65 results

• Medtronic MiniMed Pump Lawsuit

  January 2, 2026

  Austin Kirk

  Design problems with the Medtronic MiniMed insulin pump have resulted in the recall for certain devices distributed in recent years,...

• Medtronic MiniMed Insulin Pump Recall Over Battery Failure Risks

  October 7, 2024

  Irvin Jackson

  FDA has announced a class I recall impacting tens of thousands of Medtronic MiniMed insulin pumps, due to risks that the battery may deplete rapidly after the device has been dropped or physically impacted.

• Medtronic Video Laryngoscopes Recall Results in “Do Not Use” Warning

  September 9, 2024

  Martha Garcia

  FDA has given a Medtronic video laryngoscope recall a class I designation, following reports that the batteries can overheat and explode, posing a risk of serious injury or death for patients.

• FDA Issues “Do Not Use” Warning for Recalled Medtronic NIM Endotracheal Tubes

  July 10, 2024

  Irvin Jackson

  The FDA is warning healthcare providers not to use Medtronic NIM endotracheal tubes following dozens of reports of the devices losing functionality and degrading, which could prevent life-saving oxygen from being supplied to patients during surgery.

• Medfusion Syringe Pump Recall Issued Over Software Errors

  March 6, 2024

  Hannah Brown

  The FDA has announced a Medtronic Syringe Pump recall affecting more than 85,000 units which may over- or under-deliver insulin and important medications due to software errors.

• Medfusion Syringe Pump Recall Issued After Software Error Linked to Injury Risk

  February 15, 2024

  Hannah Brown

  More than 50,000 Medfusion syringe pumps are being recalled due to potential software errors which could interrupt the delivery of life-saving drugs.

• Cardinal Health Monoject Syringe Recall Issued Over Problems Fitting Drug Pumps

  February 5, 2024

  Katherine McDaniel

  The FDA has announced a recall of certain Cardinal Health Monoject luer-lock and enteral syringes because they may not properly fit drug pumps, potentially leading to medication errors.

• Infusomat, Space Infusion Pump Recall Issued After Alarm Failure Linked to Patient Death

  November 20, 2023

  Hannah Brown

  Nearly 11,000 Braun Medical Infusomat and Space infusion pump battery packs due to occlusion sensor failures which could put patients at risk of serious injury or death.

• Facing Few Alternatives, FDA Has Provided Recommendations for Using Recalled Cardiosave Intra-Aorta Balloon Pumps

  September 1, 2023

  Martha Garcia

  The FDA is giving healthcare providers recommendations on how to continue safe use of recalled Cardiosave Intra-Aorta Balloon Pumps due to a lack of alternative devices on the market.

• Medtronic MiniMed Lawsuit Filed Over Wrongful Death from Insulin Pump Overdose

  August 14, 2023

  Irvin Jackson

  The Medtronic MiniMed lawsuit indicates the insulin pump malfunctioned, delivering a lethal overdose which caused significant pain and suffering before death.