Tag: drugs
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FDA Issues Early Alert for Baxter Volara System Circuits Due to Leakage Risk
The FDA has issued an Early Alert regarding Baxter's Volara System single-patient use circuits, which may leak air and medication. This issue can lead to ineffective therapy and patient desaturation.
HealthBusinessScience & TechnologyMedical ScienceLegalSocial Issues BaxterVolara SystemFDAMedical Device CorrectionAir LeakagePatient SafetyMedical DevicesFood RecallsDrugs
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FDA Approves New Kidney Risk Warnings for OTC Weight Loss Drug alli
The FDA has approved new labeling for the OTC weight loss drug alli (orlistat) 60 mg, warning of rare risks including acute kidney injury and kidney stones. Consumers with a history of kidney issues should consult a doctor before use.
HealthPolitics and GovernmentMedical ScienceFederal GovernmentEducation FDAalliorlistatkidney injurykidney stonesweight lossDrug SafetyFood RecallsDrugs
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Clover Hill Dairy Recalls Ricotta Cheese Over Listeria Risk
Clover Hill Dairy has issued a voluntary recall for all Soft Ricotta/Requeson Cheese due to potential Listeria monocytogenes contamination. The cheese, distributed across six states and D.C., may be linked to eight reported infections.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentState GovernmentsLegalSocial Issues Clover Hill DairySoft Ricotta/Requeson CheeseListeria monocytogenesProduct RecallFood SafetyMechanicsville, MarylandFDAFood RecallsDrugs
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Go Raw LLC Expands Pet Food Recall for Low Thiamine in Chicken Recipe
Go Raw LLC has expanded its voluntary recall of Steve’s Real Food Freeze-Dried Chicken Recipe. The recall is due to potentially low thiamine levels, which can cause serious health issues in pets, especially cats.
HealthBusinessPolitics and GovernmentMedical ScienceLegalEducationSocial Issues Product RecallGo Raw LLCSteve's Real FoodFreeze-Dried Chicken RecipeThiamine DeficiencyPet HealthFDAFood RecallsDrugs
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BD Recalls ChloraPrep and FREPP Applicators Due to Fungal Contamination Risk
BD has voluntarily recalled specific lots of ChloraPrep Clear 1 mL and FREPP Clear 1.5 mL applicators due to potential fungal contamination with Aspergillus penicillioides, which could lead to serious infections.
HealthBusinessMedical ScienceLegalEducation Product RecallBDChloraPrepFREPPFungal ContaminationAspergillus penicillioidesMedical DevicesFood RecallsFDADrugs
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Nelson & Isa Lacteos LLC Recalls Requeson Cheese Over Listeria Risk
Nelson & Isa Lacteos LLC is recalling 1lb Requeson Cheese packages sold in New York from May 15-28, 2026, due to potential Listeria monocytogenes contamination. No illnesses have been reported yet.
HealthBusinessPolitics and GovernmentMedical ScienceLegalState GovernmentsFederal GovernmentSocial Issues Nelson & Isa Lacteos LLCRequeson CheeseListeria monocytogenesProduct RecallNew YorkFood SafetyPublic HealthFood RecallsFDADrugs
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BD Recalls ChloraPrep and FREPP Applicators Over Fungal Contamination Risk
BD has recalled specific lots of ChloraPrep and FREPP applicators due to Aspergillus penicillioides contamination. This poses risks of serious infection, sepsis, and death, prompting immediate discontinuation and destruction of affected units.
HealthMedical ScienceFederal GovernmentLegalSocial Issues BDChloraPrepFREPPProduct RecallAspergillus penicillioidesFDAMedical DevicesFood RecallsDrugs
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FDA Issues Early Alert on Hamilton Medical Breathing Circuit Sets
FDA issues an Early Alert regarding Hamilton Medical coaxial breathing circuit sets. Certain lots may not perform as intended, leading to impaired exhalation and four reported serious injuries.
HealthBusinessScience & TechnologyUSAMedical ScienceFederal Government FDAHamilton MedicalBreathing Circuit SetsMedical DevicesEarly AlertRespiratory CompromisePatient SafetyFood RecallsDrugs
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Target Recalls Up & Up Baby Wipes Over Microbial Contamination Risk
Target has recalled its Up & Up baby wipes due to contamination with "Burkholderia cepacia" complex and "Burkholderia gladioli." These bacteria pose a risk of serious infections, especially for vulnerable infants and children. Consumers should return the wipes for a…
HealthBusinessMedical ScienceFederal GovernmentSocial IssuesLegal Product RecallTargetBaby WipesMicrobial ContaminationBurkholderia cepaciaInfant HealthFDAFood RecallsDrugs
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FDA Issues Early Alert for GE HealthCare Infant Resuscitation Systems Over Oxygen Delivery Risk
The FDA has issued an Early Alert for GE HealthCare Infant Resuscitation Systems due to loose blender knob shafts. This defect could cause incorrect oxygen delivery, posing risks of hypoxia or hyperoxia to infants, though no serious injuries are reported.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentLegalSocial Issues GE HealthCareInfant Resuscitation SystemsFDAMedical DevicesOxygen ConcentrationProduct RecallPatient SafetyFood RecallsDrugs
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Target Recalls Up & Up Baby Wipes Over Bacterial Contamination Risk
Target is recalling Up & Up baby wipes due to contamination with Burkholderia cepacia complex and Burkholderia gladioli. These bacteria can cause serious infections, especially in vulnerable populations. Consumers should stop use and return products for a full refund.
HealthBusinessMedical ScienceLegalEconomySocial Issues TargetUp & Up Baby WipesProduct RecallBurkholderia cepacia complexBurkholderia gladioliFDAConsumer ProductsFood RecallsDrugs
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Haleon Recalls Gas-X Extra Strength Softgels Over Potential Coolant Contamination
Haleon is recalling four lots of Gas-X Extra Strength Softgels due to potential coolant contamination. Consumers should check lot numbers and contact Haleon for returns, though no adverse events have been reported.
HealthBusinessMedical ScienceLegalEconomySocial Issues HaleonGas-X Extra Strength SoftgelsProduct RecallPropylene GlycolFDADrugsWarren, N.J.Food Recalls
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Prime Food Processing Recalls "Dried Herring Fish" Over Botulism Risk
Prime Food Processing LLC is recalling "Dried Herring Fish" due to inadequate evisceration, violating regulations and posing a botulism risk. The product was distributed in multiple states, though no illnesses have been reported.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentState GovernmentsTradeAgriculture Prime Food Processing LLCDried Herring FishProduct RecallBotulismFood SafetyNew York Department of Agriculture and MarketsVietnamFood RecallsFDADrugs
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FDA, CDC Investigate Listeria Outbreak Linked to Recalled Requeson Cheese
An ongoing FDA and CDC investigation links a multi-state Listeria outbreak, causing 8 illnesses and 1 death, to recalled Clover Hill Dairy requeson cheese. Consumers are urged to avoid the product and clean contaminated surfaces.
HealthPolitics and GovernmentBusinessFederal GovernmentMedical ScienceSocial IssuesAgricultureEducation Listeria monocytogenesRequesonSoft Ricotta CheeseClover Hill DairyFDACDCProduct RecallFood SafetyOutbreak InvestigationFood RecallsDrugs
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Haleon Recalls Gas-X Extra Strength Softgels Due to Chemical Contamination
Haleon has recalled specific lots of Gas-X Extra Strength Softgels due to potential contamination with a diluted propylene glycol-based coolant. Consumers are advised to stop use and contact Haleon for reimbursement, though no adverse events have been reported.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentLegal Gas-XHaleonProduct RecallChemical ContaminationSoftgelsFDAPharmaceuticalsFood RecallsDrugs
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FDA Issues Early Alert on Insulet Omnipod Insulin Pump Under-Delivery Risk
The FDA has issued an Early Alert concerning Insulet Omnipod insulin pumps. Certain Pods may have a cannula tear, leading to insulin under-delivery. Affected models include Omnipod 5, DASH, and Eros, prompting a customer removal recommendation.
HealthBusinessScience & TechnologyMedical ScienceFederal Government InsuletOmnipodInsulin PumpFDAMedical DeviceProduct RecallInsulin Under-deliveryFood RecallsDrugs
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Becton Dickinson Issues Correction for Spinal Trays with Bupivacaine Ampules
Becton Dickinson is correcting BD Spinal Trays by removing bupivacaine ampules due to quality issues and potential ineffectiveness. The FDA deems this a serious recall, warning of risks like infection or reduced anesthetic effect.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentEconomy Becton DickinsonBD Spinal TraysBupivacaineHuons Co. Ltd.FDAProduct RecallAnesthesiaFood RecallsDrugs
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Total Nutrition Expands Recall of Moringa Capsules Over Salmonella Risk
Total Nutrition has expanded its recall of TNVitamins and Doctor's Pride Ultra Potent Complete Green Superfood Moringa Capsules due to potential Salmonella contamination, posing serious health risks. Customers should dispose of products and seek refunds.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentSocial IssuesEducation SalmonellaProduct RecallTotal NutritionTNVitaminsDoctor's PrideMoringa CapsulesFDAFood RecallsDrugs
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Total Nutrition Inc. Expands Recall of Moringa Capsules Over Salmonella Risk
Total Nutrition Inc. has expanded its recall of TNVitamins and Doctor's Pride Ultra Potent Complete Green Superfood Moringa Capsules due to potential Salmonella contamination. The products were sold nationally online, posing serious health risks, especially to vulnerable populations.
HealthBusinessMedical ScienceEconomySocial IssuesLegal Total Nutrition Inc.Product RecallMoringa CapsulesSalmonellaFood SafetyDietary SupplementsDeer Park, NYFood RecallsFDADrugs
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FDA Recommends Alternatives to Hintermann Ankle Replacement System Due to Failure Risks
The FDA advises considering alternative treatments to the Hintermann Series H3 Total Ankle Replacement System due to elevated long-term risks. Device failure, revision surgery, and polyethylene fracture are among the concerns for the DT MedTech LLC product.
HealthPolitics and GovernmentMedical ScienceFederal GovernmentLegalSocial Issues Hintermann Series H3Total Ankle ReplacementFDADT MedTech LLCDevice FailureRevision SurgeryPolyethylene FractureFood RecallsDrugs
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FDA Warns of Blood Clot Risk with Abiomed Introducer Kits
The FDA has issued an Early Alert for Abiomed's 14Fr Low Profile Introducer Kits due to a high rate of complaints regarding thrombus formation. This issue has led to three serious injuries, prompting Abiomed to recommend removal of all affected…
HealthBusinessScience & TechnologyMedical ScienceFederal GovernmentLegal AbiomedFDA14Fr Low Profile Introducer KitThrombus FormationMedical DeviceProduct RecallPatient SafetyFood RecallsDrugs
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Champion Foods Recalls Motor City Pizza Co. 5 Cheese Bread Over Salmonella Risk
Champion Foods recalls Motor City Pizza Co. 5 Cheese Bread due to potential Salmonella contamination. The voluntary recall stems from a milk powder recall, though no illnesses are reported, taken out of caution for consumer safety.
HealthBusinessPolitics and GovernmentFederal GovernmentMedical ScienceAgricultureSocial Issues Product RecallFood SafetySalmonellaChampion FoodsMotor City Pizza Co.Cheese BreadMichiganFood RecallsFDADrugs
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KayserBetten Issues Urgent Correction for IDA Pediatric Care Beds Amid Serious Injury Risk
KayserBetten is correcting its IDA pediatric care beds due to a serious entrapment risk, identified as a Class I recall. A free hand control replacement with automatic locking will be provided to prevent injury or death.
HealthBusinessMedical ScienceLegalSocial Issues KayserBettenIDA pediatric care bedsProduct RecallClass I RecallMedical DeviceChild SafetyEntrapment RiskFood RecallsFDADrugs
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Better Weather Fix Elixir Recalled Due to Undeclared Potent Substances
Better Weather Actives LLC has issued a nationwide recall for all lots of its Better Weather Fix Elixir. The product contains undeclared Mitragynine and its potent derivative, Mitragynine Pseudoindoxyl, posing risks of severe adverse effects, including respiratory suppression and addiction.
HealthBusinessMedical ScienceLegalSocial Issues Product RecallBetter Weather Fix ElixirMitragynineMitragynine PseudoindoxylKratomSheridan, WyomingUS Food and Drug AdministrationFood RecallsFDADrugs
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Dexcom Recalls Stolen G7 Glucose Sensors Following Third-Party Theft
Dexcom has recalled two lots of G7 continuous glucose monitoring sensors, 1725204004 and 1725069002, after they were stolen during destruction and sold by unauthorized third parties, posing risks of infection or device failure. Users should seek replacements.
HealthBusinessLaw EnforcementMedical ScienceLegalEducationEconomySocial Issues DexcomG7 sensorsProduct RecallMedical DevicesDiabetesTheftPharmsource LLCFood RecallsFDADrugs
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Better Weather Actives Recalls Elixir Over Undeclared Mitragynine and Potent Derivative
Better Weather Actives is recalling all lots of its Fix Elixir nationwide due to undeclared Mitragynine and its potent derivative, Mitragynine Pseudoindoxyl, posing risks of severe health effects and addiction. Consumers should stop use and return the product.
HealthBusinessMedical ScienceLegalEducationSocial Issues Product RecallBetter Weather Fix ElixirMitragynineMitragynine PseudoindoxylDietary SupplementsFDAConsumer SafetyFood RecallsDrugs
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FDA Updates Erbe Flexible Cryoprobe Recall with More Lot Numbers
The FDA updated its recall of Erbe Flexible Cryoprobes, adding more affected lot numbers. This Class I recall warns of serious injury or death if devices are used without correction, urging customers to contact Erbe USA with questions.
HealthBusinessMedical ScienceFederal Government Product RecallFDAErbe USAFlexible CryoprobesMedical DevicesPublic SafetyHealth WarningFood RecallsDrugs
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Philips Updates Nebulizer Guidance for Trilogy Evo Ventilators Amid Recall Clarification
Philips has updated guidance for nebulizer use with Trilogy Evo Ventilators, clarifying recall reasons. The FDA's Class I recall now permits non-pneumatic nebulizers under specific placement, with no new serious injuries reported since May 27.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentLegal PhilipsTrilogy Evo VentilatorsNebulizerFDAProduct RecallMedical DevicesVentilator CorrectionFood RecallsDrugs
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SkinnyDipped Almond Bites Recalled Over Undeclared Peanut Allergen Risk
Bazzini, LLC recalls SkinnyDipped Dark Chocolate Coconut Almond Bites nationwide due to undeclared peanuts, posing a serious risk to those with peanut allergies. Consumers should check lot codes and return affected products for a refund.
BusinessHealthSocial IssuesLegalFederal Government Bazzini, LLCSkinnyDippedProduct RecallPeanut AllergyFood SafetyAlmond BitesFood & BeveragesFood RecallsFDADrugs
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DE DIOS’S ICE POPS II LLC Recalls Popsicles Over Undeclared Allergens
DE DIOS’S ICE POPS II LLC is recalling D’DIOSES FRUIT POPS in NJ, NY, PA, CT due to undeclared milk, nuts, and artificial colors. This recall affects products made before April 27, 2026, posing allergy risks.
HealthBusinessMedical ScienceLegal Product RecallDE DIOS’S ICE POPS II LLCD’DIOSES FRUIT POPSAllergensPopsiclesFood SafetyNew JerseyFood RecallsFDADrugs