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oxygen-concentrator-recall:-jiangsu-jumao-x-care-medical-equipment-co-ltd-removes-jmc5a-ni/truaire-5-oxygen-concentrator-due-to-the-devices-spontaneously-catching-fire fda
  • February 5, 2025

Oxygen Concentrator Recall: JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD Removes JMC5A Ni/TruAire-5 Oxygen Concentrator due to the devices spontaneously catching fire

JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD is recalling certain devices due to incidents of device melting and fire during…
pressure-monitoring-device-recall:-medtronic-neurosurgery-issues-correction-for-becker-and-exacta-external-drainage-and-monitoring-systems-due-to-cracks-and/or-leaks-in-stopcocks fda
  • February 3, 2025

Pressure Monitoring Device Recall: Medtronic Neurosurgery Issues Correction for Becker and Exacta External Drainage and Monitoring Systems Due to Cracks And/Or Leaks in Stopcocks

Becker and Exacta EDMS are used for draining and monitoring cerebrospinal fluid in the brain. Stopcocks may have cracks or…
gerber-products-company-announces-recall-and-discontinuation-of-all-batches-of-gerber-soothe-n-chew-teething-sticks-due-to-choking-hazard fda
  • January 31, 2025

Gerber Products Company Announces Recall and Discontinuation of All Batches of Gerber® Soothe N Chew® Teething Sticks Due To Choking Hazard

January 31, 2025 — Gerber Products Company is initiating a recall and discontinuation of all batches of GERBER® SOOTHE N…
blue-ridge-beef-issues-a-recall-of-blue-ridge-beef-natural-mix-due-to-salmonella-contamination fda
  • January 31, 2025

Blue Ridge Beef Issues a Recall of Blue Ridge Beef Natural Mix Due to Salmonella Contamination

January 31, 2025– Blue Ridge Beef is recalling 5,700 lbs. of their 2 lb log Natural Mix due to a…
alvogen-issues-voluntary-nationwide-recall-for-one-lot-of-fentanyl-transdermal-system-25-mcg/h-due-to-a-defective-delivery-system fda
  • January 31, 2025

Alvogen Issues Voluntary Nationwide Recall for One Lot of Fentanyl Transdermal System 25 mcg/h Due to a Defective Delivery System

Alvogen, Inc. is voluntarily recalling one lot of Fentanyl Transdermal System 25 mcg/h transdermal patches to the consumer level. The…
update-on-alert:-infusion-pump-issue-from-fresenius-kabi-usa fda
  • January 31, 2025

Update on Alert: Infusion Pump Issue from Fresenius Kabi USA

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
update-on-alert:-endoscope-accessories-forceps/irrigation-plug-issue-from-olympus fda
  • January 31, 2025

Update on Alert: Endoscope Accessories Forceps/Irrigation Plug Issue from Olympus

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