Recalls for 05/27/2015

Bedessee Imports Inc., Voluntarily Recalls Brown Betty Coconut Milk Powder Due to Presence of Undeclared Milk
05/27/2015 Food Recall

Our firm is voluntarily recalling Brown Betty Coconut Milk Powder Mix because the product contains Sodium Caseinate, but the label lacks the allergen statement "Contains 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.

  • Company:
    Bedessee Imports Inc.
  • Problem
    Drowning Hazard
Natural Grocers® issues recall of Macadamia Nuts due to possible health risk
05/27/2015 Food Recall

Vitamin Cottage Natural Food Markets Inc., a Lakewood, Colo., based natural grocery chain, is recalling two lots of Natural Grocers brand Macadamia nuts as the product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

  • Company:
    Vitamin Cottage Natural Food Markets Inc.
  • Problem
    Salmonella
Euro Import Distributions Inc Issues an Alert on Undeclared Sulfites in Dried Apricots
05/27/2015 Food Recall

EURO IMPORT DISTRIBUTIONS INC at 4821 1st Avenue, Brooklyn, NY 11232 is recalling dried apricots in 3.5 oz plastic bags, because it contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

  • Company:
    Fresh Foods Inc
  • Problem
    Entanglement Hazard
Avea Ventilator by CareFusion: Recall - Potential Malfunction of Pressure Transducer
05/27/2015 Medical Recall

Ventilator may activate false Extended High Ppeak or Circuit Occlusion audio and visual alarms, open the safety valve and stop ventilating.

  • Company:
    CareFusion
Carefusion Provides Update on Voluntary Global Recall of Avea® Ventilator
05/27/2015 Food Recall

CareFusion, a BD company (NYSE:BDX), provided an update on a global voluntary recall that was initiated on April 21, 2015 to address an issue with certain units of AVEA® ventilators. The recall has been designated as a Class I recall by the U.S. Food and Drug Administration (FDA), which means the Agency believes that there is a reasonable probability that use of the recalled product will cause serious adverse health consequences or death.

  • Company:
    CareFusion
  • Problem
    Potential malfunction of an AVEA ventilator specific 5 psi pressure transducer