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Medical Devices Discussed by Personal Injury Firm

April 4, 2017 By Altrumedia Leave a Comment

Recalled medical devices discussed by Personal Injury Lawyer, Bennett Long.

Filed Under: Medical Devices, Video

RSS FDA Med Watch

  • Mobile Power Unit AC Power Cord Recall: Abbott Medical Removes AC Power Cord Associated with HeartMate Mobile Power Unit (MPU) Due to Potential Risk of the Cord Not Locking into Place
  • Manual Resuscitator Recall: Ambu Inc. Removes SPUR II Resuscitators Due to Blocked Manometer Port
  • Breathing Circuit Set Recall: Hamilton Medical, Inc. Removes Coaxial Breathing Circuit Set Due to Possible Inner Blue Tube Cracks That May Impact Ventilation
  • Green Lumber Holding, LLC Issues Consumer Alert on Counterfeit Products Following FDA Findings
  • Infusion Pump Correction: ICU Medical, Inc. Issues Correction for Plum Duo Infusion System Due to Software Possibly Resulting in Pump Becoming Unresponsive
  • DermaRite Industries Expands Voluntary Nationwide Recall Due to Potential Burkholderia cepacia Contamination
  • Ventilator Correction: Hamilton Medical AG Corrects HAMILTON-C6 Due to Risk of Ventilation Interruption from Defective Circuit Board

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