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Connecticut, United States
Updated: April 7, 2021 12:00 PM
Covid-19 OSHA Complaint, Arett Sales, 780 James P. Casey Road, Suite 200, BRISTOL, CT, 06010, USA
Arett Sales, 780 James P. Casey Road, Suite 200, BRISTOL, CT, 06010, USA
April 7, 2021 12:00 PM
“1. Employees who work on and around powered industrial trucks are not required to wear steel toe shoes and hard hats. 2. Protocols set by the CT Department of Public Health and the CDC are not being followed with regard to use of face coverings and self-quarantining after COVID diagnosis.
Alleged H... See Moreazards: 2, Employees Exposed: 11
Source: Osha.gov | Receipt Date: 2021-03-01 See Less”
Helpful
Covid-19 OSHA Complaint, DR. CAI EYECARE CENTER, 477 Connecticut Boulevard, EAST HARTFORD, CT, 06108, USA
DR. CAI EYECARE CENTER, 477 Connecticut Boulevard, EAST HARTFORD, CT, 06108, USA
April 7, 2021 12:00 PM
“Employees are not provided with a place of employment free from recognized hazards in that, masks are not worn and a limited number of people occupying the office and social distancing is not enforced.
Alleged Hazards: 2, Employees Exposed: 6
Source: Osha.gov | Receipt Date: 2020-12-30 See Less”
Helpful
Covid-19 OSHA Complaint, Trader Joe's East Inc., 400 Post Rd E, WESTPORT, CT, 06880, USA
Trader Joe's East Inc., 400 Post Rd E, WESTPORT, CT, 06880, USA
April 7, 2021 12:00 PM
“Since March 3, 2021 multiple workers are testing positive for COVID currently working and its now out of hand. Manager refuses to acknowledge the severity of these ongoing cases. The store is no longer safe and workers fear for their safety and health.
Alleged Hazards: 1, Employees Exposed: 30
So... See Moreurce: Osha.gov | Receipt Date: 2021-03-08 See Less”
Helpful
Covid-19 OSHA Complaint, Stop and Shop, 125 Danbury Road, RIDGEFIELD, CT, 06877, USA
Stop and Shop, 125 Danbury Road, RIDGEFIELD, CT, 06877, USA
April 7, 2021 12:00 PM
“Deli department employees are exposed to slip and trip hazards due to the placement of meat slicers and scales. Employer is not following the CDC recommended guidelines for social distancing in the deli department.
Alleged Hazards: 2, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-03... See More-05 See Less”
Helpful
Covid-19 OSHA Complaint, Raymour & Flanigan, 1799 Boston Post Road, MILFORD, CT, 06460, USA
Raymour & Flanigan, 1799 Boston Post Road, MILFORD, CT, 06460, USA
April 7, 2021 12:00 PM
“Known infected workers who have been treated and on sick leave for COVID -19 related systems, are allegedly not being quarantined and are returning to the workplace without proper notification to co-workers. In addition occupational health documentation is not being administered to certify a return... See Moreto duty status by a medical doctor. Known infected employees without return work authorization are in work functions that inherently require contact with numerous work areas and other co-workers in the retail and office workplace. The employer is not following the most current CDC Guidelines, such as, but not limited to, the supervisors, manager, staff, and customers are not properly wearing mask/face coverings throughout the reception, administrative office, retail store and the Interim Guidance for Businesses and Employers to plan and respond to the Coronavirus Disease 2019 (COVID-19) are not being followed. It is alleged the employer is not proper disinfecting and cleaning is not being performed in accordance with CDC Guidelines, especially for high touch areas for employees, due to cleaning measures that are not effective.
Alleged Hazards: 1, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2021-03-02 See Less”
Helpful
Pfizer vaccine No after effects at all - just relief that I could finally get the shot, New Haven, CT, USA
New Haven, CT, USA
April 3, 2021 12:15 PM
“I had no reaction to the vaccine. None at all, not even a sore arm and neither did my wife. No fatigue, just a feeling of relief that it was finally done. I usually get at least a sore arm from a flu shot, so this was quite a pleasant experience. See Less”
Helpful
Covid-19 OSHA Complaint, D&D Carbide Grinding, Inc, 598 Deming Rd, BERLIN, CT, 06037, USA
D&D Carbide Grinding, Inc, 598 Deming Rd, BERLIN, CT, 06037, USA
March 31, 2021 12:00 PM
“Employees are exposed to SARS-Cov-2 transmission in that, cleaning and disinfecting is not done throughout the workplace and employees are allowed to return to work after testing positive with the COVID-19 disease without confirmation that it is safe for them to return.
Alleged Hazards: 2, Employe... See Morees Exposed: 25
Source: Osha.gov | Receipt Date: 2021-03-03 See Less”
Helpful
Covid-19 OSHA Complaint, Car Parts International LLC, 221 Locust Street, HARTFORD, CT, 06114, USA
Car Parts International LLC, 221 Locust Street, HARTFORD, CT, 06114, USA
March 31, 2021 12:00 PM
“Several employees have been exposed to COVID-19. Two employees who were exposed are still working and making deliveries without having received a negative COVID-19 test, potentially exposing others to the virus.
Alleged Hazards: 1, Employees Exposed: 9
Source: Osha.gov | Receipt Date: 2021-02-13 See Less”
Helpful
Covid-19 OSHA Complaint, Sikorsky Aircraft Corporation, 6900 Main Street, STRATFORD, CT, 06614, USA
Sikorsky Aircraft Corporation, 6900 Main Street, STRATFORD, CT, 06614, USA
March 31, 2021 12:00 PM
“The employer is not enforcing the mask wearing policy for the employees and while the outside contractors are on site during the Coronavirus (COVID-19) pandemic on the manufacturing floor, hangar areas, backshops, and paintshop locations
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov |... See MoreReceipt Date: 2021-03-11 See Less”
Helpful
Covid-19 OSHA Complaint, Quality Propane, 359 East Main St., CLINTON, CT, 06413, USA
Quality Propane, 359 East Main St., CLINTON, CT, 06413, USA
March 31, 2021 12:00 PM
“1. Known infected workers who have been treated and on sick leave for COVID-19 related systems, are allegedly not being quarantined and are returning to the workplace without proper notification to co-workers. In addition, occupational health documentation is not being administered to certify a retu... See Morern to duty status by a medical doctor. 2. Known COVID-19 infected employees without return work authorization are in work functions that inherently require contact with numerous work areas and other co-workers in the retail and office workplace, potentially exposing workers to COVID-19. 3. The employer is not following the most current CDC Guidelines, such as, but not limited to, the supervisors, manager, staff, members and customers are not properly wearing mask/face coverings throughout the reception, administrative office, retail store and the Interim Guidance for Businesses and Employers to plan and respond to the Coronavirus Disease 2019 (COVID-19) are not being followed. 4. It is alleged the employer is not properly disinfecting and cleaning is not being performed in accordance with CDC Guidelines, especially for high touch areas for employees, due to cleaning measures that are not routine or effective.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-03-04 See Less”
Helpful
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 See Less”
Helpful
1 person found this review helpful
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 See Less”
Helpful
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”
Helpful
2 people found this review helpful
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. See Less”
Helpful
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”
Helpful
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. See Less”
Helpful
1 person found this review helpful
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 See Less”
Helpful
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 See Less”
Helpful
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. . See Less”
Helpful
5 people found this review helpful
Blackcass.com chainsaw, scam, Denver, CO, USA
Denver, CO, USA
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”
Helpful
1 person found this review helpful