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albertsons-companies-stores-in-arkansas,-louisiana,-oklahoma-and-texas-voluntarily-recalls-select-items-containing-tuna-salad-from-reser’s-fine-foods-due-to-an-ingredient-recall-linked-to-possible-listeria-monocytogenes-contamination FDA
  • July 17, 2025

Albertsons Companies Stores in Arkansas, Louisiana, Oklahoma and Texas Voluntarily Recalls Select Items Containing Tuna Salad from Reser’s Fine Foods Due to an Ingredient Recall Linked to Possible Listeria Monocytogenes Contamination

Albertsons, Randalls and Tom Thumb stores in Arkansas, Louisiana, Oklahoma and Texas are voluntarily recalling select items containing tuna salad…
bd-issues-update-to-voluntary-global-recall-of-alaris-and-bd-alaris-pump-modules-serviced-with-legacy-bezel-kit-assemblies FDA
  • July 16, 2025

BD Issues Update to Voluntary Global Recall of Alaris™ and BD Alaris™ Pump Modules Serviced with Legacy Bezel Kit Assemblies

BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today issued a voluntary recall related to…
portable-oxygen-concentrator-car-adapter-recall:-drive-devilbiss-healthcare-removes-igo-dv6x-619-dc-car-adapter-due-to-cord-possibly-becoming-hot-to-the-touch-and/or-melting-while-being-used FDA
  • July 16, 2025

Portable Oxygen Concentrator Car Adapter Recall: Drive DeVilbiss Healthcare Removes iGo DV6X-619 DC Car Adapter Due to Cord Possibly Becoming Hot to the Touch and/or Melting While Being Used

Drive Devilbiss Healthcare is recalling iGo2 DV6X-619 DC car adapter due to complaints of the DC power cord being hot…
early-alert:-microbore-extension-set-issue-from-b-braun-medical-inc. FDA
  • July 16, 2025

Early Alert: Microbore Extension Set Issue from B. Braun Medical Inc.

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
continuous-glucose-monitor-receiver-recall:-dexcom,-inc.-removes-certain-dexcom-g6,-g7,-one,-and-one+-receivers-due-to-speaker-malfunction-that-may-cause-missed-alerts-for-dangerous-blood-sugar-levels FDA
  • July 16, 2025

Continuous Glucose Monitor Receiver Recall: Dexcom, Inc. Removes Certain Dexcom G6, G7, ONE, and ONE+ Receivers Due to Speaker Malfunction That May Cause Missed Alerts for Dangerous Blood Sugar Levels

Dexcom recalls certain receivers that may fail to sound alerts. Missed alerts could delay detection of severe blood sugar events,…
chetak-llc-group-recalls-product-because-of-possible-health-risk FDA
  • July 16, 2025

Chetak LLC Group Recalls Product Because of Possible Health Risk

Are recalling Frozen ‘Deep Sprouted Mat(Moth) 16 oz. and Deep Sprouted Moong 16oz. because they have the potential to be…
cranial-drill-recall:-integra-lifesciences-recalls-codman-disposable-perforators-due-to-risk-of-device-disassembly FDA
  • July 15, 2025

Cranial Drill Recall: Integra LifeSciences Recalls Codman Disposable Perforators Due to Risk of Device Disassembly

Certain Codman Disposable Perforators may disassemble during or after use, increasing the risk of brain injury, hemorrhage, or prolonged surgery.
krasniy-oktyabr-inc.-usa-issues-alert-on-eviscerate-dry-salted-vobla-“aral-silver” FDA
  • July 15, 2025

Krasniy Oktyabr Inc. USA Issues Alert on Eviscerate Dry Salted Vobla “Aral Silver”

KRASNIY OKTYABR INC. USA. of BROOKLYN, NY, is recalling its “ARAL SILVER VOBLA” brand “ARAL”, because the product was found…
early-alert:-infusion-set-performance-issue-from-bd FDA
  • July 14, 2025

Early Alert: Infusion Set Performance Issue from BD

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program.
safety-and-availability-concerns-with-vasoview-hemopro-endoscopic-vessel-harvesting-systems-–-letter-to-health-care-providers FDA
  • July 14, 2025

Safety and Availability Concerns with VasoView HemoPro Endoscopic Vessel Harvesting Systems – Letter to Health Care Providers

The FDA is alerting health care providers to the recall of certain VasoView HemoPro devices due to risk of silicone…