5 results

• Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization

  May 27, 2026

  Michael Adams

  Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.

• Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods

  April 30, 2026

  Michael Adams

  Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.

• 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.

• 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.