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Boil Water Advisory, Danville, KY, USA

July 9, 2021 2:34 PM

Danville, Kentucky, United States

A boil water advisory has been issued for addresses from 5096 Perryville Road to Old School House Road, including Parkville Cross Pike, Needmore Road and Salt River Road in the city of Danville. During a boil water advisory, it is recommended that customers boil for three minutes any tap water they intend to use for consumption, such as for drinking, cooking or making ice.

Source: wtvq.com

Reported By SafelyHQ.com User

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“This establishment has had several positive cases of COVID-19 within two weeks time (Managers) and another tested positive today. Needs to be cleaned thoroughly before allowing others to continue to work or shop.

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LONG TERM continued extreme immune response to Pfizer vaccine, Danville, PA, USA

Symptoms: Fever Other Chills Chest Pain Swelling Dehydration
Danville, PA, USA

May 12, 2021 5:59 PM

“I am going to post my entire diary. Those who truly want to know won't mind reading the entire thing and...it's still not over yet.

Pfizer 51 day systemic reaction
(now beyond day 77)
Danville, PA


*Not a complaint*
(wasn't at the time)

I had left prior... See More short term reviews on both doses, now I am finally able to detail my entire reaction which was shocking to me honestly. Arthritis/fibro/immune compromised patients be advised.

After dose 1 on 3 Mar, it simply made my left hand ballooned then arthritic (never had arthritic hands before this) and it seemed as if it was going to relent, but kept coming and going, then eventually this spread to both hands and ankles. I gained 3 pounds of water weight. The pain was maddening from day 8 on, coming and going.

Day 12 I had routine nonsteroidal spinal injections. MISTAKE. I wouldn't advise doing this but it was urgent as I needed the injections to have the capability to drive to dose 2. My whole left side's injection sites swelled and scabbed over several days. (never had that happen in 12 years of receiving them) I could not sit down, lie down, or touch the sites but it resolved quickly in my opinion. The hand pain stayed the course until...

Dose 2 I was thankful to receive and looked forward to my newfound freedom. 1 Apr I had the minor eye floaters on the way home just like dose 1. I felt like a dead dog so fell asleep on the couch as soon as I walked through the door. 7 hours later developed chills and mild fever and leg (quads) pain. No big deal I thought as this happens to everyone. I began consuming electrolytes and rode the fever out with the aid of Ibuprofen. My last review ended with me saying I expect a 1 to 2 day recovery. That is not what really happened.

Following dose 2 ( lot # EP7534) I suffered an entire body inflammatory response.
The leg pain became so severe I had difficulty walking or doing anything at all for 8 days. Any attempt at physical activity doubled the pain. This is when I had my first Dr appointment and I was told to be patient and it should resolve in 2 to 4 WEEKS, and if not I need to be tested for Rheumatoid. I waited patiently and prayed for this to end. As a former athlete, I will admit to being way less sore after running a marathon.

The legs began to ease up but it traveled back to my hands, then to my lower back, then to my knees and feet. Called our Covid hotline at least 4 times during the 3 week course of this barrage and was told that this kind of reaction is almost unheard of. It then hit my hips. This was so excruciating for a week I had to lift my legs by hand to get up, and once again I could walk but didn't desire to. Next doctor appointment, was advised if the pain will not resolve in a timely manner, I need a full examination and bloodwork for gout and 7 other tests were ordered.

While laid up, incidentally my Father received dose 1 of Moderna. He was symptom free until Day 8, then, had the exact same reaction but on a lesser scale. It was then I started to believe something in our genetics is causing it. Day 52, it FINALLY began subsiding. The swelling reduced and became localized to the right knee (prior injury) and the left hand.

Overall, this was a severe reaction but I do not solely blame the vaccine. I am a 43 year old woman with Fibromyalgia and a slew of other compromising health issues. These companies did their ultimate best to save lives, perhaps mine included. Although devastated to seemingly have permanent damage to the knuckles of my left hand, tissue of the right knee and knuckles of my foot, there has been far greater devastation from Covid, including losing a family member.

I am extremely hesitant towards the booster, but I need the protection to feel at peace with sending my children back to school. I will follow my doctor's advice and the Covid team's direction to fill out the VAERS surveys for both doses. This information is found in small print on the back of the card.

*CONTINUED*

It did NOT end here either. 48 hours after the joint pain "subsided," I went to bed thinking it was all over then woke up in Tachycardia shortly after midnight with a heart rate of 156! ? For 3 days I had my daughter sleep in my bed with me as I battled a severely irregular heart beat. This was preposterous as I spent decades as a personal trainer and thought (knew!) I had a very healthy heart?

On the 3rd day of being stuck in chronic tachycardia episodes, my daughters ended up urgently calling family and an ambulance because I felt symptoms of a possible stroke.

In the ambulance my BP had escalated to 167/110 and normal for me is actually always quite low. In fact I had a reading of 117/74 the week prior during an unrelated visit. I have never had a high blood pressure reading in my entire life not from any illness or activity ever!

At the hospital I was informed my kidneys had astonishingly dropped to less than 40% of function and I was in real trouble. They stabilized me and sent me home, then a day later I went right back into tachycardia for an additional 3 days. I did the equivalent of a marathon or more each night IN MY SLEEP. I was given a heart monitor to record the activity and set up with an urgent echocardiogram and CT of my heart. With a blood clotting disorder, I could not afford to mess around any longer and had to leave my kids once again to be driven to the ER. 7 additional hours I spent with a pulse often above 150. I was finally given a Beta blocker and also an antibiotic, as the dehydration this was causing me erupted into a kidney infection which was throbbing on my right side.

I feared for me life. I feared for my vitality as my Pain treatments were stripped away due to the suspected heart condition. All my heart tests came back completely normal and I was told my heart is oddly not the source of my heart condition. A relief yes, but just further proof of how extremely and completely this vaccine attacked my body.

I was having chest pains the week prior and the week of these attacks which was finally concluded to be new Costochondritis, a rare flareup which can happen with Fibromyalgia. Thank God that's all it is but I am so through with this vaccine now and the utter devastation it has caused my entire body. I am having trouble breathing and the umpteen hospital visits have ruled out everything else. It is not anxiety but I will admit alas I have begun to grow impatient with this!! I have 1/2 dozen medical professionals in contact with me daily now working on a way to get me to the finish line.

After clearing my heart tests, I was reinstated for Pain Management and was brought in immediately for an appointment. My back underwent approximately 30 trigger point injections and there was not a location on my body without a muscle spasm. My last injections were rejected by my body due to the presence of the vaccine and I prayed this time they wouldn't be. During the procedure I suffered an immediate inflammatory response, elevated blood pressure, etc etc. My skin reacted so badly my administrator could not even apply the bandages. 13 years getting these injections and no problems until right now!

Next day it started happening all over again. My body (more specifically, the vaccine within my body) began to reject some of my treatment in the lower region. I am now being put on a steroid to combat the vaccine and widespread pain reaction of the chest, legs, hips, extremities, and back. I continue to take the Beta blocker now as well.

10 weeks of suffering I just want it to end but more importantly I have to stay vigilant in getting my story told. I'm willing to bet a reaction like this will turn out not to be so rare. In fact my Father is still laid up just the same as me he's in week 5 battling Moderna and also on a long road. My final report to the CDC will be submitted after further bloodwork, but it is to be made absolutely clear that if I have now developed an auto-immune condition...the vaccine triggered it.

Good luck to everyone but honestly weigh the decision heavily before you enter the unknown.
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Covid-19 OSHA Complaint, Albatross, 312 Railroad Avenue, Suite A, DANVILLE, CA, 94526, USA

Albatross, 312 Railroad Avenue, Suite A, DANVILLE, CA, 94526, USA

May 6, 2021 12:00 PM

“1. The employer did not ensure to exclude COVID-19 cases from the workplace until the return to work criteria subsection (c)(11) has been met. T8 CCR 3205(c)(10)(A). 2. The employer did not ensure to exclude employees from the workplace who have been exposed to a positive COVID-19... See More case. T8 CCR 3205(c)(10)(B).

Alleged Hazards: 2, Employees Exposed: 1
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Boil Water Advisory, 200 Seaton Dr, Russell, KY 41169, USA

200 Seaton Dr, Russell, KY 41169, USA

August 5, 2021 9:10 AM

“*Water Alert*
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Recent Interesting Reports

July 11, 2021 10:50 AM

“Yeah I never received this item I would like my money back, Ordered off of Facebook got from yeahyard a miniature saw pruner
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August 3, 2021 12:02 AM

“Company name: Je Dois L’avoir Boutique
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Reason of the recall: Product contains sibutramine
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Recall details: Hanford, California, Je Dois L’avoir Boutique is voluntarily recalling all of the 365 Skinny... See More High Intensity Pills and or 365 Skinny Emergency Boutique, 30 day capsules supply to the retail/consumer level. The 365 Skinny High Intensity Pills and 365 Skinny Emergency Boutique have been found to contain Sibutramine which is a controlled substance by the DEA and poses significant health risks to consumers both products are from the same manufacturer 365 Skinny is the strongest form and the 365 Skinny Emergency is for people with high blood pressure, diabetes but not limited to other chronic illnesses.

Risk Statement: The 365 Skinny High Intensity Pills and 365 Skinny Emergency Boutique potentially can cause serious health risks such as seizures, tachycardia, palpitations, heart attacks and allergic reactions. Risks associated with this product are more likely with people who have high blood pressure, thyroid disease, men or woman over 65 or children under 16 years old. Je Dois L’avoir Boutique has not received any reports of adverse events related to this recall.

The product is used together with diet and exercise to assist with weight loss and is packaged in bottles of 30 capsules 600mg per capsule. All lots and expiration dates of any of these products are being recalled. Je Dois L’avoir is recalling ALL 365 Skinny High Intensity Pills and 365 Emergency Boutique that it has sold to the public as seen below. Je Dois L’avoir is notifying its distributors and customers by email and is arranging for return/replacement etc. of all recalled products. Consumers that have 365 High Intensity Skinny or 365 Skinny Emergency Boutique which is being recalled should stop using/return to place of purchase/discard/contact Je Dois L’avoir Boutique Immediately.

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July 19, 2021 3:02 PM

“Company name: Pfizer
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Long-term ingestion of N-nitroso-varenicline may be associated with a theoretical potential increased cancer risk in humans, but there is no immediate risk to patients taking this medication. The health benefits of stopping smoking outweigh the theoretical potential cancer risk from the nitrosamine impurity in varenicline. Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time.

Chantix is a treatment to help patients quit smoking and is intended for short term use. People who smoke cigarettes are 15 to 30 times more likely to get lung cancer than people who do not smoke. Smoking is also associated with many other cancers. CHANTIX has a safety profile that has been established over 15 years of marketing authorization and through a robust clinical program. Pfizer believes the benefit/risk profile of CHANTIX remains positive. Patients currently taking Chantix should consult with their doctor to confirm if they received an affected lot, and if appropriate, about alternative treatment options.

To date, Pfizer has not received any reports of adverse events that have been related to this recall.

The product lots were distributed nationwide to wholesalers and Distributors in the United States and Puerto Rico from June 2019 to June 2021. 

For more recall details including the NDC, Lot Number, Expiration Date, and Configuration details for Chantix Tablets check: fda.gov

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July 13, 2021 8:00 PM

“Company name: Innoveix Pharmaceuticals, Inc.
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FDA Recall date: July 13, 2021
Recall details: Innoveix Pharmaceuticals, Inc. is voluntarily recalling the following lots... See More of sterile compounded drug products, within expiry. The products are being recalled due to a lack of assurance of sterility. These concerns arose following a routine inspection of the pharmacy by FDA.

Administration of a drug product intended to be sterile, that is not sterile, could result in serious infections which may be life-threatening. To date, Innoveix Pharmaceuticals, Inc. has not received any reports of adverse events related to this recall. This voluntary recall is being conducted out of an abundance of caution and to promote patient safety, which is the pharmacy's highest priority.

The affected products are injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg. The products can be used for various indications as prescribed. The products can be identified by an Innoveix Pharmaceuticals, Inc. label. The products were distributed in glass vials contained in a small 3 inch by 3 inch white box.

Products were distributed nationwide to both customers and/or medical facilities. A full list of the affected products with the applicable lot numbers and expiration dates is as follows:

Product Lot/Expiry
Semorelin / Ipamorelin 3mg Lot# SIP210; Exp: 12/15/2021
Lot# SIP215; Exp: 01/14/2022
Lot# SIP220; Exp: 01/23/2022

AOD-9604 3mg Lot# AOD205; Exp: 11/09/2021
Lot# AOD210; Exp: 11/18/2021
Lot# AOD 215; Exp: 12/15/2021
Lot# AOD202; Exp: 11/09/2021

Check the full recall details on fda.gov

Source: FDA
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July 12, 2021 2:22 PM

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July 23, 2021 12:03 AM

“Company name: HIS
Brand name: HIS
Product recalled: Dietary Supplement for Weight Loss
Reason of the recall: Undeclared Sibutramine
FDA Recall date: July 22, 2021
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Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues. The presence of sibutramine in Miss Slim renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. To date, HIS has not received any reports of adverse events related to this recall.

The product is marketed as a dietary supplement and is packaged 10 count UPC (742137605030) and 30 count UPC (609728434472) capsules. The product sold online at missslimusa.com.

Risk Statement: Products containing sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

HIS is notifying its customers by website missslimusa.com and is arranging for return of all recalled products. Consumers that have Miss Slim which is being recalled should stop using it. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Check the full recall details on fda.gov

Source: FDA
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July 14, 2021 9:01 PM

“Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
Product recalled: Sunscreen
Reason of the recall: Testing identified low levels of benzene
FDA Recall date: July 14, 2021
Recall details: Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen... See More product lines to the consumer level. Internal testing identified low levels of benzene in some samples of the products. Consumers should stop using the affected products and follow the instructions set forth below.

The only sunscreen products impacted are aerosol products, specifically: NEUTROGENA® Beach Defense® aerosol sunscreen:
- NEUTROGENA® Cool Dry Sport aerosol sunscreen
- NEUTROGENA® Invisible Daily™ defense aerosol sunscreen
- NEUTROGENA® Ultra Sheer® aerosol sunscreen
- AVEENO® Protect + Refresh aerosol sunscreen

Benzene is classified as a human carcinogen, a substance that could potentially cause cancer depending on the level and extent of exposure. Benzene is ubiquitous in the environment. Humans around the world have daily exposures indoors and outdoors from multiple sources. Benzene can be absorbed, to varying degrees, by inhalation, through the skin, and orally. Based on exposure modeling and the Environmental Protection Agency’s (EPA) framework, daily exposure to benzene in these aerosol sunscreen products at the levels detected in our testing would not be expected to cause adverse health consequences. Out of an abundance of caution, we are recalling all lots of these specific aerosol sunscreen products.

While benzene is not an ingredient in any of our sunscreen products, it was detected in some samples of the impacted aerosol sunscreen finished products. We are investigating the cause of this issue, which is limited to certain aerosol sunscreen products. Sunscreen use is critical to public health. Melanoma incidences continue to increase worldwide, and the majority of cases are caused by excessive sun exposure. It is important that people everywhere continue to take appropriate sun protection measures, including the continued use of alternative sunscreen.

The recalled sunscreen products are packaged in aerosol cans. The products were distributed nationwide through a variety of retail channels.

Consumers should stop using these specific products and appropriately discard them.

Check the full recall details on fda.gov

Source: FDA
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July 6, 2021 2:14 PM

“On 5/11/21, ordered a wood cutter for final payment of 25.99.
I received some wire contraption instead. No answer to emails sent. Scam. Do not order any products from FaceBook unless you like throwing away your money. See Less
Reported By SafelyHQ.com User

July 7, 2021 11:46 AM

“Yesterday I bought and gave my dog two dream one twist dog treats. A couple hours later he was acting sick. Head down, not himself. He's a very energetic blue Lacy so this is unlike him. Yesterday evening I noticed he was trying to poo but couldn't.... See More He refused his normal treats (not the dream bone but he gets blue buffalo bits after potty breaks) this was another red flag . My boy never turns down a treat.
All last night he was restless. It's now 10 am on the day after giving him the dream bone twists. He's still restless, can't get comfy, lays down then stands up then sits down with his head down. Won't eat, even things he normally loves. I've rubbed his belly and tried to comfort him. I let him out and walked him around a bit to try and help his bowels move along. Still nothing. He ate a bit of grass which is normal when dogs don't feel good. A bit later he started puking a massive amount and I could see alot of undigested dream bone in it. Those dream bones are the only new thing hes had and now he's really sick. I'm scared after reading about other law suites and issues regarding this product that my dog might have obstructed bowels from eating eat. I'm watching him closely and ready to take him to the vet as soon as I see if he's going to improve after puking or not. Vet visits are really expensive and if he needs surgery or declines further I'm going to raise hell. It's not okay for money hungry corporates to line their pockets while falsely advertising its products as safe knowing dam well it's killing beloved animals. My dog deserved a treat not a fight for his life.
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Reported By SafelyHQ.com User