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smiths-medical-issues-urgent-medical-device-correction-informing-customers-of-a-potential-issue-with-certain-sizes-of-intubation-oral/nasal-endotracheal-tubes-being-smaller-than-expected fda
  • March 10, 2025

Smiths Medical Issues Urgent Medical Device Correction Informing Customers of a Potential Issue with Certain Sizes of Intubation ORAL/NASAL Endotracheal Tubes Being Smaller Than Expected

Smiths Medical has issued an Urgent Medical Device Correction to notify affected global customers of a potential issue with the…
adm-recalls-select-pelleted-cattle-nutrition-feed-products fda
  • March 5, 2025

ADM Recalls Select Pelleted Cattle Nutrition Feed Products

ADM Animal Nutrition, a division of ADM (NYSE: ADM), is recalling specific pelleted animal feed products because they may contain…
update-on-alert:-solution-set-issue-from-baxter-healthcare-corporation fda
  • March 5, 2025

Update on Alert: Solution Set Issue from Baxter Healthcare Corporation

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
early-alert:-infusion-pump-issue-from-baxter-healthcare-corporation fda
  • March 5, 2025

Early Alert: Infusion Pump Issue from Baxter Healthcare Corporation

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
update-on-alert:-infusion-pump-software-issue-from-fresenius-kabi-usa fda
  • March 5, 2025

Update on Alert: Infusion Pump Software Issue from Fresenius Kabi USA

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
us.-trading-company-of-hayward,-ca-is-recalling-joy-luck-brand-lily-flowers-because-it-may-contain-undeclared-sulfites fda
  • March 5, 2025

U.S. Trading Company of Hayward, CA is Recalling Joy Luck Brand Lily Flowers Because it May Contain Undeclared Sulfites

U.S. Trading Company of Hayward, CA is recalling Joy Luck Brand Lily Flowers because it may contain undeclared SULFITES. People…
nova-tech,-inc.-issues-voluntary-nationwide-recall-of-lactated-ringers-5-l-injectable-solution-for-veterinary-use-due-to-potential-presence-of-fiber-like-particles fda
  • March 4, 2025

Nova-Tech, Inc. Issues Voluntary Nationwide Recall of Lactated Ringers 5 L Injectable Solution for Veterinary Use Due to Potential Presence of Fiber-like Particles

Grand Island, Nebraska, Nova-Tech, Inc. is voluntarily recalling one (1) lot of Lactated Ringers Injection for Animal Use Only to…
akt-trading-inc.-recalls-prepared-vegetable-products-because-of-possible-health-risk fda
  • March 4, 2025

AKT Trading Inc. Recalls Prepared Vegetable Products Because of Possible Health Risk

AKT Trading Inc. of Torrance, California, is recalling certain prepared vegetable products manufactured by Choshiya Honten Co., Ltd. due to…
endovascular-system-recall:-philips-removes-and-discontinues-distribution-of-tack-endovascular-system-due-to-user-challenges-that-caused-additional-procedures-to-reposition-or-remove-implant fda
  • March 3, 2025

Endovascular System Recall: Philips Removes and Discontinues Distribution of Tack Endovascular System Due to User Challenges That Caused Additional Procedures to Reposition or Remove Implant

Tack Endovascular System is used to repair artery dissection after angioplasty but ongoing user issues led Philips to discontinue use…
vaporizer-recall:-getinge-removes-vaporizer-sevoflurane-quick-fil-and-expands-recall-of-vaporizer-sevoflurane-maquet-filling-due-to-risk-of-patient-and-health-care-professional-exposure-to-toxic-chemical-hydrogen-fluoride fda
  • March 3, 2025

Vaporizer Recall: Getinge Removes Vaporizer Sevoflurane Quick-Fil and Expands Recall of Vaporizer Sevoflurane Maquet Filling due to Risk of Patient and Health Care Professional Exposure to Toxic Chemical Hydrogen Fluoride

Vaporizers Sevoflurane Quick-Fil and Maquet Filling mix oxygen and sevoflurane for anesthesia. This sevoflurane may degrade to toxic hydrogen fluoride.