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

Birds Eye, W8880 Co Rd X, Darien, WI 53114, USA

Total all time reports:  1
Latest report: April 23, 2020 12:00 PM
20 employees testing positive for COVID-19,, Birds Eye, W8880 Co Rd X, Darien, WI 53114, USA

20 employees testing positive for COVID-19,

April 23, 2020 12:00 PM

“20 employees at the Birds Eye food processing plant in Darien have tested positive for COVID-19.

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

Related Reports

9 Covid cases, Houlihan's, West 95th Street, Overland Park, KS, USA

Houlihan's, West 95th Street, Overland Park, KS, USA

August 4, 2020 7:25 PM

“There have been at least 9 positive cases among employees but the restaurant has not shut down, does not notify other employees, and has not required employees to get tested See Less
Reported By SafelyHQ.com User

August 4, 2020 4:44 PM

“Graybar in Pomona Ca had an employee test positive for corona Virus. Employer didn't inform staff till there shift was over. Staff was inform to come back to work the next day at 4am. When staff returned there was no sign of cleaning or sanitizing. They did not sanitize facility properly. Still left ... See Moreempty cups, soda cans, and trash was full at the employees desk whom tested positive for Covid See Less
Reported By SafelyHQ.com User

No Mask Being Worn, Power Ranch Barn pool, Gilbert, AZ, USA

Power Ranch Barn pool, Gilbert, AZ, USA

August 3, 2020 6:53 PM

“Kona Ice shaved ice food truck was at this site and the man serving the shaved ice from the truck wasn’t wearing a mask. See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Olive Garden Italian Restaurant, 24256 El Toro Road, Laguna Woods, California 92637, USA

Olive Garden Italian Restaurant, 24256 El Toro Road, Laguna Woods, California 92637, USA

August 3, 2020 12:00 PM

“T8 CCR ? 3203(a)(4)(C) ? Employees tested positive for Covid-19, and Employer not addressing the hazard effectively.

Source: Osha.gov | Receipt Date: 2020-06-30 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Tropical Smoothie Cafe, 2505 Alpine Ave NW, Grand Rapids, MI 49544, USA

Tropical Smoothie Cafe, 2505 Alpine Ave NW, Grand Rapids, MI 49544, USA

August 3, 2020 12:00 PM

“1. Two employees have been in close contact with COVID-19 positive individuals. One has requested to not work until tested. This request was denied by management and the employee has since come in contact with almost every employee. The employee received a test but still has to work until results ... See Morecome in. It is believed every employee has potentially been exposed as well as customers.



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

Covid-19 OSHA Complaint, BJ's Restaurant & Brewhouse, 4020 Stelzer Rd, Columbus, OH 43219, USA

BJ's Restaurant & Brewhouse, 4020 Stelzer Rd, Columbus, OH 43219, USA

August 3, 2020 12:00 PM

“The employer has not enforced the use of proper personal protective equipment (PPE) and social distancing for employees as a protective measure against the spread of COVID-19.

Source: Osha.gov | Receipt Date: 2020-07-13 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walgreens, Trujillo Alto, 00976, Puerto Rico

Walgreens, Trujillo Alto, 00976, Puerto Rico

August 3, 2020 12:00 PM

“1. Employees with symptoms continue to report to work.
2. Confirmed Employees


Location: Walgreens Plaza Trujillo Alto

Source: Osha.gov | Receipt Date: 20-06-25 See Less
Reported By SafelyHQ.com User

August 3, 2020 12:00 PM

“An employee at the Lawrenceburg Sonic tested positive for COVID-19 on Friday July 31.

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

August 3, 2020 12:00 PM

“An employee of the Sobeys at 700 Terry Fox Dr. in Kanata had tested positive for Covid-19 on July 30 and last worked in the store July 22.

Source: ottawa.ctvnews.ca See Less
Reported By SafelyHQ.com User

August 3, 2020 12:00 PM

“An employee at The Hotel Donaldson and HoDo To Go in Fargo tested positive for COVID-19 on Saturday Aug 1.

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

Recent Interesting Reports

May 26, 2020 9:32 AM

“They're trying to kill me serving me raw chicken See Less
Reported By SafelyHQ.com User

May 20, 2020 11:00 PM

“Company name: Kent Nutrition Group
Brand name: Kent
Product recalled: Home Fresh Starter AMP Crumble
Reason of the recall: Elevated Salt Levels
FDA Recall date: May 20, 2020
Recall details: Company Announcement Kent Nutrition Group (KNG) of Muscatine, Iowa is voluntarily recalling 27- 25 lb.bag ... See Mores of Home Fresh Starter AMP Crumble from a single batch due to elevated salt levels, which can present illness or death to poultry. Kent Nutrition Group has ceased distribution of this lot as FDA and the company continue their investigation. Potential health risks of elevated salt levels include decreased growth rate, increased thirst, weakness, difficulty walking, difficulty breathing and death. To date, KNG has received three complaints concerning this product, which included illnesses and deaths in broilers age 12-20 weeks. This lot was manufactured at the KNG Columbus, NE plant and includes product distributed to select DO IT® Best Hardware Stores in Oregon, Washington, California, Montana and Idaho. Product subject to the recall can be identified by product code 3487 and is identified by the lot code 1020031 stamped onto the white strip sewn used to seal the package. The company is working closely with the Food and Drug Administration (FDA) to further investigate this issue and ensure the recalled products are removed from store shelves and are no longer distributed. Customers who want Information on what to do with the product and or for more information can call Kent Nutrition Group Customer Service at 1-866-647-1212 Monday through Friday from 8 AM to 5 PM Central Time. Customers who have purchased Home Fresh Starter AMP Crumbles lot #1020031 are urged to dispose of or return it to the place of purchase for a full refund.
Check the full recall details on fda.gov
Source: FDA
See Less
Reported By SafelyHQ.com User

July 21, 2020 11:53 AM

“this is RAW CHICKEN. I opened this up and took a bite without realizing it was raw till I smelt it. 🤮🤢 I am so disappointed ☹️ See Less
Reported By SafelyHQ.com User

Food product out dated, Burger King, South Vermont Avenue, Los Angeles, CA, USA

Burger King, South Vermont Avenue, Los Angeles, CA, USA

July 17, 2020 2:21 PM

“totally out dated food product. smell like dead meat
whopper See Less
Reported By SafelyHQ.com User

June 5, 2020 9:34 AM

“They ignoring customers and giving us raw chicken. See Less
Reported By SafelyHQ.com User

May 20, 2020 10:00 PM

“Company name: Biota Biosciences, LLC
Brand name: Biota Biosciences
Product recalled: Cannabidiol (CBD) Complex, Curcumin Complex, Cannabidiol + Curcumin
Reason of the recall: Unapproved new drug
FDA Recall date: May 20, 2020
Recall details: Biota Biosciences is voluntarily recalling the followi ... See Moreng lots in the table below of Cannabidiol (CBD) Complex, Curcumin Complex, and Cannabidiol + Curcumin Injectables to the customer level. These injectable products are being recalled because they were marketed without FDA approval. The products claims on our website make these products unapproved new drugs. Further, the products are misbranded because the labeling fails to bear adequate directions for use.

- Product Name: Cannabidiol(CBD)Complex / Strength(mg): 40 / Multiple Dose Vial Size: 10 mL / Lot: 2H071219P / Expiration: 07/12/2021

- Product Name: Cannabidiol(CBD)Complex / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 10102019P / Expiration: 10/10/2021

- Product Name: Curcumin Complex / Strength(mg): 40 / Multiple Dose Vial Size: 10 mL / Lot: 2H071219CCD / Expiration: 07/12/2021

- Product Name: Curcumin Complex / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 0712019CCD / Expiration: 07/12/2021

- Product Name: Cannabidiol + Curcumin / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 10102019PC / Expiration: 10/10/2021

Risk Statement: Unapproved new drugs injected into the bloodstream for which safety and efficacy have not been established could pose a serious risk of harm to users because they bypass many of the body’s natural defenses against toxic ingredients, toxins, or dangerous organisms that can lead to serious and life-threatening conditions such as septicemia or sepsis. Biota Biosciences has not received any reports of adverse events related to this recall.

Risk Statement: Unapproved new drugs injected into the bloodstream for which safety and efficacy have not been established could pose a serious risk of harm to users because they bypass many of the body’s natural defenses against toxic ingredients, toxins, or dangerous organisms that can lead to serious and life-threatening conditions such as septicemia or sepsis. Biota Biosciences has not received any reports of adverse events related to this recall.

Cannabidiol (CBD) Complex was marketed to suppress pain and aid in the detoxification processes as a promising therapeutic for a wide array of disorders such as epilepsy, including many challenging neuropathy conditions. Curcumin Complex was marketed as a potent anti-inflammatory and antioxidant that may also help improve symptoms of depression and arthritis. Cannabidiol + Curcumin was marketed as a more efficient therapeutic effect. The product was sold to certified practitioners who further administer to customers. The product is packaged in 10 mL sterile vials. Products were distributed Nationwide in the USA and one consignee in New Zealand.

Water Soluble 40mg/10m products can be identified by the labels attached.

Water Soluble 500mg/10m products can be identified by the labels attached.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

Roach, Latin Cafe 2000 - Brickell, Brickell Plaza, Miami, FL, USA

Symptoms: Other
Latin Cafe 2000 - Brickell, Brickell Plaza, Miami, FL, USA

March 14, 2020 4:21 PM

“Roach in my soup. A ROACH. See Less
Reported By SafelyHQ.com User

June 11, 2020 1:00 PM

“Company name: Lupin Pharmaceuticals, Inc
Brand name: Lupin
Product recalled: Metformin Hydrochloride Extended-release Tablets
Reason of the recall: Detection of N-Nitrosodimethylamine (NDMA)
FDA Recall date: June 11, 2020
Recall details: Lupin Pharmaceuticals Inc. is voluntarily recalling Met ... See Moreformin Hydrochloride Extended-Release Tablets USP (generic equivalent of Fortamet®), 500mg, lot G901203 to the consumer level. FDA analysis revealed that this lot exceeded the Acceptable Daily Intake Limit for the impurity N-Nitrosodimethylamine (NDMA). To date, Lupin Pharmaceuticals Inc. has not received any reports of adverse events related to 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, 500mg is a prescription oral medication indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus. It is packaged in a bottle containing 60 tablets with NDC 68180-336-07. The affected lot of Metformin Hydrochloride Extended-Release Tablets USP, 500mg is included in below table:

- Product Name: Metformin Hydrochloride Extended-Release Tablets USP, 500mg

- NDC: 68180-336-07

- Lot Number: G901203

- Expiration Date: 12/2020

The product can be identified by the NDC and the lot number available on the side of the bottle label. Metformin Hydrochloride Extended-Release Tablets USP, 500mg was distributed nationwide in the USA to wholesalers, distributors, and mail order pharmacies.

Lupin Pharmaceuticals Inc. is notifying its wholesalers, distributors, and mail order pharmacies by phone and through recall notification and is arranging for the return of all the recalled product lot. Patients taking Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, are advised to continue taking their medication and contact their pharmacist, physician, or medical provider for advice regarding an alternative treatment. According to the U.S. Food & Drug Administration, it could be dangerous for patients with this serious condition to stop taking their metformin without first talking to their health care professionals.

Check the full recall details on fda.gov

Source: FDA
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

Droppings of a rat or mouse, Chipotle Mexican Grill, 53rd St, Chicago, IL 60615, United States

Chipotle Mexican Grill, 53rd St, Chicago, IL 60615, United States

July 27, 2020 12:17 AM

“I ordered a bowl and I seen like the Droppings of a rat or mouse in there plus maybe the anus cut up with some still stuck in there . See Less
Reported By SafelyHQ.com User