Tag: product_recall
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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
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Mogo Moringa LLC Recalls Capsules Over Potential Salmonella Risk
Saint Louis-based Mogo Moringa LLC has voluntarily recalled specific lots of its Moringa Capsules due to a possible Salmonella contamination concern. This precautionary measure was taken in coordination with the FDA, advising consumers not to use affected products.
HealthBusinessPolitics and GovernmentLegalSocial IssuesFederal Government Mogo Moringa LLCMoringa CapsulesProduct RecallSalmonellaFDASaint Louis, MissouriFood SafetyFood RecallsDrugs
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Insulet Issues Medical Device Correction for Omnipod Pods Over Insulin Under-Delivery Risk
Insulet Corporation announced a voluntary medical device correction for specific Omnipod Pods due to a manufacturing issue that could cause insulin under-delivery, potentially leading to high blood glucose or DKA. Approximately 7 million Pods are affected.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentEconomyLegal Insulet CorporationOmnipodMedical Device CorrectionInsulin Under-deliveryDiabetic KetoacidosisProduct RecallActonFood RecallsFDADrugs
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Total Nutrition Inc. Recalls Superfood Capsules Over Salmonella Risk
Total Nutrition Inc. has recalled TNVitamins and Doctor’s Pride Superfood Moringa Capsules nationally due to potential Salmonella contamination. Consumers are urged to dispose of affected products and seek refunds.
HealthBusinessMedical ScienceEconomyLegalSocial Issues Product RecallSalmonellaTotal Nutrition Inc.Dietary SupplementsMoringaFDACDCFood RecallsDrugs
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SKS Copack Recalls Specialty Beverages Over Salmonella Contamination Risk
SKS Copack has recalled various specialty beverages across 25 states due to potential Salmonella contamination. The organism can cause serious infections, especially in vulnerable populations. Consumers should check lot codes for affected products.
HealthBusinessLaw EnforcementMedical ScienceSocial IssuesTransportation SKS CopackProduct RecallSalmonellaSpecialty BeveragesFood SafetyCerritosCaliforniaFood RecallsFDADrugs
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JXK Enterprises Recalls "Boner Bears Chocolate" Over Undeclared Sildenafil
JXK Enterprises, Inc. recalls "Boner Bears Chocolate" nationwide due to undeclared sildenafil, an active ingredient in Viagra. This poses serious health risks, especially for individuals with heart conditions or those taking nitrate medications.
HealthBusinessMedical ScienceFederal GovernmentLegalEconomy JXK Enterprises Inc.Boner Bears ChocolateProduct RecallSildenafilFDASexual EnhancementHealth RiskFood RecallsDrugs
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Raaw Energy Recalls Dog Food Due to Listeria Contamination, Halts Production
Raaw Energy has issued a voluntary recall for various dog food products manufactured between July 2025 and March 2026 due to potential Listeria contamination. The company has temporarily halted production to implement enhanced safety measures.
HealthBusinessPolitics and GovernmentUSAMedical ScienceFederal GovernmentState GovernmentsLegalAgriculture Raaw EnergyDog FoodProduct RecallListeria monocytogenesFood SafetyNortheast USPet HealthFood RecallsFDADrugs
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FDA Issues Class I Recall for Medline Namic Manifolds Over Serious Health Risks
The FDA has issued a Class I recall for Medline Namic Manifolds and related kits due to particulate in the fluid path. This poses a serious risk of injury or death if introduced into blood circulation, prompting immediate removal of…
HealthBusinessMedical ScienceFederal GovernmentLegal Product RecallMedlineNamic ManifoldsFDAClass I RecallMedical DevicesPatient SafetyFood RecallsDrugs
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JXK Enterprises Recalls Boner Bears Chocolate Over Undeclared Sildenafil
JXK Enterprises is recalling Boner Bears Chocolate, Lot #BB21125, due to undeclared sildenafil, an active ingredient in Viagra. This poses serious health risks, especially for those on nitrate medications, potentially causing dangerous blood pressure drops.
HealthBusinessUSAMedical ScienceLegalEducationSocial Issues JXK EnterprisesBoner Bears ChocolateSildenafilProduct RecallFDAErectile DysfunctionHealth RiskFood RecallsDrugs
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FDA Alerts Public to Heart Pump Controller Issue from Abiomed
The FDA has issued an early alert regarding Abiomed's Automated Impella Controller, which may restart due to a software error, causing a temporary halt in heart pump support for patients. Abiomed has released updated use instructions.
HealthBusinessScience & TechnologyPolitics and GovernmentMedical ScienceFederal GovernmentLegalComputers and Internet AbiomedAutomated Impella ControllerAICImpellaFDAMedical Device RecallProduct RecallFood RecallsDrugs
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Hometown Food Company Recalls Birch Benders Pancake Mix Due to Undeclared Egg
Hometown Food Company has issued a voluntary recall for a specific lot of Birch Benders Sweet Potato Pancake & Waffle Mix nationwide. The recall is due to undeclared egg, posing a risk to individuals with egg allergies.
BusinessHealthEconomyMedical ScienceLegalSocial Issues Product RecallFood & BeveragesAllergensEgg AllergyBirch BendersHometown Food CompanySweet Potato Pancake MixFood RecallsFDADrugs
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Kettle Cuisine Recalls Minestrone Soup Over Undeclared Shrimp Allergy Risk
Kettle Cuisine recalls Whole Foods Market Kitchen Minestrone Soup due to undeclared shrimp, a serious allergen risk. Distributed across 18 states and online, the 24oz cups with Lot Code 1762181 are affected. No illnesses reported.
HealthBusinessMedical ScienceEconomyFederal GovernmentSocial Issues Product RecallFood SafetyAllergy AlertShrimpMinestrone SoupKettle CuisineWhole Foods MarketFood RecallsFDADrugs
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FDA Announces Serious Recall of React Health VOCSN V+Pro Ventilators
The FDA announced a serious recall of React Health VOCSN V+Pro Ventilators due to a manufacturing defect causing potential oxygen leaks. This could lead to reduced oxygen delivery, increased fire risk, and serious patient harm or death.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentLegalSocial Issues React HealthVOCSN V+Pro VentilatorsVentilator RecallFDAOxygen LeakMedical DevicesProduct RecallFood RecallsDrugs
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Recall Issued for WAP Sensual Enhancement Capsules Over Undeclared Drug Ingredients
Best Supplements Best Prices recalls WAP Sensual Enhancement capsules nationwide due to undeclared sildenafil, tadalafil, and flibanserin, posing serious health risks, especially for those on nitrate medications or consuming alcohol.
HealthBusinessScience & TechnologyMedical ScienceLegalEconomySocial Issues Product RecallWAP Sensual EnhancementBest Supplements Best PricesSildenafilTadalafilFlibanserinDietary SupplementsFood RecallsFDADrugs
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Recall Issued for WAP Sensual Enhancement Capsules Over Undeclared Drug Ingredients
Best Supplements Best Prices recalled WAP Sensual Enhancement capsules nationwide due to undeclared sildenafil, tadalafil, and flibanserin. These ingredients pose serious health risks, including dangerous blood pressure drops and severe drowsiness, especially for individuals on certain medications or consuming alcohol.
HealthBusinessPolitics and GovernmentFederal GovernmentMedical ScienceLegal Product RecallWAP Sensual EnhancementBest Supplements Best PricesSildenafilTadalafilFlibanserinFDAFood RecallsDrugs
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Kroger Homestyle Cheese Garlic Croutons Recalled Due to Salmonella Concern
Sugar Foods LLC is recalling Kroger Homestyle Cheese Garlic Croutons due to potential Salmonella contamination from a milk powder ingredient. The recall, initiated May 15, 2026, affects 5oz pouches, though no illnesses have been reported.
HealthBusinessMedical ScienceLegalAgricultureEconomy Product RecallSalmonellaFood SafetyKroger Homestyle Cheese Garlic CroutonsSugar Foods LLCCalifornia Dairies Inc.Milk PowderFood RecallsFDADrugs
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Nassar Investment Co. Recalls Malazi Tahina Over Salmonella Risk
Nassar Investment Co., LLC. has recalled Malazi Tahina 1Kg bottles due to Salmonella contamination. The affected product, distributed in MI and NC, carries a serious health risk, especially for vulnerable individuals. Consumers should discard it immediately.
HealthBusinessLaw EnforcementMedical ScienceLegalAgriculture Product RecallFood SafetySalmonellaTahinaNassar Investment Co.North CarolinaMichiganFood RecallsFDADrugs
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Recall Issued for WAP Sensual Enhancement Capsules Over Undeclared Drug Ingredients
Best Supplements Best Prices is recalling WAP Sensual Enhancement capsules nationwide. The product contains undeclared sildenafil, tadalafil, and flibanserin, posing serious health risks, especially for those with heart conditions or when combined with alcohol. Consumers should stop use immediately.
HealthBusinessMedical ScienceFederal GovernmentSocial Issues Best Supplements Best PricesWAP Sensual EnhancementProduct RecallSildenafilTadalafilFlibanserinDietary SupplementsFood RecallsFDADrugs
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Straus Family Creamery Recalls Organic Ice Cream Over Metal Fragment Risk
Straus Family Creamery is recalling select organic ice cream due to potential metal fragments. Consumers in 17 states should discard affected pint and quart sizes with specific 'best by' dates. No injuries reported; contact the company for replacements.
BusinessHealthFederal GovernmentLegalAgricultureSocial Issues Straus Family CreameryIce CreamProduct RecallMetal FragmentsFood SafetyOrganic ProductsFood RecallsFDADrugs
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Blackstone Products Recalls Parmesan Ranch Seasoning Over Salmonella Risk
Blackstone Products has issued a voluntary recall for specific lots of its Parmesan Ranch seasoning due to potential Salmonella contamination, linked to a dry milk powder recall. No illnesses have been reported, but consumers should dispose of affected products.
HealthBusinessMedical ScienceSocial IssuesLegal Product RecallFood & BeveragesSalmonellaBlackstone ProductsParmesan Ranch seasoningWalmartProvidence, UtahFood RecallsFDADrugs
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Terra Medi LLC Recalls Smoked Herring Amid Botulism Concerns
Terra Medi LLC has issued a recall for its Karagounis Bros – Hellas Meze Golden Smoked Whole Herring due to improper evisceration, which could lead to botulism. The product was distributed in MA, NJ, IL, and NY, with no illnesses…
HealthBusinessLaw EnforcementMedical ScienceLegalEducation Product RecallTerra Medi LLCSmoked HerringBotulismFood SafetyNew YorkFood ContaminationFood RecallsFDADrugs
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HH Fresh Trading Recalls Enoki Mushrooms Over Listeria Contamination Risk
HH Fresh Trading is recalling 120 cases of 150g Enoki Mushrooms distributed in Texas and Florida due to potential Listeria monocytogenes contamination, prompting a public health warning and urging consumers to return affected products.
HealthBusinessMedical ScienceLegalAgriculture HH Fresh TradingEnoki MushroomsProduct RecallListeria monocytogenesFood SafetyTexasFloridaFood RecallsFDADrugs
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IQ Produce Recalls Enoki Mushrooms Over Listeria Contamination Risk
IQ Produce is recalling 528 cases of 150g Enoki Mushrooms due to potential Listeria monocytogenes contamination, identified by an FDA sample. Consumers should return the product for a refund, though no illnesses have been reported yet.
HealthBusinessMedical ScienceFederal GovernmentAgricultureLegal IQ ProduceEnoki MushroomsListeria monocytogenesProduct RecallFood SafetyVernon, CAFDAFood RecallsDrugs