This page summarizes recall records in which the official source identifies Baxter Healthcare Corp. 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.