Tag Archives: raw milk products

USA – Raw Milk Again – E.coli O157

E.coli Blog 19243

Two cases of E. coli 0157:H7 in West Michigan have been traced back to consumption of raw milk products from an Ottawa County cow share program. In March, a 31 year old Muskegon County woman became ill after drinking raw milk, and in April, a 6 year old child from Kent County became ill after possible consumption of the raw milk product.

USA – Is Raw Milk Good for You ? – Recall E.coli

E.coli BlogEcoli Istock

Raw milk products from Pure Éire dairy in Othello are being recalled due to the possibility of E. coli contamination.

Dairy owner Richard Smith said the company is voluntarily recalling its organic raw milk products dated June 8 and later. The recalled milk is sold in half-gallon glass and plastic containers and one-gallon plastic containers.

Settler’s Country Market is the only retailer in Grant and Adams counties that sells the recalled milk products

 

Research – FDA Risk Assessment of Listeria monocytogenes in Cheese

FDA FDA

The U.S. Food and Drug Administration announced a draft quantitative assessment of the risk of listeriosis from soft-ripened cheese consumption in the United States and Canada. The risk assessment is a joint effort between FDA and Health Canada. View the Federal Register Notice for the assessment.

The new FDA/Health Canada draft risk assessment found that the risk of listeriosis from soft-ripened cheeses made with raw milk is estimated to be 50 to 160 times higher than that from soft-ripened cheese made with pasteurized milk. This finding is consistent with the fact that consuming raw milk and raw milk products generally poses a higher risk from pathogens than do pasteurized milk and its products.

While raw milk and raw milk products put all consumers at risk, the bacteria they may contain can be especially dangerous to people with weakened immune systems, older adults, pregnant women and children. View guidelines for avoiding illness by choosing milk and milk products carefully.

FDA invites comments that can help FDA and Health Canada improve:

  • the approach used;
  • the assumptions made;
  • the modeling techniques;
  • the data used; and
  • the clarity and transparency of the draft quantitative risk assessment documentation.

To submit comments electronically, go to docket FDA-2012-N-1182 on regulations.gov. The comment period opens February 11, 2013 for 75 days.