39 results

• Tandem Mobi Insulin Pump Recall Issued Following Multiple Serious Injuries

  April 23, 2026

  Martha Garcia

  The FDA has decided that a Tandem Mobi insulin pump device correction should be considered a Class I recall following multiple reports of serious patient injuries.

• Medtronic MiniMed Infusion Pump Recall Issued Over Risk of Hypo- or Hyperglycemic Reactions

  April 7, 2026

  Darian Hauf

  Federal health officials have announced a recall impacting more than half a million Medtronic MiniMed insulin pumps after the manufacturer identified a design flaw that may cause the devices to deliver too little or too much insulin.

• Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death

  March 24, 2026

  Michael Adams

  Following reports that some Omnipod 5 insulin pods may malfunction and deliver incorrect insulin doses, attorneys are investigating potential lawsuits involving alleged design defects, inadequate testing, and failure to warn about the risk of these dangerous errors.

• Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA

  March 20, 2026

  Michael Adams

  Omnipod 5 lawsuits are now being investigated following a recall of certain insulin pods over the risk that they may malfunction and deliver incorrect doses.

• Dexcom Wrongful Death Lawsuit Alleges Continuous Glucose Monitor Failed

  November 18, 2025

  Michael Adams

  A Tennessee woman’s lawsuit alleges her husband’s Dexcom CGM failed to detect the fatal hyperglycemia that led to his heart attack.

• Insulin Delivery Problems Lead to Tandem t:slim X2 Insulin Pump Recall: FDA

  August 13, 2025

  Michael Adams

  At least 700 adverse events and nearly 60 injuries have been linked to a potential speaker defect in certain Tandem t:slim X2 insulin pumps.

• Medical Device Manufacturers Often Fail To Submit Timely Adverse Event Reports to FDA: Study

  March 19, 2025

  Martha Garcia

  The findings of a new study indicate that medical device manufacturers turn in a third of all adverse patient event reports later than legally required.

• Medtronic Insulin Pump Air Pressure Issues Could Lead to Dangerously Low Blood Sugar Levels

  March 6, 2025

  Darian Hauf

  A medical device correction was issued by the manufacturer after identifying a design flaw that could lead to the insulin pumps malfunctioning during airplane flights.

• 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.

• Omnipod 5 Android App Recalled Due to Insulin Overdose Risk

  January 9, 2024

  Hannah Brown

  Health officials have announced a recall of nearly 30,000 Omnipod 5 insulin delivery systems due to the potential for the app to register incorrect insulin doses to patients, increasing the risk of serious injuries.