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Williamsburg, Virginia, United States

Updated: June 10, 2021 10:20 AM

June 10, 2021 10:20 AM

“My story is much the same as everyone else's....On May 11 I ordered a battery powered hand held wood cutter/chainsaw. Paid $25.99 via pay pal. Waited 3 weeks and got a survival chain in the mail. I emailed the "company" and they told me that the chain IS what I ordered and that the battery powered o... See Morene is $80.
You can clearly see from the order confirmation that it tells you that you are ordering the battery powered hand held wood cutter...
These people are a scam and need to be held accountable and shut down.
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, The Pavilion at Williamsburg Place, 5483 Mooretown Rd., WILLIAMSBURG, VA, 23188, USA

The Pavilion at Williamsburg Place, 5483 Mooretown Rd., WILLIAMSBURG, VA, 23188, USA

March 31, 2021 12:00 PM

“1. Throughout the various units, residents/patients who have tested positive for COVID-19 are allowed out of quarantine into day rooms/general areas exposing staff/employees and other residents/patients to the SARS-CoV-2 virus. Examples include: Approximately two weeks ago, a COVID-19 positive resid... See Moreent/patient in room #101 of Magnolia was allowed into the day room/general areas and exposed employees who later tested positive for COVID-19. 2. Employees who have close contact with COVID-19 positive employees are not provided N95 or equivalent respiratory protection. 3. Personal protective equipment (PPE) such as gowns are not being disposed of properly. Employees required to enter COVID-19 positive resident/patient rooms are required to don gowns and other PPE upon entry and doff the PPE upon existing; however, employees are exiting the quarantined room with the PPE on and disposing the PPE in various locations to include day room/general areas. 4. Temperature checks and screening for day and night shift is not longer being conducted upon entry into the building. 5. The employer is not following (implementing) their own COVID-19 response and protection plan. Management, supervisors, and staff have become complacent.


Source: Osha.gov | Receipt Date: 2021-03-02
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Edgeworth Park at New Town, 5501 Discovery Park Boulevard, WILLIAMSBURG, VA, 23188, USA

Edgeworth Park at New Town, 5501 Discovery Park Boulevard, WILLIAMSBURG, VA, 23188, USA

January 21, 2021 12:00 PM

“1. During a COVID-19 pandemic, the employer is allowing visitors to enter the facility without face coverings or monitoring for exposure. 2. Employees who are working with COVID-19 positive patients are not provided adequate PPE before entering the patient rooms. Employees received face shields and... See MoreN95 masks in the middle of their work shifts after working with the COVID-19 positive patients. 3. PPE is not readily available as it is locked up. 4. The employer is not taking steps to isolate COVID-19 positive patients in an effort to reduce the spread/outbreak in the facility.

Alleged Hazards: 4, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-12-17
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, The Farley Center, 5477 Mooretown Rd., WILLIAMSBURG, VA, 23188, USA

The Farley Center, 5477 Mooretown Rd., WILLIAMSBURG, VA, 23188, USA

January 21, 2021 12:00 PM

“The employer has not implemented measures in the workplace to protect employees from contracting or spreading COVID-19 in the workplace. 1. The use of face coverings by employees and clients are not required or enforced. Group sessions are held in small group settings where the employees and clients... See Moreare not abiding by social distancing and are not wearing face coverings. 2. The employer is providing hand sanitizer that does not contain alcohol or is approved on the EPA list. 3. Frequently touched surfaces, to include phones, are not frequently cleaned or sanitized. 4. The employer has not implemented measures to reduce the spread of COVID-19 from clients who enter The Big House.

Alleged Hazards: 4, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-12-15
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Prism Contractors and Engineers, Inc., 1568 Manufacture Drive, WILLIAMSBURG, VA, 23185, USA

Prism Contractors and Engineers, Inc., 1568 Manufacture Drive, WILLIAMSBURG, VA, 23185, USA

December 15, 2020 12:00 PM

“Located in the shop, the company did not notify employees that someone tested positive for Coronavirus until a few days later.

Alleged Hazards: 1, Employees Exposed: 2
Source: Osha.gov | Receipt Date: 2020-11-18 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, SI Dance, LLC, 144 Tewning Road, WILLIAMSBURG, VA, 23188, USA

SI Dance, LLC, 144 Tewning Road, WILLIAMSBURG, VA, 23188, USA

December 8, 2020 12:00 PM

“The employer is not implementing precautions to protect employees from contracting and spreading the Coronavirus in the workplace, in that, 1. Patrons/students who have tested positive for the Coronavirus are allowed in the studio to dance. 2. Patrons/students who have been exposed to family members... See Morewho have tested positive are allowed in the studio to dance. 3. Employees are not notified when exposed to patrons/students who have been exposed to the Coronavirus, or have tested positive for the Coronavirus. 4. Patrons/students with fevers are allowed in the studio to dance. 5. Cleaning and disinfecting is not being conducted between dance classes. 6. Patrons/students are not wearing face coverings correctly. 7. Social distancing is not being practiced.

Alleged Hazards: 7, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-11-18
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Bluegreen Vacations Preview Center at Patrick Henry Square, 249 York St, WILLIAMSBURG, VA, 23185, USA

Bluegreen Vacations Preview Center at Patrick Henry Square, 249 York St, WILLIAMSBURG, VA, 23185, USA

November 25, 2020 12:00 PM

“1. The employer failed to notify employees within 24 hours after becoming notified of a positive COVID-19 case in the workplace. The employer waited at least three days before informing those employees who had been around the COVID-19 positive person in the establishment, and did not conduct contact... See Moretracing to determine who had been exposed. 2. After being notified of a positive COVID-19 case in the workplace, the employer did not quarantine those exposed employees. 3. The employer did not ramp up disinfecting of surfaces after having a positive COVID-19 case in the workplace.

Alleged Hazards: 3, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-09-17
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Reported By SafelyHQ.com User

Employee tested positive for Covid-19, Berkeley Middle School, 1118 Ironbound Rd, Williamsburg, VA 23188, USA

Berkeley Middle School, 1118 Ironbound Rd, Williamsburg, VA 23188, USA

September 17, 2020 12:00 PM

“A Williamsburg-James City County Schools employee at Berkeley Middle School in Williamsburg tested positive for the coronavirus

Source: wtkr.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, James City County Recreation Center, 5301 Longhill Rd, Williamsburg, VA 23188, United States

James City County Recreation Center, 5301 Longhill Rd, Williamsburg, VA 23188, United States

July 5, 2020 12:00 PM

“An employee at the James City County Recreation Center has tested positive for the virus

Source: wydaily.com See Less
Reported By SafelyHQ.com User

Jail employee tests positive for COVID -19, Virginia Peninsula Regional Jail, 9320 Merrimac Trail, Williamsburg, VA 23185, USA

Virginia Peninsula Regional Jail, 9320 Merrimac Trail, Williamsburg, VA 23185, USA

April 28, 2020 12:00 PM

“An employee at the Virginia Peninsula Regional Jail has tested positive for COVID -19

Source: wavy.com See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

May 24, 2021 1:12 PM

“I ordered 2 of the Battery Power Woodcutters.
They were advertised on Facebook.
I placed my order April25,2021. They were for bday presents in May. I ordered them using Pay Pal.
I want my money refunded within 7 days.
I wish I had read up on them and saw all the comments I never would have or... See Moredered them.
The good thing is my husband works at the Sherffi’s office and he will be looking into this
So y’all better get my refund cause if this is a scam they will know
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Reported By SafelyHQ.com User

June 5, 2021 8:25 PM

“Miss leading information on the product. Ordered battery operated power saw. like some of the other customers and I also got a wire chain with a ring on each end. This a scam..
Amphitrite. Technology Limited. I ordered a Battery Powered Wood Cutter, hand held Chainsaw. I am not the only person that... See Moregot scammed on this. See Less
Reported By SafelyHQ.com User

June 4, 2021 3:58 AM

“Bait and switch from this company. No phone number to call. Such a hassle for all of us trying to clean up from fallen trees. It is still on Instagram See Less
Reported By SafelyHQ.com User

June 2, 2021 11:43 AM

“Ordered a Mini chainsaw seen frequently on Facebook and got a small wound chain on two rings a total misrepresentation of their product..They are a total Fraud and should be shutdown . April 18 th ordered , received the pocket chain almost two months later for 27dollars and change .What a rip off. See Less
Reported By SafelyHQ.com User

May 28, 2021 6:02 PM

“Company name: Dash Xclusive
Brand name: Imperia Elita
Product recalled: Imperia Elita Vitaccino Coffee
Reason of the recall: Undeclared Sibutramine and Fluoxetine
FDA Recall date: May 28, 2021
Recall details: Dash Xclusive is voluntarily recalling all lots of Imperia Elita Vitaccino Coffee to... See Morethe consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine. Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues, including stroke, heart failure and serious health risk especially to those with underlying heart related disease.

Fluoxetine is an FDA approved drug indicated for the treatment of various depressive disorders, obsessive compulsive disorder, bulimia and panic disorders. This drug product carries a box warning for suicidal thoughts and behaviors and it needs to be monitored closely by a prescriber.

The presence of sibutramine and fluoxetine in Imperia Elita Vitaccino coffee renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. Dash Xclusive has not received any reports of adverse events related to this recall.

Risk Statement: Products containing undeclared 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.

Products containing undeclared fluoxetine could cause suicidal thinking and behavior, an accumulation of high levels of serotonin in the body or neuroleptic malignant syndrome (NMS)-like reactions which is a life-threatening neurological disorder; elevated mood state that can cause higher than normal energy levels, restlessness, decreased need for sleep; abnormal bleeding, and low sodium levels.

The product is marketed as a dietary supplement for weight loss and is packaged in a black rectangular box and contains fifteen sachets. The affected Imperia Elita Vitaccino coffee lots include all lots. Product was distributed Nationwide in the USA via internet and by ebay at www.ebay.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. Dash Xclusive is notifying its customers by e-messages on the eBay platform and is arranging for return of all recalled products. Consumers that have Imperia Elita Vitaccino Coffee which is being recalled should stop using/return to Dash Xclusive, PO BOX. #220, 1125 E. Broadway Glendale, California 91205.

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. 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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June 7, 2021 11:39 AM

“I read all these other people that never received theirs either, how do I get my refund of 28.00 from Amphitrite Techology Limited. I am reporting this because I never received my mini chain saw,I purchased from Amphitrite Techology Limited See Less
Reported By SafelyHQ.com User

Dream Bone made with peanut butter, Nashville, Arkansas, USA

Symptoms: Diarrhea
Nashville, Arkansas, USA

June 10, 2021 2:52 PM

“The Dog had runny diarrhea after eating only two. See Less
Reported By SafelyHQ.com User

May 25, 2021 4:00 PM

“Company name: Global Sanitizers
Brand name: Medically Minded
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 25, 2021
Recall details: This is to inform you of a product recall involving: Medically Minded Hand Sanitizers: 8 oz. UPC 676753004208; L... See Moreot E332020, Lot E212020, and Lot E082020 8.5 oz. UPC 676753004147; Lot E372020 10 oz. UPC 676753004178 Lot GV4420205.

This recall has been initiated due to the presence of undeclared Methanol. Use of or consumption of this product can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma & or permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

Methanol was discovered through lab testing. To date, Global Sanitizers has not received any reports of adverse events related to this recall. We began shipping this product on approximately July 10, 2020. Immediately examine your inventory and quarantine product subject to recall.

In addition, if you may have further distributed this product, please identify your customers and notify them at once of this product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter.

If you have these recalled items in stock, please send an email to recall@globalsanitizers.com and we provide further instructions for product destruction. This recall should be carried out at the consumer level. This recall is being made with the knowledge of the Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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May 17, 2021 4:00 PM

“Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Hand sanitizer
Reason of the recall: Product is contaminated with Burkholderia contaminants
FDA Recall date: May 17, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan is updating its previously anno... See Moreunced voluntary recall of Durisan Non-Alcohol Antimicrobial Hand Sanitizer products that became contaminated with a common municipal water supply-borne bacteria, Burkholderia contaminants. Use of a hand sanitizer contaminated with Burkholderia contaminants, generally considered to be of low virulence, can range from no reaction to possible infections in a person with a hand-wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems.

In the April 10, 2021 announcement, Durisan expanded the recall to include all of its Hand Sanitizer products that had not expired (produced after 4/10/2019). Durisan discovered that promotional orders, as well as small run production lot numbers which were not listed, were intended for inclusion in the recall. For clarification, in the link below are all affected lot numbers.

Customers or consumers in possession of Durisan Non Alcohol Antimicrobial Hand Sanitizer products with these numbers in any form factor are encouraged to contact Durisan. To date, no qualified reports of adverse reactions have been reported related to this recall. The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available.

The product is packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. At this time, we are including lot numbers of promotional orders, wipes, and private label products. The lot number can be found in black print on the bottom of the package. Durisan Antimicrobial Solutions hand sanitizer sizes with the identification are listed in the link below.

Durisan has provided written notification to its distributors and retailers and is alerting consumers via this voluntary recall. Consumers that have the product are advised to contact Durisan to return it. 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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May 19, 2021 1:00 PM

“Company name: Dibar Nutricional S. de R.L. de C.V.
Brand name: DIBAR Labs, ProtectoRx
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 19, 2021
Recall details: Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (“Dibar”) is voluntari... See Morely recalling all Dibar Labs Hand Sanitizer packaged in 8oz and 16 oz bottles, respectively, to the consumer level (see Label 1 below). Dibar is also voluntarily recalling ProtectoRx Hand Sanitizer packaged in 2oz and 16oz fluid ounce bottles, respectively, to the consumer level (see Label 2 below), as well as all Advance Hand Sanitizer packaged in 16 oz bottles, likewise, to the consumer level (see Label 3 below). These products are being recalled after testing conducted by our firm revealed the presence of methanol.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.

To date, the company has not received any reports of adverse reactions related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available.

The affected bottles of hand sanitizer include a twelvedigit lot code printed on the bottle near the base. The products can be identified by the label image provided at the end of this release. Products labeled as Dibar Labs Hand Sanitizer were distributed nationwide in the USA through S.E.N.D. LLC and its customers. Products labeled as ProtectoRx Hand Sanitizer were distributed in Puerto Rico through PR TRADING LLC and its customers. Products labeled as Advance Hand Sanitizer were distributed in the USA through RGV HEALTH SERVICES LLC DBA VALLEY and its customers.

Dibar Nutricional S. de R.L. De C.V., has notified its direct distributors by letter and asked that they remove the recalled products from commerce immediately if they still possess inventory.

Consumers, distributors and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this 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. Link to Original Recall

Check the full recall details on fda.gov

Source: FDA
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