We’re putting the finishing touches on our new products that will be ready to launch in mid-February. So far, we’ve introduced 2 of those new products on our Facebook page. We will continue to give you sneak peaks at those products in the next couple of weeks but here is what we’ve shown so far:
Blueberry Maple Granola: With tender little blueberries and maple sugar, you’ll love the blend of 2 Canadian tastes!
Berry Delight Trail Mix: This is our new favorite and I have had to hide the samples. It has softy and yummy blueberries, cranberries, raw sunflower seeds and semi-sweet chocolate chips with just a touch of sea salt. Sunflower seeds are a new ingredient for us… but we had so many people asking for them that it was time to give them a try.
Watch our Facebook page as we update posts several times per week. Don’t forget to give us your feedback too.
It’s only been 16 days since the new year but once we opened back up on January 3, we’ve been moving forward on plans to expand the Nonuttin’ team. With 5 new products launching in February and more stores and clients finding Nonuttin’ products all over North America, it’s time to bring some more great staff into the fold.
As of today, we’d like to welcome Gloria who has accepted a position on the production team. They’re the ones who diligently mix, cut and package your favorite Nonuttin’ products. Since we make most of our products in small batches with many of the processes by hand, these people are carefully chosen to ensure the products we make are the best and safest we can deliver.
Coming soon is a new “voice” on the phone in our front office/customer service. Sheila has been doing a great job with help from a couple of us while the lines are ringing but it’s time for her to have some daily support to make sure that our customer service remains top notch. We can’t tell you who that person is just yet but we should be able to annouce the newest member of our team later this week.
We’re excited to be growing to serve you better!
Barry Callebaut USA has recalled Kroger Value brand semi-sweet chocolate chips after chips with dairy in them were mistakenly packed in the non-dairy/Kosher pareve packaging for Kroger. The recall notice may be seen at: http://usfoodsafety.com/02af0007.asp and the kosher alert for dairy can be seen at: http://www.ok.org/alerts.asp
I’m bringing this recall to your attention since you may be aware that Barry Callebaut is the manufacturer who produces our semi-sweet mini chocolate chips and 70% dark chocolate chunks in a peanut/nut free plant and on a dairy free line. Our chocolate is manufactured in the Quebec, Canada, plant however, not in the US and is not affected by this recall.
Further, we test every incoming ingredient for several allergens prior to releasing it into the manufacturing process, with dairy being one of the many tests we perform. If we were to discover dairy in any ingredient, it would be isolated in our warehouse and not be allowed into our production area. We would then work with the manufacturer to discover the source of the contamination problem before ordering any more ingredients from them.
If you have any questions, please let our team know at email@example.com or toll free: 1-866-714-5411.
We’re very lucky that our government in Canada is supportive of small businesses and provides favorable loan programs for the purchase of machinery. Because of a loan through our local Community Futures office, we were able to purchase “Bertha” our packaging machine that puts the packaging around all of our granola bars (we name all of our machinery, including Fabio, our heat shrinker).
Because of that loan a few years ago, we were chosen to be showcased in a series of successful business videos put together by Community Futures BC. That video is now available for viewing on YouTube at: Nonuttin’ Foods on YouTube. Check it out to find out a little bit more about our family business.
FAAMA, The Food Allergy and Anaphylaxis Management Act was passed into law in the United States after being signed by President Obama on Tuesday, January 4, 2011. So what does this Act mean to you as a food allergic parent?
Here is the official summary of the ACT which was introduced in February 2009:
Requires the Secretary of Health and Human Services to develop and make available to local educational agencies, schools, early childhood education programs, and other interested entities voluntary guidelines to develop plans for individuals to manage the risk of food allergy and anaphylaxis in schools and early childhood education programs. Directs that such guidelines address:
(1) parental obligation to provide the documentation of their child’s allergies;
(2) the creation of an individual food allergy management plan for each such child;
(3) communication between schools or programs and emergency medical services;
(4) reduction of exposure to anaphylactic causative agents;
(5) food allergy management training; and
(6) administration of epinephrine.
Allows the Secretary to award matching grants to assist local educational agencies in implementing such food allergy and anaphylaxis management guidelines.
What the law will actually do in its practical application remains to be seen. At the very least, this law should give parents a legal means to fall back on in EVERY state should their school/school district administration not accomodate for their child’s anaphylaxis. Further, it allows for the legal means to give epinephrine, which seems to have been a cause for confusion or inaction in schools.
While there are many teachers and administration who have been wholly supportive of anaphylaxis plans, many parents report to me that they have been treated as second-class citizens in the school system and even have had it suggested that they home school their child. While many allergic parents do pursue this option, it should be by choice, not fear or intimidation. As a former teacher, I can’t imagine that any teacher or school would be apathetic about anaphylaxis but it has been a very real issue for many around the world.
It will take some time for the voluntary guidelines and educational materials to be developed and funding to be provided for training. But in the meantime, a very important first step has been taken for those with anaphylaxis in a school setting.
Just after Christmas I heard that a Chicago teenager had died of anaphylaxis on the last day of school before the Christmas break when she had Chinese food with her classmates. These stories always make me cry because while I cannot understand what it is like to lose a child, I can tell you that I have imagined it more than once. My heart goes out to the family of this child.
From all accounts, this was a child whose parents had well-equipped her for living with her food allergies. School staff had checked on the safety of the food to be served more than once and school officials and classmates were well aware of the peanut allergy. The details have not been released so the public may never know what exactly happened. There is some question of whether epinephrine was injected. The stories indicate that it is against Illinois law for staff to administer epinephrine unless the prescription is specific to the student. If you’d like to know more, you can read the Chicago Tribune article and the Allergic Living article.
I have many questions after reading the accounts; not in the interest of assigning blame but to understand and learn about what I can do with my own child and her school. The accounts indicate that in Illinois students are not allowed to have epipens with them and teachers can’t give another’s epi-pen to a child having a reaction. To me this is highly disturbing. Is this an indication that the fear of liability trumps medically necessary action?
So now you’re wondering, okay Alana, you title says Tragedy and Hope; where’s the Hope part? While we can never bring back these children, we can use these tragedies to better protect all anaphylactic children. After a similar death in an Ontario school, we got Sabrina’s Law. Sabrina’s Law helped provide the background for my province’s anaphylaxis policy and gave allergy advocates around the world a springboard for their own country’s anaphylaxis laws and policies. I have Sara Shannon to thank for making sure that the lessons learned from her daughter Sabrina’s death would not be forgotten. My child has benefited from that advocacy.
To that end, more hope was created yesterday in the US when President Obama signed into law FAAMA. This stands for the Food Allergy and Anaphylaxis Management Act, a national law for all states to protect anaphylactic children in schools. Voluntary guidelines and materials will be created for states to access. You can read the information about what this law means and how it came about on the FAAN website.
I look to these developments with hope to educate all about the very real risks of anaphylaxis and to prevent any more needless deaths.