FDA Class II Recall of GE HealthCare Patient Monitoring Software
GE Medical Systems Information Technologies recalls 15 units of Portrait Core Services Software V1.0.5 over potential loss of patient monitoring and alarm reset issues.
Recalls & Safety Alerts in Wisconsin
Every recalls & safety alerts report published for Wisconsin, newest first.
FDA Closes Class II Recall of GE HealthCare Patient Monitoring Software
The FDA has terminated recall Z-3037-2026 for PORTRAIT COMPUTE AND CORE SERVICES V1.2, saying the action is complete.
FDA Reports Class II Recall of Merge PACS and Merge OrthoPACS Software on September 2, 2026
On September 2, 2026, the FDA reported a Class II recall of Merge PACS and Merge OrthoPACS software due to a measurement display issue.
Kerry Inc. Recalls Mac & Cheese Over Undeclared Egg Allergen
FDA classifies recall as Class I due to undeclared egg in KC Everyday Mac & Cheese distributed across five states.
FDA Reports Class II Recall of GE Healthcare Electrocardiographs
GE Medical Systems Information Technologies Inc. is conducting an ongoing recall of 163 MAC VU360 units due to a software display issue.
FDA Records Ongoing GE Medical Systems Recall of Four Mobile X-Ray Units
An FDA enforcement report classes the Class II action, over safety-pawl testing after column replacement on Optima amx systems, as ongoing.