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FDA MEDWATCH ALERTS

December 18, 2014

0.9 Percent Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container by Baxter: Recall - Particulate Matter

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FDA MedWatch Recall - Particulate Matter

November 21, 2014

FDA MedWatch - Respironics California, Esprit V1000 and V200 Ventilators: Class I Recall - Power Failure May Occur

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FDA MedWatch Respironics California Esprit V1000 and V200 Ventilators Class I Recall

November 21, 2014

FDA MedWatch - Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter: Recall - Mislabeled

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Highly Concentrated Potassium Chloride Injection 10 mEq per 100 mL by Baxter Recall Mislabeled

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Maquet SERVO-i Ventilator Battery Module: Class 1 Recall - Battery Run Time Shorter Than Expected

Wednesday, May 08, 2013

AUDIENCE: Anesthesiology, Biomedical Engineering, Nursing, Risk Managers

ISSUE: Some battery modules distributed after Jan. 31, 2010 have a shorter battery run time than expected. This can result in unexpected ventilator shut downs, which can result in serious adverse health consequences, including death. This recall covers 90,000 battery modules distributed in the United States between 02/15/2010 and 11/19/2012.

BACKGROUND: Battery modules allow device users a possibility to operate the SERVO-i ventilator during intra-hospital transportation. The SERVO-i system is used to treat and monitor patients ranging from neonates to adults with respiratory failure or insufficiency.

RECOMMENDATION: Customers are instructed to change the power source to AC and replace the battery modules if either “low battery voltage” or “replace battery” messages are displayed. Customers are instructed to complete and return a Field Safety Notice Confirmation Form by email to FieldAction@maquet.com or via fax at (973) 807-1832.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

  • Complete and submit the report Online: www.fda.gov/MedWatch/report.htm1
  • Download form2 or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

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