Night time medicine, Circle K, Pensacola, Florida, USA

December 7, 2019 2:48 AM

Pensacola, Florida, United States

Symptoms: Vomiting

night time medicine (like nyquil), I was sick immediately after taking it (within 5 minutes). I threw up 3 times and it was only the medicine capsule

December 20, 2019 12:48 PM

“I was fine all day Wednesday , then I stopped by there at around 11pm. Immediately after I ate the food, I started feeling an itchy throat. The next morning i was coughing up nasty thick brown mucus. I gave myself the day to get better but my symptoms worsened. Today I went to the doctors office and... See Moretested positive for influenza. I know I caught this from one of your employees. See Less”

January 27, 2020 9:34 PM

“I flew from Augusta gerogia on January 25 to Missoula Montana and today I'm very sick anyone else sick The shakes high fever. I just went to hospital it influenza A See Less”

March 5, 2020 1:57 PM

“Sore throat, swollen glands, difficulty swallowing, cough, sneezing See Less”

March 17, 2020 4:03 PM

“I think I had a serious virus in November. Same symptoms.

I was striken with headaches, fever exceptional amounts of coughing and mucous and an unimaginable sore throat for about 5 days in November. I didnt know if I could make my trip to Minneapolis for Thanksgiving, but I went and although had... See Morelack of energy, most symptoms had subsided. See Less”

February 24, 2021 12:00 PM

“Employer is not following CDC guidelines when instructing employees who are working on the 1st floor to attend to patients with Covid-19, while the employees are not provided with personal protective equipment.

Alleged Hazards: 1, Employees Exposed: 3
Source: Osha.gov | Receipt Date: 2020-12-28 See Less”

February 16, 2021 12:00 PM

“1) Employees are exposed to infectious disease in that the employer allows employees who are exhibiting symptoms of COVID-19 such as fever or cough to continue to work and not get tested for COVID-19. 2) Employees are exposed to infectious disease in that the employer does not develop and implement... See Morea routine cleaning schedule to sanitize and disinfect commonly used surfaces and equipment.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-01-26 See Less”

February 16, 2021 12:00 PM

“1) Employees are exposed to chemical hazards in that the employer fails to provide employees with the Personal Protective Equipment needed to clean bathrooms and handle chemicals such as but not limited to gloves. 2) Employees are exposed to infectious disease such as COVID-19 in that the employer d... See Moreoes not require or enforce the use of face coverings by employees or guests. 3) Employees are exposed to health hazards in that the employer allows the growth of mold in guests rooms at the blue mattresses in the rooms by the windows.

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-01-29 See Less”

February 16, 2021 12:00 PM

“1) Employees are exposed to infectious disease such as COVID-19 in that the employer does not require or enforce the use of face coverings by employees per CDC guidelines. 2) Employees are exposed to infectious disease such as COVID-19 in that the employer does not develop or implement methods or pr... See Moreactices to clean and sanitized commonly used surfaces and equipment after an employee has tested positive for COVID-19. 3) Employees are exposed to infectious disease such as COVID-19 in that the employer does not have practices in place to practice social distancing in accordance with CDC guidelines. 4) Employees are exposed to infectious disease such as COVID-19 in that the employer does not provide means and methods for employees to sanitize their hands when handwashing is unavailable.

Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-03 See Less”

February 2, 2021 12:00 PM

“1) Employees are exposed to health hazards related to the employer not cleaning and sanitizing the workplace regularly per CDC (Center for Disease Control and Prevention) guidelines after employees tested positive for COVID-19. 2) Employees are exposed to health hazards in that the employer is allow... See Moreing employees who have tested positive for COVID-19 to work with symptoms of the virus, such as fever. 3) The employer is exposing employees to struck by hazards by allowing employees to operate a forklift (Big Red) on site that does not have a properly functioning brake system.

Alleged Hazards: 3, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-01-07 See Less”

February 2, 2021 12:00 PM

“1) Employees are exposed to infectious disease in that the employer does not enforce the 6 ft. social distancing requirement per CDC guidelines in that the employer does not limit the amount of customers that can enter the store at one time and the employer does not provide shielding (sneeze guards)... See Morein between employees and customers that are required to work in close proximity.

Alleged Hazards: 1, Employees Exposed: 21
Source: Osha.gov | Receipt Date: 2021-01-04 See Less”

February 11, 2021 6:25 PM

“I did very well with my first shot of Moderna. I had no reaction except a very sore arm at the injection sight. See Less”

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 See Less”

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... See Morer 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 See Less”

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. See Less”

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... See MoreSIS 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 See Less”

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[1] in people.

Based on FDA review, this product is an unapproved new dr... See Moreug 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 See Less”

February 11, 2021 11:05 AM

“Dont order any thing from black cass or funny 456 both r scams i order two saws and got two chains thats it i order a fold up scooter from funny456 and got a charger to what i do not know both arw full of crap and iam out money See Less”

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... See Morelarge red circular rash around injection site. Lasted 24 hours. Was hot to touch and very painful. No fevers. Better the next day. See Less”

February 16, 2021 11:55 PM

“The FSA announced the recall of Boots Multivitamins supplements by Boots because they have been incorrectly packed with multivitamins containing iron. This resulted in vitamin K not being present within the supplement and iron incorrectly added to the supplements instead. Iron has not been mentioned... See Moreon the label. This means the product is a possible health risk to individuals who may also be consuming iron supplements in addition to these multivitamins.

FSA advises consumers to stop taking the multivitamin supplements. Instead, return it to the Boots store from where it was bought for a full refund. This recall affects multivitamins sold between 12 and 19 January 2021 only.

- Boots Multivitamins (180 tablets). Item code: 80 57 311. Batch code: 1805 and 1806. Best before: end of November 2022.

This product does not contain vitamin K but does contain iron. Excess supplemental iron can result in gastrointestinal effects such as pain, discomfort, constipation or nausea and vomiting.

Check the full recall details on the FSA website food.gov.uk See Less”

February 11, 2021 5:22 PM

“Got my second Moderna Covid-19 vaccine shot, no side effects this time. A little tired and thirsty but so far so good. See Less”