Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Use camera
Select from library
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!
IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)
Visit our learn pages for more helpful information or, email us: support@safelyhq.com
Goodbye! and best wishes in your recovery
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

If your report is poison related call 1-800-222-1222 for a free consultation with a live medical poisoning expert

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Sobeys Liquor Cornerstone, 1940 Strachan Rd SE, Medicine Hat, AB T1B 4K4, Canada

Total all time reports:  1
Latest report: April 14, 2020 12:00 PM
1 Employee tested positive for COVID-19, Sobeys Liquor Cornerstone, 1940 Strachan Rd SE, Medicine Hat, AB T1B 4K4, Canada

1 Employee tested positive for COVID-19

April 14, 2020 12:00 PM

“An employee at Sobeys Liquor store located on Primrose Drive in Saskatoon tested positive for COVID-19 on April 6.

Source: globalnews.ca See Less
Reported By SafelyHQ.com User

Related Reports

Covid-19 OSHA Complaint, Walmart, 863 Harvest Ln, Williston, Vermont 05495, USA

Walmart, 863 Harvest Ln, Williston, Vermont 05495, USA

August 11, 2020 12:00 PM

“Walmart Retail Store, Williston, Vermont:

Concerns over exposure to COVID-19.
Employer not allowing employees to wear facemasks while working.


Alleged Hazards: 2, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-04-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Kroger, 3408 Pemberton Square Blvd, Vicksburg, Mississippi 39180, USA

Kroger, 3408 Pemberton Square Blvd, Vicksburg, Mississippi 39180, USA

August 11, 2020 12:00 PM

“Employees in the Quick List Department are not provided soap or hand sanitizer.

Social distancing is not being practiced in the Quick List Department.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-23 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Harris Teeter, 2800 S College Rd, Wilmington, North Carolina 28412, USA

Harris Teeter, 2800 S College Rd, Wilmington, North Carolina 28412, USA

August 11, 2020 12:00 PM

“1. On or about June 21, 2020, the employer had a company come into the store and spray an unknown chemical due to their being a positive COVID-19 case. The workers spraying the chemical wore protective suits and masks and were spraying the chemical throughout the store around employees. The chemi ... See Morecal was on pallet jacks, toilets, chairs and other surfaces. Employees asked management what the chemical was and were not told of the identity. They were told that it was used in other stores and that the employer did not think it was a problem. Employees later were told that the chemical was corrosive but dissipated in three minutes. Some employees experienced sore throats and skin rashes that may have been due to exposure to the unknown chemical.

2. Employees are not aware of the employer's written hazardous communication program nor are they provided safety data sheets "SDSs" for chemicals they are exposed to in the workplace to include the unknown chemical sprayed by the company for COVID 19.

3. The back receiving area is very hot, around 97 degrees; and employees have not been provided information on signs and symptoms of heat stress; and means of preventing heat stress and other heat related illness through their heat stress prevention program.




Source: Osha.gov | Receipt Date: 2020-07-07
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Domino's Pizza, Boston Post Road, Sudbury, Massachusetts 01776, USA

Domino's Pizza, Boston Post Road, Sudbury, Massachusetts 01776, USA

August 11, 2020 12:00 PM

“Employees are not wearing face masks

Alleged Hazards: 1, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2020-07-06 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walmart, 7525 Winchester Road, Memphis, Tennessee 38125, USA

Walmart, 7525 Winchester Road, Memphis, Tennessee 38125, USA

August 11, 2020 12:00 PM

“Employees are concerned with exposure to the coronavirus (COVID-19) due to the employer's failure to adhere to OSHA/CDC recommendations to protect workers. There are no procedures in place to alert employees whom may have been exposed to the coronavirus (COVID-19) in the workplace.

Alleged Hazard ... See Mores: 1, Employees Exposed: 200
Source: Osha.gov | Receipt Date: 2020-07-13
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, US Post Office, 2451 Postal Drive, Rocky Mount, North Carolina 27804, USA

US Post Office, 2451 Postal Drive, Rocky Mount, North Carolina 27804, USA

August 11, 2020 12:00 PM

“There are employees that have COVID-19 and nothing was done to clean the building and/or educate the employees.

Alleged Hazards: 1, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2020-07-22 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Stop & Shop, 100 Division Street, Ansonia, Connecticut 06401, USA

Stop & Shop, 100 Division Street, Ansonia, Connecticut 06401, USA

August 11, 2020 12:00 PM

“Peapod Division

1. Not all employee (delivery drivers) were placed in quarantine after co-workers tested positive for Covid-19.

2. All employees potentially exposed to coronavirus (COVID-19) when employees are required to report in as essential employees, and are not provided with products to ... See Moreclean, training and disinfect common office surfaces during the coronavirus (COVID-19) pandemic.

3. CDC guidelines such as but not limited to the Interim Guidance for Businesses and Employers to plan and respond to Coronavirus Disease 2019 (COVID-19) are not being followed and employees working while showing signs and symptoms of Coronavirus (COVID-19) are potentially exposing and infecting other working employees.





Alleged Hazards: 3, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2020-06-11
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Target, 5959 Poplar Avenue, Memphis, Tennessee 38119, USA

Target, 5959 Poplar Avenue, Memphis, Tennessee 38119, USA

August 11, 2020 12:00 PM

“1) The store is not cleaned properly after each confirmed case of COVID-19.
2) Customers are not informed when an associate tests positive for COVID-19.


Source: Osha.gov | Receipt Date: 2020-07-16 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, US Post Office Distribution Facility, Dixiana Road, West Columbia, South Carolina 29172, USA

US Post Office Distribution Facility, Dixiana Road, West Columbia, South Carolina 29172, USA

August 11, 2020 12:00 PM

“Where an employee tested positive for COVID19, management has not informed employees of the positive test and areas such as, but not limited to the APBS 2 machine area, breakroom, time clock area and women's restroom have not been sanitized.

Alleged Hazards: 1, Employees Exposed: 300
Source: O ... See Moresha.gov | Receipt Date: 2020-07-17 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Popeyes Louisiana Kitchen, 2600 West 12th Street, Erie, Pennsylvania 16505, USA

Popeyes Louisiana Kitchen, 2600 West 12th Street, Erie, Pennsylvania 16505, USA

August 11, 2020 12:00 PM

“1.) Employees are not wearing face masks or face coverings for the prevention of, and protection from, COVID-19.

Alleged Hazards: 1, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-07-29 See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

July 22, 2020 11:37 AM

“Decided to go to there The food was undercooked. See Less
Reported By SafelyHQ.com User

July 6, 2020 4:00 PM

“Company name: Baxter International Inc.
Brand name: Granules
Product recalled: Metformin Hydrochloride Extended-Release Tablets USP, 750 mg
Reason of the recall: N-Nitrosodimethylamine (NDMA)
FDA Recall date: July 06, 2020
Recall details: Company Announcement Granules Pharmaceuticals, Inc., Cha ... See Morentilly, VA is voluntarily recalling twelve (12) lots of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg, 100 and 500 count bottles within expiry to the consumer level due to the detection of NNitrosodimethylamine (NDMA) levels above the Acceptable Daily Intake Limit. Granules’ test results showed NDMA levels above the FDA acceptable limit in one (1) out of the twelve (12) batches distributed to the US market. All other batches continue to remain within the specifications. Out of abundance of caution Granules Pharmaceuticals, Inc. has decided to voluntarily recall all twelve (12) of the distributed lots within expiry of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg from the market. Granules Pharmaceuticals, Inc. has not received any reports of adverse events that have been confirmed to be directly related to this recall as of the date of this letter. Granules Metformin Hydrochloride Immediate-Release Tablets USP, 500 mg, 850 mg & 1000 mg and Metformin Hydrochloride Extended-Release Tablets USP, 500 mg are not affected by this recall. Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables. Metformin Hydrochloride Extended-Release Tablets USP, 750 mg are indicated as an adjunct to diet and exercise to improve blood sugar control in adults with type 2 diabetes mellitus. The Metformin Hydrochloride Extended-Release Tablets USP, 750 mg lots subject to the recall is identified in the table below. Metformin Hydrochloride Extended-Release Tablets USP, 750 mg
Check the full recall details on fda.gov
Source: FDA
See Less
Reported By SafelyHQ.com User

May 26, 2020 9:34 AM

“How could u serviced me raw wings to my family drying the cov 19 crises. I try go back talk to person who works there and her answer was, they are fine really disgusted by their food. how could you serve ... See Moreme and my family raw chicken wings! :( very upset See Less
Reported By SafelyHQ.com User

May 22, 2020 4:00 PM

“Company name: Acella Pharmaceuticals, LLC
Brand name: Acella
Product recalled: 30-mg, 60-mg and 90-mg NP Thyroid®
Reason of the recall: Super potency
FDA Recall date: May 22, 2020
Recall details: Company Announcement Acella Pharmaceuticals, LLC is voluntarily recalling a total of 13 lots of 30 ... See More-mg, 60-mg and 90-mg NP Thyroid® (thyroid tablets, USP) to the consumer level. The products are being recalled because our testing has found these lots to be superpotent. The product may have up to 115.0% of the labeled amount of Liothyronine (T3). Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive superpotent NP Thyroid, may experience signs and symptoms of hyperthyroidism (overactive thyroid) which include, but are not limited to, weight loss, heat intolerance, fatigue, muscle weakness, hypertension, chest pain, rapid heart rate, or heart rhythm disturbances. Pregnant women who take superpotent NP Thyroid may also experience negative maternal and fetal outcomes including miscarriage and/or impairment to fetal development. Patients should talk to their healthcare professional before they stop taking their NP Thyroid medicine. To date, Acella has received two reports of adverse events known to be related to this recall. NP Thyroid (thyroid tablets, USP) is composed of levothyroxine and liothyronine, and used to treat hypothyroidism (underactive thyroid). The products subject to recall are packed in 100-count bottles. See product images. To best identify the product, the NDC’s, Product Description, Lot Numbers and Expiration Dates are listed. These lots were distributed nationwide in the USA to Acella’s direct accounts.
Check the full recall details on fda.gov
Source: FDA
See Less
Reported By SafelyHQ.com User

July 20, 2020 11:39 AM

“So my girlfriend has just bitten into raw chicken there
We were told it’s not raw because it’s been temperature checked 👀

Do you guys think it looks raw? See Less
Reported By SafelyHQ.com User

June 15, 2020 10:35 PM

“My sister got a raw burger today, and was given a "free meal coupon" when she called to complain. You think she wants to go back? This was inedible. She didn't finish it, so I don't know if it would hav ... See Moree made her sick. See Less
Reported By SafelyHQ.com User

June 10, 2020 7:52 PM

“Peaceful Black Lives Matter protest through brooklyn on bikes See Less
Reported By SafelyHQ.com User

July 2, 2020 9:00 PM

“Company name: Transliquid Technologies LLC
Brand name: Mystic Shield
Product recalled: Mystic Shield Protection Topical Solution
Reason of the recall: Undeclared methanol
FDA Recall date: July 02, 2020
Recall details: Company Announcement Transliquid Technologies LLC is voluntarily recalling al ... See Morel Mystic Shield Protection Topical Solution, manufactured by Mystic Intl S.A. de C.V in Mexico City, and packaged in an 8.45 ounce (250 ml) bottles, to the consumer level. The firm’s independent testing found the products contain undeclared methanol. Risk Statement: Substantial methanol exposure “could 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 these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.”

To date, Transliquid Technologies LLC has not received any reports of adverse events related to the product in question. The product is an alcohol-based hand sanitizer used to reduce bacteria that potentially cause disease when soap and water are not available and is packaged in an 8.45 ounce (250 ml) blue or green labeled bottle with a white or transparent cap and bears a green or blue label identifying Mystic Shield Protection. The product was distributed between May 21, 2020-June 30, 2020 to select wholesale and retail customers in California, Louisiana, Massachusetts, and Texas.

Transliquid Technologies LLC has accounted for and prevented distribution of a substantial majority of the product at the consumer level and is arranging for its return. Transliquid Technologies LLC is notifying its distributors and customers by email and first-class U.S. Mail and is arranging for the return of all recalled products. Consumers, distributors, and retailers that have Mystic Shield Protection hand sanitizer, which is being recalled, should stop using and return 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 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
Reported By SafelyHQ.com User

August 1, 2020 5:01 PM

“Company name: Laboratorios Jaloma S.A. de C.V.
Brand name: Jaloma
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: August 01, 2020
Recall details: LABORATORIOS JALOMA S.A. de C.V. is voluntarily recalling all lots and all bottle sizes of the Jaloma An ... See Moretiseptic Hand Sanitizer, Ethyl Alcohol 62% With vitamin E to the consumer level. This recall has been initiated because FDA sampled the 500 mL product and found it to be contaminated with undeclared methanol (wood alcohol). Although the contamination was linked to the 500 mL product, due to the abundance of caution, Jaloma is recalling all lots of all sizes within expiry. The NDCs, lot #s, and expiration dates are listed in the table below.

Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, and 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 these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, LABORATORIOS JALOMA S.A. de C.V. has not received any reports of adverse events related to this recall.

Recalled Products:

-Product(s): Jaloma Antiseptic Hand Sanitizer Ethyl Alcohol 62% With vitamin E
-NDCs: 65055-600-02
-Sizes: 16.9 fl oz. (1.06 pt) (500 mL)
-UPC: 7 59684 51503 3
-Lot #s & Expiration Dates: 0005295 Exp: April, 2022 / 0006373 Exp: May, 2022

-Product(s): Jaloma Antiseptic Hand Sanitizer Ethyl Alcohol 62% With vitamin E
-NDCs: 65055-600-01
-Sizes: 4 fl oz (120 mL)
-UPC: 7 59684 51502 6
-Lot #s & Expiration Dates: 0005412 Exp: April, 2022 / 0007134 Exp: May, 2022 / 0007834
-Exp: May, 2022 / 0009239 Exp: June, 2022

The product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The products are distributed in a 4 fl oz (120 mL) Polyethylene Terephthalate (PET) plastic bottle and a 16.9 fl oz (1.06 pt) (500 mL) PET or High-density polyethylene (HDPE) plastic bottle. Product is labeled with a red logo with the word Jaloma written in white letters. The product was distributed throughout the United States. It was imported to one (1) wholesaler and two (2) distributors.

Each product contains a lot number and expiration date stamped directly on the bottle or on the label of the 16.9 fl oz HDPE bottle in the format below. See table for lot numbers of each individual bottle.

0007834 EXP0522

LABORATORIOS JALOMA S.A. de C.V. is notifying its customers/distributors by recall letter and consumers via this press release. LABORATORIOS JALOMA S.A. de C.V.is arranging for return and refund of all recalled products.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

July 31, 2020 10:01 PM

“Company name: Albek de Mexico S.A. de C.V
Brand name: Nuuxsan, Modesa, Assured, more
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: July 31, 2020
Recall details: Albek de Mexico S.A. de C.V is voluntarily recalling all lots and all brands of hand sa ... See Morenitizer currently in US distribution to the consumer level. This recall is being initiated out of an abundance of caution due to detection of methanol in hand sanitizer samples manufactured by Albek when product was presented for import into the United States. Risk Statement: Substantial methanol exposure could result in serious health effects (including nausea, diarrhea, vomiting, severe abdominal pain, headache, blurred vision, permanent blindness, seizures, coma, nervous system damage) or death. Persons using methanol-based products on their hands may be at risk. Young children who accidently ingest them and adolescents and adults who drink such products are most at risk for methanol poisoning. To date, there have been no reports of serious adverse events related to the products in the scope of this recall. The products are labeled for use as a hand sanitizer (or “antiseptic”) and are packaged for several nationwide distributors in a variety of formats as you can see in the link below.

The products were distributed nationwide in the United States beginning on November, 15 2019.

Albek is partnering with its distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled products. Consumers, distributors, and retailers that have product which is being recalled should stop use or distribution and return to place of purchase.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User