Fresenius Kabi USA is voluntarily recalling Lot 6400048 of Midazolam Injection, USP, 2 mg/2 mL packaged in a 2 mL prefilled single-use glass syringe to the hospital/user level. The product mislabeled as Midazolam Injection,
USP, 2 mg/2 mL contains syringes containing and labeled as Ondansetron Injection, USP, 4 mg/2 mL.

New American Food Products, LLC of Methuen, MA is voluntarily recalling various packaged goods because they contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.

Physio-Control announced today that the company is launching a voluntary field action for specific production lots of Infant/Child Reduced Energy Defibrillation Electrodes (defibrillation electrodes) produced by Cardinal Health.
The company is notifying customers of an issue with the artwork on the defibrillation electrodes, as manufactured by Cardinal Health, which shows incorrect electrode placement for an infant.

Aurora Products, Inc. today announced a voluntary nationwide recall for undeclared MILK allergens. Five (5) Dark Chocolate products produced under the Aurora Natural brand; Private Label brands listed below and various Private Label brands that indicate they are packed by or distributed by Aurora Products, Inc. are affected. Please refer to the Products, Brands and Best If Used By dates list below.

Rucker’s Wholesale and Service Co of Bridgeport, IL is voluntarily recalling all of Uncle Buck’s and Family Choice Dark Chocolate Peanuts packaged in standup twist tie bag, due to the presence of an undeclared milk ingredient. People who have an allergy or sensitivity to milk run the risk of serious or life threatening allergic reaction if they consume this product. No illness associated with this recall has been reported.