Tag: product_recall
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George J. Howe Co. Recalls Sunflower Seeds Over Undeclared Cashew Allergens
George J. Howe Co. is recalling 13,619 pounds of sunflower seeds across 24 states due to undeclared cashew allergens, posing a risk to individuals with tree nut allergies. No illnesses reported.
HealthBusinessFederal GovernmentEconomySocial IssuesLegal George J. Howe Co.Sunflower SeedsProduct RecallCashewsTree Nut AllergyFood SafetyPennsylvaniaFood RecallsFDADrugs
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Legacy Snack Solutions Recalls Giant Eagle Pita Chips Over Salmonella Risk
Legacy Snack Solutions is recalling Giant Eagle Baked Pita Chips with Parmesan, Garlic & Herb due to potential Salmonella contamination. The product was sold at Giant Eagle and Market District stores across five states, with no illnesses reported.
HealthBusinessPolitics and GovernmentMedical ScienceFederal GovernmentSocial Issues Product RecallSalmonellaGiant EaglePita ChipsFood SafetyLegacy Snack SolutionsWaukeshaFood RecallsFDADrugs
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Winfield’s Chocolate Bar Recalls Dark Chocolate Products Over Undeclared Milk
Winfield’s Chocolate Bar has recalled five dark chocolate products due to undeclared milk, posing a risk to individuals with milk allergies. The items were sold in Houston, TX, and have since been removed and relabeled.
HealthBusinessPolitics and GovernmentFederal GovernmentLegalSocial Issues Product RecallChocolateMilk AllergyFood Allergen Labeling and Consumer Protection ActHoustonCBSL Commissary LLCFood SafetyFood RecallsFDADrugs
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Boston Scientific Issues Class I Recall and Software Correction for ACCOLADE Pacemakers
Boston Scientific has issued a Class I recall for ACCOLADE pacemakers and CRT-Ps, requiring a critical software update. The FDA warns that failing to correct the devices could lead to early replacement, serious injury, or death.
HealthScience & TechnologyBusinessMedical ScienceComputers and InternetLegalFederal Government Product RecallMedical DevicesBoston ScientificPacemakersFDAHealth and WellnessSoftware UpdateFood RecallsDrugs
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Market of Choice Recalls Vegan Kale Caesar Salad Over Undeclared Sesame Allergen
Market of Choice has issued a recall for its Vegan Kale Caesar Salad in Oregon due to an undeclared sesame allergen. The packaging error poses a serious risk to those with sesame allergies, though no illnesses have been reported.
HealthBusinessPolitics and GovernmentFederal GovernmentMedical ScienceLegalEconomyState Governments Product RecallMarket of ChoiceVegan Kale Caesar SaladSesame AllergenOregonFood AllergiesFood & DrinkFood RecallsFDADrugs
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The a2 Milk Company Recalls Infant Formula Due to Potential Toxin Contamination
The a2 Milk Company has voluntarily recalled three batches of its a2 Platinum Premium infant formula in the US due to potential cereulide toxin contamination. Consumers are urged to stop using the affected batches immediately.
Politics and GovernmentHealthBusinessScience & TechnologyFederal GovernmentEconomyMedical ScienceLegalTrade Product RecallInfant FormulaFood SafetyChildren's HealthThe a2 Milk CompanyBacillus cereusOperation Fly FormulaFood RecallsFDADrugs
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The a2 Milk Company Recalls Select Batches of Infant Formula Due to Toxin Risk
The a2 Milk Company is recalling three batches of its a2 Platinum Premium USA label infant formula due to the potential presence of cereulide, a heat-stable toxin that can cause gastrointestinal illness and dehydration in infants.
HealthBusinessPolitics and GovernmentNew ZealandMedical ScienceFederal GovernmentTradeSocial IssuesAustralasia Product RecallInfant FormulaChildren's HealthFood SafetyThe a2 Milk CompanyCereulideOperation Fly FormulaFood RecallsFDADrugs
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Ambrosia Brands Recalls Rosabella Moringa Capsules Due to Salmonella Risk
Ambrosia Brands is recalling Rosabella Moringa Capsules sold nationwide due to potential Salmonella contamination. The recall includes specific lot numbers with expiration dates from March 2027 to November 2027.
HealthBusiness Product RecallSalmonellaAmbrosia BrandsRosabella Moringa CapsulesDietary SupplementsFood SafetyHealth RiskFood Recalls, FDA, Drugs
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MR.7 SUPER 700000 Capsules Recalled Due to Undeclared Sildenafil and Tadalafil
StuffbyNainax LLC recalls all lots of MR.7 SUPER 700000 capsules after FDA found the product tainted with undeclared sildenafil and tadalafil.
HealthBusinessScience & TechnologyMedical SciencePharmaceuticalsLegal Product RecallStuffbyNainax LLCMR.7 SUPER 700000SildenafilTadalafilErectile DysfunctionHuntsville, TexasFood Recalls, FDA, Drugs
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DermaRite Issues Nationwide Recall of DermaKleen, Dermasarra, Kleenfoam, and Perigiene Products
DermaRite Industries recalls DermaKleen, Dermasarra, Kleenfoam, and Perigiene products nationwide due to Burkholderia cepacia contamination, posing infection risks, especially for immunosuppressed individuals.
HealthBusinessScience & TechnologyMedical ScienceLegal DermaRite IndustriesProduct RecallBurkholderia cepaciaDermaKleenDermasarraKleenfoamPeriGieneFood Recalls, FDA, Drugs
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DermaRite Recalls DermaKleen, DermaSarra, KleenFoam, and PeriGiene Products Due to Contamination
DermaRite Industries recalls DermaKleen, DermaSarra, KleenFoam, and PeriGiene products nationwide due to Burkholderia cepacia contamination, posing a risk of serious infections, especially for immunosuppressed individuals.
HealthScience & TechnologyMedical ScienceSocial IssuesFederal GovernmentPuerto Rico DermaRite IndustriesDermaKleenDermaSarraKleenFoamPeriGieneProduct RecallBurkholderia cepaciaFood Recalls, FDA, Drugs
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Dexcom Recalls Glucose Monitor Receivers Due to Malfunctioning Speakers
Dexcom recalls G6, G7, ONE, and ONE+ glucose monitoring receivers because of speaker issues that may cause missed alerts for dangerous blood sugar levels. The FDA has flagged this as a serious recall.
HealthScience & TechnologyMedical ScienceEurope Dexcomglucose monitoringmedical device recallDexcom G6Dexcom G7Dexcom ONEProduct RecallFood Recalls, FDA, Drugs
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Q’Apel Medical Recalls and Discontinues 072 Aspiration System (Hippo)
Q’Apel Medical Inc. recalls 1,617 units of its 072 Aspiration System (Hippo) due to concerns about the distal tip design. The company has chosen to discontinue the product line.
HealthScience & TechnologyMedical ScienceFederal GovernmentLegalAsia Q’Apel Medical Inc.072 Aspiration SystemHippoProduct RecallFDAMedical DeviceMedWatch