Ajanta Pharma USA recalls 6,143 bottles of mislabeled Aripiprazole Tablets USP nationwide due to vials containing Voriconazole instead, a Class II recall posing temporary health risks.
International Food Products Corporation recalls Dairy House Ingredient Systems Vanilla Dairy Powder and two other products (92 bags) distributed to TX, TN, and OK due to potential Salmonella contamination.
Dkiru LLC recalls 13,920 bottles of Adndale Magnesium Glycinate Gummies (UPC 860008784551) due to undeclared melatonin that may cause temporary or reversible health problems.
Greenworld Food Express recalls Al Yaman Halawa Extra Pistachio 907g jars (18 units distributed in MI and NY) due to potential Salmonella contamination posing serious health risks.
Smith & Nephew Class II recall of TRIGEN Proximal Straight Humeral Nail 8/7 X 16 (5 units distributed internationally) due to manufacturing defect causing missing distal holes that may necessitate revision surgery if implanted undetected.
Steris Corporation recalls 4,138 HarmonyAIR A-Series surgical lighting systems worldwide due to potential paint delamination on light heads that may cause temporary health issues.
Abiomed recalls 10,297 Automated Impella Controller units worldwide due to potential software errors that may cause serious injury or death in left ventricular support applications.
BD Connecta Stopcocks (REF 394910) are subject to a Class II recall affecting 2,465,500 units distributed across the U.S. due to Port C connection issues that may cause improper tightening with plastic luer-lok syringes.
Mito Red Light Super Mobile near-infrared therapy device subject to Class II recall nationwide due to lithium-ion battery fire or burst risk.
Steris Corporation recalls 2,101 HarmonyAIR A-Series surgical light units worldwide due to detachable control buttons that may cause temporary health problems.
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