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New Hampshire, United States

Updated: April 7, 2021 12:00 PM

Covid-19 OSHA Complaint, Marshalls of MA, Inc., 75 S. River Rd., BEDFORD, NH, 03110, USA

Marshalls of MA, Inc., 75 S. River Rd., BEDFORD, NH, 03110, USA

April 7, 2021 12:00 PM

“1. Employees are using a fungicide to clean the cash register counters and shopping carts in between each customer without adequate personal protective equipment. The label on the fungicide instructs users to wear gloves, and protective eyewear when handling.

Alleged Hazards: 1, Employees Exposed:... See More30
Source: Osha.gov | Receipt Date: 2020-11-16
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, RMHNH, LLC, 319 New Zealand Rd, SEABROOK, NH, 03874, USA

RMHNH, LLC, 319 New Zealand Rd, SEABROOK, NH, 03874, USA

March 31, 2021 12:00 PM

“The employer did not adapt infection control strategies based on a thorough hazard assessment, using appropriate combinations of engineering and administrative controls, safe work practices, and taking appropriate steps to protect other workers from exposure to SARS-CoV-2, the virus that causes COVI... See MoreD-19, in the workplace. These steps might include mandatory mask use, physical distancing or actions as a result of a confirmed case, such as cleaning and disinfecting the work environment, notifying other workers to monitor themselves for signs/symptoms of COVID-19, following quarantine guidelines or implementing a screening program in the workplace (e.g., for signs/symptoms of COVID-19 among workers).


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

Covid-19 OSHA Complaint, Krex Transport Inc., 40 Coachman Rd., WEST CHESTERFIELD, NH, 03466, USA

Krex Transport Inc., 40 Coachman Rd., WEST CHESTERFIELD, NH, 03466, USA

March 31, 2021 12:00 PM

“Employer is not enforcing the use of masks by employees.

Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-02-19 See Less
Reported By SafelyHQ.com User
Vaccine Side Effects Special summary

Covid-19 OSHA Complaint, All Brite Cleaning & Restoration, Inc., 41 County Club Road., GILFORD, NH, 03249, USA

All Brite Cleaning & Restoration, Inc., 41 County Club Road., GILFORD, NH, 03249, USA

March 31, 2021 12:00 PM

“1. Employer is not providing the proper PPE for Covid-19 sanitations, mold remediation and sewage cleanup. 2. Employer is not providing respirators or fit testing for technicians that need them.

Alleged Hazards: 2, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2021-02-01 See Less
Reported By SafelyHQ.com User

Moderna Vaccine, Whitefield, NH, USA

Symptoms: Chills Soreness
Whitefield, NH, USA

March 27, 2021 6:52 PM

“I had no reaction to either shot. The evening after the second shot my husband got chills. He took Tylenol and was mostly better the next day. Still a little bit of chills. Shoulder was sore also. See Less
Reported By SafelyHQ.com User

Moderna vaccine 1st dose, Dover, NH, USA

Symptoms: Diarrhea Headache Fatigue Stomach Pain
Dover, NH, USA

March 26, 2021 8:39 PM

“Moderna vaccine 1st dose. Headache, fatigue, diarrhea and stomachache for 2 days. See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Lowe's Home Centers Inc. #2617, 90 Fort Eddy Rd., CONCORD, NH, 03301, USA

Lowe's Home Centers Inc. #2617, 90 Fort Eddy Rd., CONCORD, NH, 03301, USA

March 24, 2021 12:00 PM

“The employer does not have an adequate program in place to protect employees from COVID-19 and/or outbreaks. Mouse infestation where mice are in employees lockers, breakroom, in section where birdseed is stored, and at register area. Bathrooms are not being maintained and kept sanitary for employee... See Moreuse.

Alleged Hazards: 3, Employees Exposed: 50
Source: Osha.gov | Receipt Date: 2021-02-18
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, K.W. Thompson Tool Co. Inc, 41 Old Dover Road, ROCHESTER, NH, 03867, USA

K.W. Thompson Tool Co. Inc, 41 Old Dover Road, ROCHESTER, NH, 03867, USA

March 24, 2021 12:00 PM

“Employer does not have adequate program in place to protect employees from covid-19 exposure and/or outbreaks. Employees are not being temperature checked as the employers program states it will, employees exposed to confirmed cases are encouraged to continue going to work, and there are now 7 activ... See Moree cases at the facility.


Source: Osha.gov | Receipt Date: 2021-02-18
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Dollar Tree Stores, Inc, 103 Quality Drive, HOOKSETT, NH, 03106, USA

Dollar Tree Stores, Inc, 103 Quality Drive, HOOKSETT, NH, 03106, USA

March 24, 2021 12:00 PM

“1. The employer is not following OSHA and CDC guidelines for protecting employees during the covid-19 pandemic, including: -The employer is not assessing whether or not employees are experiencing any symptoms associated with Covid-19 prior to beginning work. -The employer is not following quarantine... See Moreguidelines for employees who are primary contacts with Covid-19 positive persons. -The flat surfaces and common touch points in the store are not sanitized regularly.

Alleged Hazards: 3, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-02-08
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Reported By SafelyHQ.com User

Pfizer Covid-19 Vaccine - First Dose, Loudon, NH, USA

Symptoms: Other Soreness
Loudon, NH, USA

March 19, 2021 3:52 PM

“The vaccine spot was in Laconia, We went the earliest morning slot I could (3-15-21) and it wasn't busy at all since they don't have a drive thru option. The process was easy and simple. Getting the shot, I didn't feel needle going in or feel the coldness of the shot like I do with flu shots. A few... See Moreseconds after injected, I felt my arm stiff but not sore or in pain. I took Tylenol as soon as I got back into the car. Around 30 mins later I felt my arm feel a burn like sting sensation and it went away within an hour. I took a muscle relaxer as well when I got home and within few hours I fell asleep. Woke back up 3 hours later and my arm was a little sore. (Flu shots make my arm feel like someone punched it and lasts for whole day and Pfizer didn't feel anything close to that) Pfizer first dose was pretty mild. My mom who is 59 years old, got the Pfizer shot with me at the same time, and her symptoms were different than mine. When she got it and after injected she didn't feel anything. About 15 mins later she feels her arm stiff and sore. She also took Tylenol as soon as she got into the car. She got home and few hours goes by she falls asleep, her arm is hurting her more. On (3-16-21) she was really tired just couldn't stay awake and her arm was still really sore. On (3-17-21) She was still sleepy and she couldn't move her arm at times where she was still sore. On (3-18-21) her arm was still sore but not as sore as it was for those last couple of days, it was pretty mild and wasn't so tired anymore. On (3-19-21) She feels 100% better today. See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

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

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

Pfizer vaccine 1st dose, CVS, Bagdad Road, Cedar Park, TX, USA

Symptoms: Soreness
CVS, Bagdad Road, Cedar Park, TX, USA

March 22, 2021 9:18 AM

“Arrived on time, just 4 people ahead of me, the line moved fast. I was out in about 20 minutes. They were well organized. It is now around 15 hours later and zero side effects, apart from some soreness at the injection site, similar to a flu shot. See Less
Reported By SafelyHQ.com User
Vaccine Side Effects Special summary

J&J vaccine, Raleigh, NC, USA

Symptoms: Fever Itching
Raleigh, NC, USA

March 29, 2021 9:50 PM

“My wife and I wanted to get the CoV2 vaccine but had significant concerns about the messenger RNA versions.
Anyway, we got the J&J vaccine, and we are satisfied with it.

However, some things need to be stated. My wife had a 103.3-degree fever the night of her shot. I didn't feel great, but the... See Moreaftereffects took longer to present themselves. While I had a slight fever, my response presented itself as bruises that itched terribly.

We are two weeks out from the vaccine, and things are going back to normal. My wife and I had to build up our stamina from the day of the shot and now (two weeks and four days ago).

Overall, we still feel that the J&J jab was the best vaccine for us. Even though this vaccine's efficacy looks less than the others, it is quite comparable if you look at the places it was tested and when it was tested.

We would highly recommend this vaccine to all who would prefer a more conventional vaccine.
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Reported By SafelyHQ.com User

Johnson and Johnson Vaccine Review, Perth Amboy, NJ, USA

Symptoms: Soreness
Perth Amboy, NJ, USA

April 6, 2021 10:19 PM

“Got the JnJ vaccine Monday morning 4/5/21 at Wegman’s Bridgewater. Other than my arm being a little sore I have no side effects at all. No head aches, no fevers, nothing! SIDE NOTE: I took a COVID test a few days before to confirm I was COVID free before getting vaccinated. I was on Claritin from th... See Moree night before because allergy season has officially started. I didn’t want the Moderna or Pfizer... not a fan of the lipid MRNA. - Stay Safe guys! 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

March 31, 2021 12:02 PM

“Company name: Nuri Trading LLC
Brand name: Thumbs Up 7, Shogun-X, 69MODE
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil, Tadalafil, Vardenafil
FDA Recall date: March 31, 2021
Recall details: Nuri Trading is voluntarily recalling all... See Morelots within expiry of Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, and 69MODE Blue 69 capsules to the consumer level. FDA analyses have found these products to contain undeclared tadalafil, sildenafil, and/or vardenafil. Sildenafil,tadalafil, and vardenafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction.

The presence of sildenafil, tadalafil, and/ or vardenafil in Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, and 69MODE Blue 69 capsules make them 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 Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69 capsules with undeclared sildenafil,tadalafil, and/or vardenafil 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, Nuri Trading 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 blister foil sheets in a box. Each box contains 10 capsules. These products 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.

Nuri Trading LLC is notifying its customers by this press announcement and via email of this recall. Consumers that have Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69, which are being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Nuri Trading by phone at (201) 380-1046 Monday to Friday from 9AM to 5PM eastern time or e-mail nuritrading17@gmail.com. For more information, please visit www.nuritradingusa.com.

Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to takin 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

April 6, 2021 5:00 PM

“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: Company Announcement Cli... See Moreffside Park, NJ, Yolo Studio is voluntarily recalling all lots of PremierZEN Extreme 3000, PremierZEN Plus 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 Plus 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 Plus 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 Plus 5000, & Triple SupremeZEN Plus 3500 include all lots. PremierZEN Extreme 3000, PremierZEN Plus 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 Plus 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. 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.

- Complete and submit the report Online.
- Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
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

I am reporting Pfizer vaccine, Lecompte, LA 71346, USA

Symptoms: Other Headache
Lecompte, LA 71346, USA

March 22, 2021 7:48 PM

“In February I received my 1st dose of Pfizer vaccine and I did get a headache.. yet it was the second dose on March 3 that made me go to the doctor and found that that vaccine has cause me to have high high blood pressure! My numbers doubled and I have not recovered. Now on high blood pressure me... See Moreds. The doctor says I have fluid built up around my heart and palpitations that are driving me to unhappy days.
Letting you know. .
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Reported By SafelyHQ.com User

March 23, 2021 5:59 PM

“All I received was the chain and straps not the chain saw how can I get my money back? I am 73 and got cheated out of $29.99 plus tax for a chain saw when all I received was a chain and I want my money back See Less
Reported By SafelyHQ.com User