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Early Alert: Infusion Pump Software Issue from Fresenius Kabi USA

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program

Neonatal Incubator Correction: GE HealthCare Updates Use Instructions for GE HealthCare Giraffe OmniBed Carestation and Incubator Carestation due to Risk of Patient Formaldehyde Exposure

Newly manufactured Giraffe Omnibed and Incubator Carestations for neonates may put off higher than expected formaldehyde levels for the first…

Mutual Trading Co., Issues Allergy Alert Undeclared Milk in Prepared Monkfish Liver

New York Mutual Trading Co., Inc of Secaucus, NJ is recalling 7.05 oz of Prepared Monkfish Liver (Ankimobo) because the…

Quaker Issues Limited Recall on Undeclared Milk in Pearl Milling Company Original Pancake & Waffle Mix Distributed in 11 States

January 14, 2025 – The Quaker Oats Company today issued a recall of a limited number of two pound boxes…

Outpatient Telemetry Correction: Philips Issues Correction for Monitoring Service Application used with Mobile Cardiac Outpatient Telemetry Due to Potential for Missed Information or Notifications That May Impact Patient Care

Philips Monitoring Service Application processes mobile cardiac telemetry data but failed to send critical data for review by healthcare professionals.

Lifestyle Evolution Voluntarily Recalls NuGo Dark Chocolate Chip and NuGo Dark Pretzel Due to Undeclared Milk

Lifestyle Evolution Inc., is recalling select lots of NuGo Dark Chocolate Chip and Dark Chocolate Pretzel nutrition bars because they…

The Mochi Ice Cream Company LLC Issues Allergy Alert on Undeclared Egg in Peach Mango Sorbet

The Mochi Ice Cream Company LLC, Vernon, California is recalling 1350 cases of Peach Mango Sorbet, because it may contain…

Apna Wholesale Issues Alert on Undeclared Sulfites in “Paras Premium Golden Raisins

Apna Wholesale Inc of Hicksville, NY, is recalling its 7oz and 14oz “Paras Premium Golden Raisins” because they contain undeclared…

FDA Requires Guillain-Barré Syndrome (GBS) Warning in the Prescribing Information for RSV Vaccines Abrysvo and Arexvy: FDA Safety Communication

FDA Requires Guillain-Barré Syndrome (GBS) Warning in the Prescribing Information for RSV Vaccines Abrysvo and Arexvy: FDA Safety Communication