Tag: food_recalls_fda_drugs

• Ambrosia Brands Recalls Rosabella Moringa Capsules Due to Salmonella Risk

  17 Feb 2026 3:23 p.m. · Source: US Food and Drug Administration

  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

• MR.7 SUPER 700000 Capsules Recalled Due to Undeclared Sildenafil and Tadalafil

  16 Dec 2025 3:28 p.m. · Source: US Food and Drug Administration

  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

• DermaRite Issues Nationwide Recall of DermaKleen, Dermasarra, Kleenfoam, and Perigiene Products

  11 Aug 2025 4:12 p.m. · Source: US Food and Drug Administration

  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

• DermaRite Recalls DermaKleen, DermaSarra, KleenFoam, and PeriGiene Products Due to Contamination

  11 Aug 2025 7:08 a.m. · Source: US Food and Drug Administration

  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

• Dexcom Recalls Glucose Monitor Receivers Due to Malfunctioning Speakers

  17 Jul 2025 3:34 p.m. · Source: US Food and Drug Administration

  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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