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gas-powered-emergency-resuscitator-recall:-mercury-medical-removes-neo-tee-t-piece-resuscitator-due-to-an-undersized-spring-in-the-controller-that-may-prevent-the-device-from-delivering-the-required-pressure-levels-needed-for-effective-ventilation FDA
  • January 31, 2025

Gas Powered Emergency Resuscitator Recall: Mercury Medical Removes Neo-Tee T-Piece Resuscitator Due to An Undersized Spring in The Controller That May Prevent the Device from Delivering the Required Pressure Levels Needed for Effective Ventilation

Mercury Medical recalls the Neo-Tee T-Piece Resuscitator due to the controller potentially not delivering the pressure levels needed for effective…
update-on-alert:-nephroscope-sheath-issue-from-trokamed-gmbh FDA
  • January 31, 2025

Update on Alert: Nephroscope Sheath Issue from Trokamed GmbH

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
update-on-alert:-fluid-delivery-set-issue-from-medline FDA
  • January 31, 2025

Update on Alert: Fluid Delivery Set Issue from Medline

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
update-on-alert:-extracorporeal-blood-circuit-issue-from-nuwellis FDA
  • January 31, 2025

Update on Alert: Extracorporeal Blood Circuit Issue from Nuwellis

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
united-natural-trading-llc-announces-allergy-alert-for-undeclared-milk-in-fresh-direct-dark-chocolate-covered-pretzels FDA
  • January 31, 2025

United Natural Trading LLC Announces Allergy Alert for Undeclared Milk in Fresh Direct Dark Chocolate Covered Pretzels

January 29, 2025 – United Natural Trading LLC, Edison, NJ, is voluntarily recalling Fresh Direct Dark Chocolate Covered Pretzels due…
glucose-and-glucose/ketone-meter-correction:-nova-biomedical-corporation-issues-software-correction-for-statstrip-glucose-and-glucose/ketone-hospital-meters-due-to-risk-for-transmission-of-incorrect-patient-results FDA
  • January 30, 2025

Glucose and Glucose/Ketone Meter Correction: Nova Biomedical Corporation Issues Software Correction for StatStrip Glucose and Glucose/Ketone Hospital Meters Due to Risk for Transmission of Incorrect Patient Results

StatStrip Hospital Glucose and Ketone Meters provide blood glucose and ketone readings in health care settings. A software issue may…
cybersecurity-vulnerabilities-with-certain-patient-monitors-from-contec-and-epsimed:-fda-safety-communication FDA
  • January 30, 2025

Cybersecurity Vulnerabilities with Certain Patient Monitors from Contec and Epsimed: FDA Safety Communication

The FDA is raising awareness about cybersecurity vulnerabilities with Contec CMS8000 and Epsimed MN-120 patient monitors.
olympus-issues-medical-device-advisory-notice-to-use-alternative-devices-to-the-maj-891-forceps/irrigation-plug FDA
  • January 30, 2025

Olympus Issues Medical Device Advisory Notice to Use Alternative Devices to the MAJ-891 Forceps/Irrigation Plug

Olympus Corporation has announced a voluntary Advisory Notice for the Forceps/Irrigation Plug (Isolated Type) model MAJ-891 related to the risk…
wismettac-asian-foods-issues-allergy-alert-on-undeclared-milk-in-curvee-puffs-corn-puff-snack FDA
  • January 29, 2025

Wismettac Asian Foods Issues Allergy Alert on Undeclared Milk in Curvee Puffs Corn Puff Snack

Wismettac Asian Foods, Inc., Santa Fe Springs, CA is expanding its January 17, 2025 recall of 2.46 oz packages of…
new-york-wholesale-group-recalls-zaarah-herbals-shatavari-powder-because-of-possible-health-risk FDA
  • January 27, 2025

New York Wholesale Group Recalls Zaarah Herbals Shatavari Powder Because of Possible Health Risk

New York Wholesale Group of Hicksville, NY is recalling Zaarah Herbals Shatavari Powder, to the consumer/user level because it has…