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    NEWS

    DRUGS & DEVELOPMENTS

    MARKET INTEL by PharmaCompass

    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.
    All News #Library

    Enforcement Report - Week of February 4, 2026

    FDA

    FDA Issues Form 483 to Baxter Oncology

    FDA

    Enforcement Report - Week of September 3, 2025

    FDA

    Health Canada Issues Recalls of Baxter`s NaCl injection

    HEALTH CANADA

    Enforcement Report - Week of November 13, 2024

    FDA

    Enforcement Report - Week of September 11, 2024

    FDA

    Baxter Issues Voluntary Nationwide Recall for Heparin Sodium 0.9% NaCl Injection

    FDA

    Baxter Issues Urgent Medical Device Recall for Life2000 Ventilator

    FDA

    Enforcement Report - Week of February 28, 2024

    FDA

    FDA Issues Form 483 to Baxter Pharmaceuticals India

    FDA

    Enforcement Report - Week of December 13, 2023

    FDA

    Enforcement Report - Week of October 25, 2023

    FDA

    Health Canada Issues Recall of Baxter`s Sodium Chloride Injections: Solution bags may be leaking in affected lots.

    HEALTH CANADA

    Health Canada Issues Recall of Baxter`s 5% Dextrose Injection, USP: Solution bags may be leaking in affected lots

    HEALTH CANADA

    Health Canada Issues Recall of Baxter`s Gentamicin(E) Sulfate: Solution bags may be leaking in affected lots

    HEALTH CANADA

    Health Canada Issues Recall of Baxter`s Metronidazole Injection, USP: Solution bags may be leaking in affected lots

    HEALTH CANADA

    Baxter Pharmaceuticals India Pvt. Ltd. on Health Canada Inspection List

    HEALTH CANADA

    Enforcement Report - Week of September 6, 2023

    FDA

    Baxter Healthcare Corporation Receives FDA Warning Letter

    FDA

    Health Canada Issues Recall of Baxter`s Sodium Chloride Injections

    HEALTH CANADA

    Health Canda Issues Recall of Baxter Corporation`s 0.9% Sodium chloride inj; Bags leaking

    HEALTH CANADA

    Enforcement Report - Week of August 24, 2022

    FDA

    Health Canada Issues recall of Baxter Corporation Heparin Sodium and 0.9% Sodium Chloride Injection: leak in intravenous bag

    HEALTH CANADA

    Health Canada Issues Recall of Baxter Corporation Heparin Sodium and 0.9% Sodium Chloride Injection

    HEALTH CANADA

    Enforcement Report - Week of November 18, 2020

    FDA

    Baxter Expands Voluntary Nationwide Recall to Include Second Lot of Nexterone Injection Due to Presence of Particulate Matter

    FDA

    Health Canada Issues Recall of Baxter Corporation`s Dianeal PD4 CAPD

    FDA

    Enforcement Report - Week of July 31, 2019

    FDA

    Health Canada Issues Recall of Baxter Corporation Extraneal solution

    HEALTH CANADA

    Enforcement Report - Week of January 16, 2019

    FDA

    Enforcement Report - Week of November 14, 2018

    FDA

    Enforcement Report - Week of October 3, 2018

    FDA

    Enforcement Report - Week of September 26, 2018

    FDA

    Enforcement Report - Week of September 5, 2018

    FDA

    Health Canada Issues Drug Recall of Baxter Corp`s Magnesium Chloride Powder for Solution

    FDA

    Enforcement Report - Week of February 7, 2018

    FDA

    Baxter Expands Voluntary Nationwide Recall to Include Second Lot of Nexterone Injection

    FDA

    US FDA Issues Form 483 to Baxter Healthcare Corporation (Drug Manufacturer)

    FDA

    Baxter Corporation Recalls Dianeal PD4 CAPD Solution With 1.5% Dextrose And 2.5meq/L Calcium

    HEALTH CANADA

    Baxter Issues A Voluntary Nationwide Recall For One Lot of Nexterone Injection

    FDA

    Enforcement Report - Week of November 1, 2017

    FDA

    Baxter Initiates Voluntary Nationwide Recall of One Shipment of Intralipid 20% IV Fat Emulsion

    FDA

    Enforcement Report - Week of July 19, 2017

    FDA

    Enforcement Report - Week of May 24, 2017

    FDA

    Baxter Corporation Is Issuing A Voluntary Product Recall For 1 lot of REVACLEAR Due To The Presence Of Particulate Matter Within The Blood Side Of The Dialyzer

    HEALTH CANADA

    US FDA Enforcement Report- 1/June/2016

    FDA

    US FDA Enforcement Report- 18/May/2016

    FDA

    Baxter Healthcare Corp. recalls 0.9% Sodium Chloride Irrigation due to presence of insect

    FDA

    Baxter Issues Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Solution for Irrigation Due to Presence of Particulate Matter

    FDA

    Baxter initiates Voluntary Nationwide Recall of Select Lots of IV Solutions Due to the Potential for Leaking Containers and Particulate Matter

    FDA

    Baxter IV Solutions: Recall - Potential Presence of Particulate Matter

    FDA

    Baxter Healthcare recalls 0.9% Sodium Chloride Injection due to Presence of Particulate Matter

    FDA

    Recall: Baxter`s Clinimix (2015-06-19)

    HEALTHY CANADIANS

    Baxter Healthcare Corp initiates Class II recall of Heparin Sodium and Sodium chloride injection due to Subpotent Drug

    FDA

    Baxter Initiates Class I Recall of Sodium Chloride Injection

    FDA

    Baxter Initiates Voluntary Recall Due to the Presence of Particulate Matter

    FDA

    Baxter recalls more than half a million units of saline

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