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new-york-wholesale-group-recalls-zaarah-herbals-rasayan-churan,-zaarah-herbals-gurmar-powder,-zaarah-herbals-vasaka-powder-and-zaarah-herbals-bhringraj-powder-because-of-possible-health-risk FDA
  • March 10, 2025

New York Wholesale Group Recalls Zaarah Herbals Rasayan Churan, Zaarah Herbals Gurmar Powder, Zaarah Herbals Vasaka Powder and Zaarah Herbals Bhringraj Powder Because of Possible Health Risk

New York Wholesale Group of Hicksville, NY is recalling Zaarah Herbals Rasayan Churan, Zaarah Herbals Gurmar Powder, Zaarah Herbals Vasaka…
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…
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
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
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…
power-assist-device-recall:-max-mobility/permobil-removes-speedcontrol-dial-component-used-with-smartdrive-mx2+-power-assist-device-due-to-risk-for-motor-to-be-unresponsive-to-the-user FDA
  • March 3, 2025

Power Assist Device Recall: Max Mobility/Permobil Removes SpeedControl Dial Component Used with SmartDrive MX2+ Power Assist Device Due to Risk for Motor to Be Unresponsive to the User

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial used with SmartDrive MX2+ Wheelchair Power Assist system may be unresponsive to users.