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A boil water advisory was issued for Moultrie County for the South Shores subdivision, Lakeside Villa subdivision, and surrounding areas going to Wolf Creekon on Feb 13.
Recent Interesting Reports
February 1, 2021 4:52 PM
“Morning recieved: Arm sore. Headache. Then broke out in welt type hives from my face down to my toes. Had to go to ER for epi pen and steroids. ”
February 2, 2021 10:30 PM
“I am a female, 26 years old.An RN at Riley Children’s hospital. I received the moderne vaccine. The first dose, the physical shot was less painful than flu vaccine. Only symptom was sore arm for 2 days. Second dose, much worse. Woke up 24 hrs later feeling fatigued, nauseous, headache, and developed... large red circular rash around injection site. Lasted 24 hours. Was hot to touch and very painful. No fevers. Better the next day. ”
February 5, 2021 8:50 PM
“I received my first vaccine at Alamodome on January 20 and will get second vaccine February 10. The Alamodome was very organized and the people who worked there very professional. I had no reactions to first shot which was Pfizer ”
February 7, 2021 11:58 PM
“The FDA observed the website offers “Corona Destroyer Tea” for sale in the United States in two options, “Prevention” and “Reversal,” and that this product is intended to mitigate, prevent, treat, diagnose, or cure COVID-19 in people.
Based on FDA review, this product is an unapproved new dr... ug sold in violation of section 505(a) of the Federal Food, Drug, and Cosmetic Act (FD&C Act), 21 U.S.C. § 355(a). Furthermore, this product is a misbranded drug under section 502 of the FD&C Act, 21 U.S.C. § 352. The introduction or delivery for introduction of this product into interstate commerce is prohibited under sections 301(a) and (d) of the FD&C Act, 21 U.S.C. § 331(a) and d. Some claims on the website and product label establish the intended use of the product and misleadingly represent it as safe and/or effective for the treatment or prevention of COVID-19
For more information click here: fda.gov ”
I only got a chain from the Blackcass company. I ordered a little battery chainsaw , Spokane, WA, USA
February 10, 2021 6:03 PM
“On 1/20/21 I ordered the little battery chainsaw which is advertised on Facebook all the time. It cost $37.98. I only got a chainsaw blade today. ”
January 28, 2021 6:29 AM
“I ordered the chainsaw on November 5, 2020. I received a chain and a snoring device but no chainsaw. I to thought I was ordering from a company in the United States. It actually states, it was a US company.I saw other ads and purposely used Blackcass thinking it was in this country. I have yet to r... eceive the entire order. I sent a message to the company a few days ago. Awaiting my product. ”
Public Health Alert for Settlers Jerk Beef Jerky Products Due to Undeclared Allergen, California, USA
January 29, 2021 10:45 AM
“The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) beef jerky products due to misbranding and an undeclared allergen. The product may contain anchovies, a known allergen, which is not declared on the product label. F... SIS is issuing this public health alert out of the utmost of caution to ensure that consumers with allergic reactions to anchovies are aware that these products should not be consumed. This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product because of the presence in a product of very small amounts of the undeclared allergens are typically associated with milder human reactions. A recall was not requested because the products are not currently available for sale to consumers.
The RTE beef jerky products were produced from October 20, 2020 through January 12, 2021 and have a one-year shelf life. The product labeled as “CHARLIE BROWN FARMS PREMIUM BEEF JERKY Original Prime Rib” contains Worcestershire, which is not listed as an ingredient, but was utilized in the product formulation. The following products are subject to the public health alert: [View Labels (PDF only)]
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY PEPPERED BEEF”
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY OLD FASHIONED”
4-oz. gold foil bags of “SETTLERS JERKY HOT BEEF”
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY PRIME RIB”
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY RING OF FIRE BEEF JERKY”
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY GHOST PEPPER”
3.25-oz. silver bags of “Sierra Madre Provision Co. OLD FASHIONED BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. PEPPERED BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. HOT BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. GHOST PEPPER BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. RING OF FIRE BEEF JERKY”
3-oz., 4-oz. and 8-oz. silver bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY GHOST PEPPER”
3-oz. and 4-oz. gold bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY Original Prime Rib”
3-oz. and 4-oz. gold bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY RING OF FIRE”
The products bear establishment number “EST. 8275” inside the USDA mark of inspection. These items were distributed for wholesale and also sent to retail locations in California.
FSIS is concerned that some product may be in consumers’ pantries.
The problem was discovered by FSIS inspection personnel. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.
For more info: fsis.usda.gov
Source: FSIS ”
January 29, 2021 10:45 AM
“The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 43 pounds of not-ready-to-eat (NRTE), heat treated, not fully cooked chicken enchilada products due to misbranding and an undeclared allergen. FSIS is issuing this public... health alert out of the utmost of caution to ensure that consumers with allergic reactions to soy are aware that these products should not be consumed. A recall was not requested because the chicken enchilada products are no longer available in commerce.
The NRTE product labeled as “HyVee mealtime CHICKEN ENCHILADAS” was produced on Jan. 3, 2021. The following product is subject to the public health alert: [View Label (PDF only)]
62.4-oz. (3-lbs. 14.4-oz.) heat and serve container of “HyVee mealtime CHICKEN ENCHILADAS” with lot code “21003” and “Best If Use By: 01/10/2021” date on the product label. The products bear establishment number “P51558” inside the USDA mark of inspection. These items were distributed to HyVee retail locations in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.
The problem was discovered when a HyVee retail store employee identified the labeling issue and reported it to the establishment.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
For more info: fsis.usda.gov
Source: FSIS ”
February 10, 2021 10:00 PM
“Company name: NDAL MFG INC
Brand name: ManukaGuard
Product recalled: Allercleanse Nasal Spray
Reason of the recall: Due to Yeast Contamination
FDA Recall date: February 10, 2021
Recall details: NDAL MFG INC is voluntarily recalling one lot of Manukaguard Allercleanse, nasal spray to the consume... r level. The Allercleanse nasal sprays have been found to be contaminated with yeast.
Risk Statement: The use of Allercleanse (manuka honey) nasal spray contaminated with yeasts, in the population most likely to use it (children, adults, and elderly), may result in adverse events that necessitate medical or surgical intervention. However, use of this contaminated product in immunosuppressed individuals may result in life threatening invasive fungal infections.
NDAL MFG INC has not received any reports of adverse events related to this recall. The product is used as a NASAL SPRAY to clean nasal passages and sinuses of irritants and other environmental contaminants and is packaged in cardboard box with one nasal spray per box UPC 858631002128. The affected Allercleanse lot is lot # 2010045 and BB 10/2023 expiration date.
Product was distributed Nationwide in the USA to 1 e-commerce website amazon.com, distributors and retail stores. NDAL MFG INC has notified its distributors and customers by e-mail followed by telephone and further email and has arranged for return/replacement etc. of all recalled products.
Consumers/distributors/retailers that have product which is being recalled should stop using/return to place of purchase/discard/contact their doctor, etc., if they have not already done so. Consumers with questions regarding this recall can contact NDAL MFG INC by phone 1-800-916-1220 or e-mail address SUPPORT@MANUKAGUARD.COM, M-F 7:30 am to 4 pm PST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Check the full recall details on fda.gov
Source: FDA ”
January 29, 2021 12:23 AM
“I reported earlier today that I received the second dose of Pfizer at work Wednesday by CVS, I am now broken out with a wicked rash on both legs, and feet. It’s itchy and looks horrible. Never had a rash like this.
Previous Report: Jan 28, 2021
Took the second... dose of Pfizer at work yesterday given by CVS. CVS worker was good with a needle did not even feel the shot go in-she has that skill mastered. Slight burning for a few moments after potion entered bloodstream. Mildly tender arm- left upper arm where vaccine was given. It was mild enough I did not have to take any PRNs for pain or discomfort. Next morning after vaccine ( this AM) I felt a bit sluggish-no energy-arm still mildly sore-still not having to take a PRN for pain. Not sure if it was from the vaccine or me working 14 hours day before-just put it this way-I work a lot of 14 hour days and was not that sluggish feeling in the AM. Other than that I'm good-no headache, no dizziness, I have been monitoring my temp and I have not had one, my temp runs around 97.3 etc..We are tested for COVID where I work every week due to having a outbreak in our geriatric hospital on all floors killing many of the geriatric patients, staff shortage, nurses, doctors, sick with COVID-so far I am one of only a few staff that has not tested positive for COVID. If I have any symptoms in the next few days from the vaccine I will report. Stay safe!! ”