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arterial-catheter-recall:-medline-industries,-lp,-removes-integrated-arterial-catheters-due-to-excess-material-at-catheter-hub-that-may-detach FDA
  • February 6, 2025

Arterial Catheter Recall: Medline Industries, LP, Removes Integrated Arterial Catheters due to Excess Material at Catheter Hub that May Detach

Medline Integrated Arterial Catheters continuously monitor blood pressure. Excess material on the catheter hub that may detach and enter the…
early-alert:-atherectomy-catheter-system-issue-from-bard-peripheral-vascular FDA
  • February 6, 2025

Early Alert: Atherectomy Catheter System Issue from Bard Peripheral Vascular

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
continuous-ventilator-correction:-baxter-healthcare-corporation-issues-correction-for-life2000-ventilator-due-to-a-nonconforming-battery-charger,-which-triggers-a-battery-alarm-and-renders-the-ventilator-inoperable FDA
  • February 5, 2025

Continuous Ventilator Correction: Baxter Healthcare Corporation Issues Correction for Life2000 Ventilator due to a nonconforming battery charger, which triggers a battery alarm and renders the ventilator inoperable

Baxter Healthcare is recalling the Life2000 Ventilator System by correction, due to a defective battery charger making the ventilator inoperable.
fda-alerts-patients-to-regularly-check-diabetes-related-smartphone-device-alert-settings,-especially-following-phone-hardware-or-software-changes FDA
  • February 5, 2025

FDA Alerts Patients to Regularly Check Diabetes-Related Smartphone Device Alert Settings, Especially Following Phone Hardware or Software Changes

The FDA is alerting users of diabetes-related medical devices that smartphones connected to diabetes devices may fail to send critical…
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