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Minnesota, United States

Updated: April 13, 2021 7:06 PM

Pfizer Vaccine, Shakopee, MN, USA

Symptoms: Nausea Fatigue Soreness
Shakopee, MN, USA

April 13, 2021 7:06 PM

“Just got my 2nd Pfizer vaccine. I am 34 weeks pregnant and i am experiencing a sore arm, slight nausea and fatigue. My 1st dose, i had a sore arm and fatigue. See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Everlight Solar Construction, 7515 5th Ave, MINNEAPOLIS, MN, 55423, USA

Everlight Solar Construction, 7515 5th Ave, MINNEAPOLIS, MN, 55423, USA

April 7, 2021 12:00 PM

“1. Employees are utilizing the wrong types of ladder for electrical work, i.e. aluminum ladders are being used. 2. Employees on the job site(s) are not properly trained to perform live electrical work. 3. The employer does not provide employees with any personal protective equipment for live electri... See Morecal work. 4. The employer does not provide employees with any personal protective equipment for job tasks, i.e. safety glasses or hearing protection. 5. The employer does not have or does not follow their Covid-19 Preparedness Plan: i.e. no face coverings worn by employees at all times, no social distancing, no cleaning/disinfecting performed, no plan to identify sick workers and ensure sick workers stay home.


Source: Osha.gov | Receipt Date: 2021-03-18
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Wright County-Health and Human Services, 1004 Commercial Dr, BUFFALO, MN, 55313, USA

Wright County-Health and Human Services, 1004 Commercial Dr, BUFFALO, MN, 55313, USA

April 7, 2021 12:00 PM

“Employer requiring employees to work away from home during the Governor's Stay at Home Order and having them in close contact with other employees not wearing masks for more than 15 minutes a day.


Source: Osha.gov | Receipt Date: 2021-03-17 See Less
Reported By SafelyHQ.com User
Vaccine Side Effects Special summary

Covid-19 OSHA Complaint, 3M Cottage Grove Center, 10746 Innovation Road, COTTAGE GROVE, MN, 55016, USA

3M Cottage Grove Center, 10746 Innovation Road, COTTAGE GROVE, MN, 55016, USA

April 7, 2021 12:00 PM

“1. The employees are not being furnished the proper respirators for from COVID-19, or other chemical dust/materials such as the followings: lithium salt dust, glass bubble dust, ceramic dust, aluminum powder, graphite, glassfrit/powder dust, and many other chemical powders. 2. Employees are only pro... See Morevided a dust respirator with two straps. 3. Employees are having to store contaminated respirator masks improperly. They are required to store the respirator in a bag for 14 days and then reuse.


Source: Osha.gov | Receipt Date: 2021-03-17
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Aurora On France, 6500 France Avenue S, MINNEAPOLIS, MN, 55435, USA

Aurora On France, 6500 France Avenue S, MINNEAPOLIS, MN, 55435, USA

April 7, 2021 12:00 PM

“The employer is not following safety standards and COVID-19 Guidelines for the following items: 1. Emergency exit routes are blocked to do an excessive number of carts being stored in the walkways. 2. Trays come back with towels and other materials contaminated with blood. 3. Employees not informed... See Moreof which residents have COVID-19 or suspected to have COVID-19 so precautions can be taken when delivering and picking up meal trays in the resident's rooms. 4. Possibility of handling trays that have been contaminated with COVID-19 germs without the proper precautions not being taken. 5. Trays or other items wrapped in plastic bags are being sent back to the kitchen for cleaning and employees are not informed of the hazards.


Source: Osha.gov | Receipt Date: 2021-03-16
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, St Paul Public Schools Bus Transportation, 261 Chester St, SAINT PAUL, MN, 55107, USA

St Paul Public Schools Bus Transportation, 261 Chester St, SAINT PAUL, MN, 55107, USA

April 7, 2021 12:00 PM

“Employees exposed to a chemical, Dynom All-purpose Foaming germicide, utilized to clean the bus seats multiple times a day as a Covid sanitizer.


Source: Osha.gov | Receipt Date: 2021-03-12 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Applebees, 14678 Cedar Ave, SAINT PAUL, MN, 55124, USA

Applebees, 14678 Cedar Ave, SAINT PAUL, MN, 55124, USA

April 7, 2021 12:00 PM

“1. No Covid-19 preparedness plan in place or being used. 2. The employer is not notifying employees who have been exposed to other employees who have tested positive for COVID-19.


Source: Osha.gov | Receipt Date: 2021-03-05 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, MN Dept of Corrections - St Cloud, 2305 Minnesota Blvd SE, SAINT CLOUD, MN, 56302, USA

MN Dept of Corrections - St Cloud, 2305 Minnesota Blvd SE, SAINT CLOUD, MN, 56302, USA

April 7, 2021 12:00 PM

“1. The employer has not provided medical evaluations or training as specified in the Respiratory Protection Standard (29 CFR 1910.134) for employees required to wear N95 respirators due to COVID-19 activity at the facility. 2. Employees required to wear respirators have not been fit tested for all m... See Moreakes and models of N95 respirators being provided for use by the employer.


Source: Osha.gov | Receipt Date: 2021-02-24
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Reported By SafelyHQ.com User

Second Covid vaccination side effects, Minneapolis, MN, USA

Symptoms: Diarrhea Fever Headache Dizziness Fatigue Body Ache
Minneapolis, MN, USA

April 3, 2021 9:49 AM

“Second Pfizer Bio n Tech vaccine side effects laid me up in bed for well over 60 hours...Horribly sick...aches, headache,dizzy, fever of 100.5 which dropped down to 99.5 48 hours later. Normal today at 72 hours afterwards. First I could eat in 72 hours - chicken noodle soup. If I had to do it again,... See Morenot sure I would. Warning people to plan on missing ONE day of work? More likely 2 days of work. Last symptom was diarrhea...never made it to the toilet. The side effects are an ordeal. See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Allstar Childcare Center, 980 10th Street NE, MILACA, MN, 56353, USA

Allstar Childcare Center, 980 10th Street NE, MILACA, MN, 56353, USA

April 1, 2021 12:00 PM

“1. Employees not wearing masks indoors. 2. Employer not informing employees when they are exposed to Covid positive individuals.


Source: Osha.gov | Receipt Date: 2021-03-16 See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

March 26, 2021 7:00 PM

“Company name: Namoo Enterprise LLC
Brand name: PremierZen
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 26, 2021
Recall details: Little Ferry, NJ, Namoo Enterprise LLC is voluntarily recalling al... See Morel lots within expiry of PremierZen Black 5000 capsules to the consumer level. FDA analysis has found the product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil, known as phosphodiesterase (PDE-5) inhibitors, are found in FDA approved products for the treatment of male erectile dysfunction.

The presence of sildenafil and tadalafil in PremierZen Black 5000 products makes them unapproved new drugs for which the safety and efficacy have not been established and therefore subject to recall. Risk Statement: Consumers with underlying medical issues who take PremierZen Black 5000 with undeclared sildenafil and tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates.

To date, Namoo Enterprise LLC has not received any reports of adverse events related to this recall. The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in card form with one capsule per card and is aware of at least one lot with an expiration date of December 2023. Each pack is black with gold, blue, white and red text. The capsule appears black and is enclosed within clear plastic on the package. The affected lots of PremierZen Black 5000 includes all lots. PremierZen Black 5000 was sold nationwide in the USA via the internet and fulfilled by ebay at www.ebay.com and also fulfilled by amazon at www.amazon.com.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms. Namoo Enterprise LLC is notifying its customers by this press announcement and by mailing recall letters. Consumers that have PremierZen Black 5000 should stop using and destroy them. Consumers with questions regarding this recall can contact Namoo Enterprise LLC by phone at 201-267-0539, Monday to Friday, 9 A.M. to 5 P.M. EST or email at namooenterprise@gmail.com from Monday to Friday.

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. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

March 24, 2021 4:00 PM

“Company name: Alembic Pharmaceuticals, Inc.
Brand name: Alembic
Product recalled: Telmisartan Tablets, USP, 20 mg
Reason of the recall: Incorrect Product Strength on Label
FDA Recall date: March 24, 2021
Recall details: Bridgewater, NJ, Alembic Pharmaceuticals, Inc is voluntarily recalling on... See Moree lot of Telmisartan Tablets, USP, 20 mg, packaged in 30-count bottles, Lot No. 1905005661 to the consumer level. The product is being recalled due to a market complaint received which stated that one bottle labelled as 30-count Telmisartan Tablets, USP, 20 mg incorrectly contained 30 tablets of Telmisartan Tablets, USP, 40mg.

Risk Statement: Patients who could be on a doubled dose of telmisartan for a prolonged period of time, could experience low blood pressure, worsening of kidney function, or an elevation of potassium which can be life-threatening. To date, Alembic Pharmaceuticals Limited has not received any reports of adverse events related to this recall. The product is used for the treatment of hypertension i.e. to lower blood pressure and is packaged in a bottle of 30 tablets having NDC Number 62332-087-30.

The affected lot of Telmisartan Tablets, USP, 20 mg is the lot number 1905005661 and the lot expires in March 2022. The wrong product can be identified by checking the shape and embossing details on the tablets i.e. Telmisartan Tablets, USP, 20 mg bottles may incorrectly contain oval shaped White to off-white tablets debossed with L203 on one side instead of correct product i.e. round shaped White to off-white tablets debossed with L 202 on one side. Telmisartan Tablets, USP, 20mg, Lot No. 1905005661 was distributed Nationwide in the USA to wholesalers, retailers, and pharmacies.

Alembic Pharmaceuticals Limited is notifying its distributors and retailers through letter and is arranging for return of the recalled lot. Consumers that may have Telmisartan Tablets, USP, 20 mg which is being recalled should not discontinue use until speaking with their pharmacist or healthcare professional for a replacement before returning to place of purchase. Consumers with questions regarding this recall can contact Alembic Pharmaceuticals Inc by phone at +1 908-552-5839 (9:00 am – 5:00 pm, EDT, Monday through Friday) or email address david.cobb@alembicusa.com.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

April 4, 2021 6:56 PM

“The CDC announced that they are currently investigating a multistate outbreak of Salmonella infections where 19 people have been reported sick from 8 states (CA, KY, MS, NH, OK, OR, TN, WA). Eight people of the total have required hospitalization but no deaths have been reported to date.

Accordin... See Moreg to the outbreak notice, there are reports of wild songbirds, such as pine siskins (small, streaked, yellow-tinged songbirds in the finch family) sick with the same strain of Salmonella that is making people sick in this outbreak. Salmonella germs can spread between species of birds, to pets, and to people.

You can get sick when you touch your mouth with unwashed hands after touching wild birds, bird feeders or bird baths, or your pets that have contact with wild birds.

CDC advises to:
- Clean and disinfect your bird feeder and bird bath weekly or when they are visibly dirty.
- Do not touch or hand-feed wild birds with your bare hands.
- Always wash your hands with soap and water
- Call your healthcare provider right away if you have any of these severe Salmonella symptoms

Most people infected with Salmonella develop diarrhea, fever, and stomach cramps 6 hours to 6 days after being exposed to the bacteria and the illness usually lasts 4 to 7 days, and many recover without treatment.

Check the CDC website for the full investigation details cdc.gov

Source: CDC
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Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Salmonella
Vaccine Side Effects Special summary

April 7, 2021 11:00 AM

“Company name: Yolo Studio
Brand name: PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: April 06, 2021
Recall details: Cliffside Park, NJ, Yol... See Moreo Studio is voluntarily recalling all lots of PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 to the consumer level. FDA analysis has found the product to contain undeclared tadalafil. Tadalafil is ingredient known as a phosphodiesterase (PDE-5) inhibitor found in FDA approved products for the treatment of male erectile dysfunction.

The presence of tadalafil in PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 makes these unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall. Consumers with underlying medical issues who take PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 with undeclared tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening.

Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, Yolo Studio has not received any reports of adverse events related to this recall. These tainted products are marketed as dietary supplements for male sexual enhancement and are packaged in cardboard blisters containing one pill per card.

The affected lot numbers of PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 include all lots. PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 were distributed via internet and fulfilled by amazon at www.amazon.com nationwide in the USA. On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients.

It also encouraged online marketplaces to ensure these products are not sold on their platforms. Yolo Studio is notifying its customers by this press announcement and via e-mail of this recall. Consumers that have PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 which are being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Yolo Studio by phone at (201) 233-3521 Monday through Friday from 9am to 5pm eastern time zone or e-mail yolostudiodamazon@gmail.com.

Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to taking or using these drug products. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Pfizer First Dose Vaccine, Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

Symptoms: Headache Fatigue Soreness
Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

April 2, 2021 7:33 PM

“The vaccine process went relatively smooth. Waited the recommended 15 minutes for any allergic reactions. Had none. My side effects have been mild. Headache, run down feeling, head fogginess, sore arm from where the vaccine was injected, alittle fatigued, and have noticed my heart rate being alittle... See Moretoo high for comfort. See Less
Reported By SafelyHQ.com User

April 5, 2021 5:00 PM

“Company name: QMART
Brand name: IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and/or Tadalafil
FDA Recall date: April 05, 2021
Recall det... See Moreails: Company Announcement Elmwood Park, NJ, QMART is voluntarily recalling all lots of IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 to the consumer level. FDA analysis has found the products to be tainted with undeclared sildenafil and/or tadalafil. Sildenafil and tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction. The presence of sildenafil and/or tadalafil in IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 renders them unapproved drugs for which the safety and efficacy have not been established and, therefore, subject to recall. Risk Statement: Consumers with underlying medical issues who take IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 capsules with undeclared sildenafil and/or tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, QMART has not received any reports of adverse events related to this recall. These tainted products are marketed as dietary supplements for male sexual performance enhancement and are packaged in cardboard blisters. The affected lots of IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 include all lots. The product can be identified by the UPC codes in the table below which were distributed via internet and fulfilled by amazon at www.amazon.com. On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.
Check the full recall details on fda.gov
Source: FDA
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Reported By SafelyHQ.com User

Covid Vaccine AstraZeneca, Glasgow, UK

Symptoms: Skin Rash Muscle Pain
Glasgow, UK

March 29, 2021 5:06 AM

“After I have my astrazeneca vaccine I had a bad pain in my arm for 4 days but that was not the worst part, I believe the astrazeneca triggered a bad episode of eczema as my skin was fine before the vaccine but shortly after the vaccine my skin started to flair up really badly and I’ve had to go on A... See Morentibiotics. Eczema is caused by an overactive immune response, I believe the astrazeneca triggered a strong immune response and in doing so triggered a outbreak of raw, bleeding skin which became infected and couldn’t Be treated with over the counter creams. I’ve been in severe pain with it for three weeks. I don’t know if it’s a coincidence but I didn’t have any signs of eczema before hand and I was eczema free for over a year. See Less
Reported By SafelyHQ.com User

April 9, 2021 3:15 PM

“I got the j&j vac at 1:00pm its been 1 hour so far only a slight tingling on vaccination spot other than that nothing big hoping for the best See Less
Reported By SafelyHQ.com User

After first Moderna shot, Sebastopol, CA, USA

Symptoms: Other Body Ache Soreness
Sebastopol, CA, USA

March 26, 2021 5:51 PM

“Sore arm first night, much like a flu shot. In subsequent days had achy lymph nodes in armpit, neck and upper chest. No big deal, just rather odd. 9 days after shot I woke with first Atrial fib in almost 6 weeks (had second Cardiac ablation last summer that we hoped would "fix" it). I had Afib episo... See Moredes next two nights, decreasing in intensity, but certainly requiring meds and monitoring. Since been diagnosed with Afib bit over 2 years ago had never had it multiple days in a row before.
Since then, every days it's less problematic. Now just an hour of feeling a tad funky in the afternoons.Asked my cardiologist if he'd had other patients with similar reactions and he said "yes", but mostly after second vaccination. Seems as if the inflammation that's triggered by vaccine as body responds and creates antibodies to virus, triggers "twitchy" susceptible heart into freaking out (my language, not his!) Makes me rather dread how I"m going to feel next week after second shot, But will certainly not deter me to get fully covered.
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Reported By SafelyHQ.com User

Pfizer vaccine first dose, Fort Collins, CO, USA

Symptoms: Soreness
Fort Collins, CO, USA

April 13, 2021 11:07 PM

“I just received my first dose today. The shot was completely painless. I did not have any soreness in my arm until a few hours later. No side effects so far. I have been feeling good after the shot. My next one is in 21 days. See Less
Reported By SafelyHQ.com User