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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.
voluntary-recall-of-wild-coast-raw-boneless-free-range-chicken-formula-raw-pet-food-because-of-possible-bird-flu-health-risk fda
  • March 2, 2025

Voluntary Recall of Wild Coast Raw Boneless Free Range Chicken Formula Raw Pet Food Because of Possible Bird Flu Health Risk

Wild Coast LLC dba Wild Coast Raw of Olympia, WA is recalling lots of frozen Boneless Free Range Chicken Formula…
little-leaf-farms-announces-limited-voluntary-withdrawal-of-a-specific-lot-code-of-southwest-salad-kit-due-to-undeclared-fish-and-wheat fda
  • February 28, 2025

Little Leaf Farms Announces Limited Voluntary Withdrawal of a Specific Lot Code of Southwest Salad Kit Due to Undeclared Fish and Wheat

Little Leaf Farms is voluntarily recalling a specific lot code of its Southwest Salad Kits due to the potential presence…
patient-table-correction:-philips-updates-use-instructions-for-allura-and-azurion-systems-due-to-patient-fall-risk-from-incorrectly-positioned-mattresses fda
  • February 28, 2025

Patient Table Correction: Philips Updates Use Instructions for Allura and Azurion Systems due to Patient Fall Risk from Incorrectly Positioned Mattresses

Philips Allura and Azurion interventional fluoroscopy systems are used in operating rooms. Incorrectly positioned mattresses may cause patient falls and…
ablation-catheter-correction:-biosense-webster-updates-use-instructions-for-varipulse-due-to-high-rate-of-stroke-or-transient-ischemic-attack fda
  • February 28, 2025

Ablation Catheter Correction: Biosense Webster Updates Use Instructions for Varipulse due to High Rate of Stroke or Transient Ischemic Attack

Biosense Webster updated Instructions for Use for Varipulse due to higher-than-anticipated incidence of peri-procedural stroke or transient ischemic attack.
endoscope-instrument-recall:-olympus-removes-single-use-guide-sheath-kits-due-to-risk-for-radiopaque-guide-sheath-tip-detaching-during-procedures fda
  • February 28, 2025

Endoscope Instrument Recall: Olympus Removes Single Use Guide Sheath Kits Due to Risk for Radiopaque Guide Sheath Tip Detaching During Procedures

Olympus Guide Sheath Kits collect samples from breathing organs through an endoscope. The tip of the guide sheath may detach…
regard-newborn-kit-recall:-roi-cps,-llc-removes-certain-newborn-kits-due-to-a-recalled-component,-the-neo-tee-t-piece-resuscitator-with-an-undersized-controller-spring fda
  • February 28, 2025

Regard Newborn Kit Recall: ROi CPS, LLC Removes Certain Newborn Kits Due to a Recalled Component, the Neo-Tee T-Piece Resuscitator With An Undersized Controller Spring

ROi newborn kits include Neo-Tee T-Piece Resuscitators. The Neo-Tee may have an undersized controller spring that could affect patient breathing…
natural-dior-llc-issues-voluntary-nationwide-recall-of-vitafer-l-gold-liquid-due-to-presence-of-undeclared-tadalafil fda
  • February 26, 2025

Natural Dior LLC Issues Voluntary Nationwide Recall of Vitafer-L Gold Liquid Due to Presence of Undeclared Tadalafil

February 25, 2025 – Natural Dior LLC, is voluntarily recalling the affected lots of Vitafer-L Gold Liquid, a dietary supplement…
central-admixture-pharmacy-services-(caps)-issues-nationwide-recall-of-phenylephrine-40-mg-added-to-0.9%-sodium-chloride-250-ml-in-250-ml-excel-bags-due-to-visible-black-particulate-matter-in-a-single-sealed-vial fda
  • February 25, 2025

Central Admixture Pharmacy Services (CAPS) Issues Nationwide Recall of Phenylephrine 40 mg Added to 0.9% Sodium Chloride 250 mL in 250 mL Excel Bags Due to Visible Black Particulate Matter in a Single-Sealed Vial

February 24, 2025 – Bethlehem, PA. Central Admixture Pharmacy is recalling three lots of Phenylephrine 40 mg added to 0.9%…
lyons-magnus-recalls-lyons-readycare-and-sysco-imperial-frozen-supplemental-shakes-manufactured-by-third-party-because-of-possible-health-risk fda
  • February 22, 2025

Lyons Magnus Recalls Lyons ReadyCare and Sysco Imperial Frozen Supplemental Shakes Manufactured by Third Party Because of Possible Health Risk

Lyons Magnus LLC (“Lyons Magnus”) today announced that it is voluntarily recalling 4 oz. Lyons ReadyCare and Sysco Imperial Frozen…