Datex-Ohmeda recalls 550 Giraffe Stand-alone Infant Resuscitation Systems (Class I) due to blender knob shaft loosening that may deliver incorrect oxygen concentrations, potentially causing hypoxia or hyperoxia.
Thoratec LLC recalls 694 HeartMate 3 System Controllers (Model 106531US) nationwide and internationally due to 11-volt backup battery failures that may cause temporary or reversible health problems.
Medline Industries recalls 49,654 Class II central line and dialysis dressing change kits nationwide due to defective Mastisol adhesive and butyrate tubing that may crack during use.
Arrow International LLC recalls 1,516 Class I medical kits containing lidocaine, bupivacaine, and sodium chloride due to supplier quality issues and potential sterility compromise that could cause serious injury or death.
Medline Industries recalls 4,801 medical procedure kits nationwide and worldwide due to catheter surface irregularities, premature connector detachment, and diameter specification failures that may cause temporary health problems.
Par Health USA, LLC recalls 46,334 nationwide units of Buprenorphine HCl injection (0.3 mg/mL) due to crystallization classified as a Class II health risk.
Glenmark Pharmaceuticals recalls Alyacen 7/7/7 oral contraceptive tablets nationwide due to out-of-specification impurities that may cause temporary or reversible health problems.
Sandoz recalls 7,803 bottles of Focalin XR 5 mg nationwide due to missing or incorrect lot and expiration date labeling on bottles.
PAI Holdings LLC recalls VistaPharm KERR INSTA-CHAR activated charcoal nationwide due to failure to meet OTC monograph standards, posing risk of temporary or reversible health problems.
Jonco Industries recalls 1,407 jars of White Cheddar Seasoning (1.2 oz) distributed in Mississippi and Wisconsin due to Salmonella-contaminated milk powder; Class I recall.
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