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606 North 9th Street, Canon City, Colorado, United States
Updated: November 24, 2021 12:00 PM
2 individuals tested positive for Covid-19, Washington Elementary School - Fremont County, Fremont County, CO
2 days ago
2 individuals at Washington Elementary School - Fremont County in Fremont county tested positive for Covid-19. The outbreak began on 20-09-2021
14 individuals tested positive for Covid-19, Washington Elementary School - Fremont County, Fremont County, CO
2 weeks ago
14 individuals at Washington Elementary School - Fremont County in Fremont county tested positive for Covid-19. The outbreak began on 20-09-2021
3 individuals tested positive for Covid-19, Washington Elementary School - Fremont County, Fremont County, CO
1 month ago
3 individuals at Washington Elementary School - Fremont County in Fremont county tested positive for Covid-19. The outbreak began on 20-09-2021
1 individual tested positive for Covid-19, Washington Elementary School - Fremont County, Fremont County, CO
1 month ago
1 individual at Washington Elementary School - Fremont County in Fremont county tested positive for Covid-19. The outbreak began on 20-09-2021
Recent Interesting Reports
2 weeks ago
I have been applying since the beginning of the month I went to two different appointments and every three hours the system messes up and thinks that I haven’t done my steps
The Procter & Gamble Company (NYSE: PG) is voluntarily recalling all lots with expiry through September 2023 of specific Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products sold in the United States, and listed in the table below, to the... consumer level due to the presence of benzene detected.
Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Based on exposure modeling and the cancer risk assessments published by the Environmental Protection Agency (EPA) (IRIS database), daily exposure to benzene in the recalled products at the levels detected in our testing would not be expected to cause adverse health consequences. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. To date, The Procter & Gamble Company has not received any reports of adverse events related to this recall and is conducting this recall out of an abundance of caution.
The affected products are used as antiperspirants and hygiene products and are packaged in aerosol cans. See the link below for Product names and UPC codes and images for further descriptions. They are recalling all lots with expiry through September 2023 of the products listed in the link below.
Company name: The Proctor & Gamble Company
Brand name: Old Spice Secret
Product recalled: Old Spice and Secret Aerosol Sprays
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 23, 2021
Check the full recall details on fda.gov
Arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm., USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
1 week ago
I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT
1 week ago
DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.
I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so... far today and STILL pieces of DreamBone Twist Sticks
I am a 42-year-old biologist. I had very good health overall before the injection. I did suffer from seasonal allergies, but otherwise enjoyed a full and active life. I took the first Moderna injection on March 17, 2021. I took the injection because I believed it was... needed to protect myself, my family, and others in my community. I believed the FDA, CDC, and doctors that it was safe, effective, and the right thing to do. I was told that the potential side effects were possible arm pain, headache, and flu like symptoms. The CDC backed up these claims on their website by listing the side effects as minor. I took the first injection on March 17, 2021, at 9:00 a.m. at the pharmacy. A rash appeared on my arm and torso within a couple of hours. Some veins in my arms popped. There was pain on my left arm, like I had been punched. I took Allegra and slept all day from the fatigue. It only got worse from there. My doctors ignored reactions from the injection and unbelievably recommended a second shot! They said it was needed to be safe. I took the second Modern injection on June 17, 2021. After the second injection, I got dizzy right away. I stayed at the pharmacy for thirty minutes because I thought I might faint. I was fearful before the second shot. Enough that I took an EpiPen (although expired) with me as a precaution after the last reaction. Two days after the second injection, I could not even get out of bed. As the day progressed, I couldn’t perform my work on the computer. My eyesight became so blurred that I couldn’t read my email. I was dizzy when I got up. I had no choice but to stay down. That lasted at least two weeks. I still deal daily with fatigue, dizziness, memory problems, nerve pains, joint pains, burning of skin, numb ringing ears, headaches, and tingling sensations in my body. My face droops. My right hand tremors. Everyone involved in the coercion of this injection has badly harmed my daily life, my family, my work, and my health. They have taken ME away. They have taken me away from everything that made my life happy and fulfilling. Before the injection, I lived a normal, active and happy life. I worked full time, took care of my family, rescued dogs, and enjoyed a variety of physical activities. Now, I have an unnamed mysterious disorder which the doctors have told me they suspect is a variation of Guillain Bare. I suddenly have gastro issues and tachycardia. My headaches go back and forth between vestibular migraines and hemiplegic migraines. Those insane migraines take me out for hours, and sometimes days. The extreme inflammation on my brain from cytokine storm affects how I think, walk, and talk. I am unable to do the most basic tasks. Driving is completely out of the question! I cannot even drive myself anywhere, which has rendered me completely dependent on others. The effects of these shots are so extreme and never-ending. So far, no effective treatments have been found to help me. I have seen numerous specialists. I have tried special diets. I have undergone blood tests, PCP visits, neurological visits, ENT visits, cardiologist visits, immunologist visits, and many more. I have found no answers or guidance. There is no trajectory of improvement. No one knows if I will ever get better. This makes me feel really helpless and hopeless sometimes. As soon as I mention that symptoms are “vaccine” related, I feel completely ignored. No doctors want to talk about the possibility of vaccine injury. It took me six months to prove to my family doctor that I have been reacting to the “vaccine”. I spent countless hours, between the migraines and fatigue, researching desperately on my own. I even went over my medical records over the years to understand what is going on with my body. Being ignored by the medical community as well as friends and family that did not have an adverse reaction to the injection has taken a mental toll on me. At least those that live with me know the day-to-day issues and have never doubted the source. Side effects need to be acknowledged more publicly. More research needs to be done before we can push this into our kids or make mandates. Long term data is imperative and the only conscionable thing to do. | Symptoms: Other, Headache, Dizziness, Fatigue, Gas, Joint Pain
#vaccine #moderna #modernacovid19vaccine #covid19vaccine #youngsville #louisiana #unitedstates #headache #dizziness #fatigue #gas #jointpain
NJ post office is a ‘black hole’, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
3 weeks ago
On 9-24-21 I valued package was returned using Pitney Bowes shipping label provided by the merchant (American Mint). It was dropped off at the USPS store in Daytona Beach, picked up by Daytona Beach Post Office on 9-28-21 and retrieved from that Post office by Newgistics (Pitney... Bowes) on 9-30-21. On 10-4-21 it arrived and was dispatched from sorting at the Monroe Township, Middlesex County, New Jersey Post Office. Since then it is missing, in a black hole, unable to be found. This is a shame since this is a product scammed to my mother (senior of 86) who followed every step to have her $149.99 from American Mint and now can not receive her money back since the company has not received the product back. Please address this issue to return what is rightfully my mother's. This is a shame.
Pitney Bowes Returns
Parcel Return Service 56901
Tracking # 4205690192023901007848000000499942
Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... no illnesses reported to date.
During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.
The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.
The full list of affected products is on the link below.
Lot numbers and expiration dates are found on the bottom of each container.
Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.
Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements
Check the full recall details on the FDA website: fda.gov