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Harrah's Hotels & Casino

Updated: March 17, 2021 12:00 PM
1. Guest room attendants have been told they now have to clean-up stayover rooms and employees are concerned about potential exposure to COVID-19.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-04 See Less
216


1. Social distancing is not being maintained by persons/patrons within the establishment around the bars, table games, and slot machines. 2. The employer is operating at more than 25% capacity and making it hard for employees to socially distance from the patrons. 3. The employer is not... See More monitoring and managing capacity within the establishment.

Alleged Hazards: 3,
Source: Osha.gov | Receipt Date: 2020-12-27
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216


Security Public Safety Office in the performance of assigned duties: 1. Employees were potentially exposed to Covid-19 due to a coworker who had testing positive for the virus. 2. Employees were not informed of the potential exposure 3. Social distancing had not been followed around card tables... See More and gaming machines. Employees were potentially exposed to covid-19

Alleged Hazards: 3, Employees Exposed: 500
Source: Osha.gov | Receipt Date: 2020-11-17
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2.3K


1) Security not allowed to enforce mask mandate, puts employees at risk of covid-19.

Alleged Hazards: 1, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2020-09-02 See Less
1.0K


1. People have tested positive for COVID-19 but they have not closed the department. Employees fear an exposure to COVID-19.

Hazard Location:
Food court and bars.

8/12/2020
bb

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-08-05 See Less
2.0K


1. Hot water is not available for employees to wash their hands with that work in McLennan's Sports Bar. There has been no hot water for the last two months.
2. Bartenders working in McLennan's Sports Bar are standing/working in approximately 1 inch of water on a... See More daily basis.
3. Mold is growing on the orange painted wall inside McLennan's Sports Bar. Every so often, the employer paints over the mold, but does not remove it. Employees are developing respiratory issues due to working around the mold.
4. Plug in fans are used in McLennan's Sports Bar due to poor ventilation. In turn, the fans are displacing and blowing the mold into the air resulting in employees developing respiratory issues.
5. Draught beer dispensers are not working properly resulting in the harborage of fruit flies and other insects.
6. The employer has not established work practices to ensure employees can effectively socially distance when working in public spaces to help prevent the spread of COVID-19.

Alleged Hazards: 6,
Source: Osha.gov | Receipt Date: 2020-09-10
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216


1. The employer is requiring employees to wear a surgical mask and a face shield when dealing cards on the casino floor. This has caused one employee to struggle at breathing and have dizzy spells.

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-07-06 See Less
216


CDC recommendations were not being followed:
1. Employees were being allowed to work while sick and/or not passing temperature checks.
2. Employees and customers not wearing face coverings while indoor the facility and exterior entertainment/lounge and pool areas.
3. Social Distancing was not being practiced.
4. No... See More plexiglass partitions and/or adequate barriers were not set up for cashiers and customer service areas.
5. Inadequate cleaning of machines, common areas, and bathrooms.
6. Not enough sanitation stations were not set up for employee use.
7. 25 or more casino employees had contracted COVID -19 since opening in May 2020.
8. 2 employees were hospitalized for contracting COVID -19 from working at the casino.

Alleged Hazards: 1, Employees Exposed: 3000
Source: Osha.gov | Receipt Date: 2020-07-23
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2.3K


1. The employer is not effectively adopting and enforcing measures promulgated by the Nevada State Occupational Safety and Health Administration (NV OSHA) to minimize the risk of spread of COVID-19, including social distancing and sanitation measures.

2. The employer is not ensuring that all patrons, customers, or... See More clients utilize face coverings to minimize the risk of spread of COVID-19.


Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-02
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216


1. Employees at the property have been exposed to covid-19.
2. One employee was taken aware in an ambulance with a high fever and breathing issues, and subsequently tested positive.
3. Other employees worked in close proximity to that employee, but still have to report to work.... See More Hazard Location:
Within the workplace.

7/14/2020
JH

Alleged Hazards: 3,
Source: Osha.gov | Receipt Date: 2020-07-06
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2.0K


Recent Interesting Reports

Nottingham, NH, Buzzagogo Inc. is voluntarily recalling one lot of Allergy Bee Gone for Kids Nasal Swab Remedy to the consumer level due to potential microbial contamination. FDA testing found some product to contain elevated levels of yeast & mold and may contain the bacteria Bacillus cereus.... See More Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, was distributed Nationwide to wholesale distributors, retail stores and online on Amazon.com and the company web site. Buzzagogo, Inc. places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process.

Risk Statement: In immunocompromised patients, the use of the affected product could potentially result in severe or life-threatening adverse events such as bacteremia/sepsis, pneumonia, invasive fungal rhinosinusitis, or disseminated fungal infection. In non-immunocompromised patients, the population most likely to use the product, the use of the defective product may result in infectious complications, for instance bacteremia or noninvasive fungal rhinosinusitis, but in this population the infections are expected to be less severe and more readily responsive to treatment. To date, Buzzagogo, Inc. has not received any complaints related to microbial concerns or reports of adverse events related to this recalled lot.

The product is used to lessen seasonal allergy symptoms and is packaged in individual tubes for topical nasal application. The affected Allergy Bee Gone for Kids Nasal Swab Remedy lot is 2006491 with expiration date 8/2024 and UPC code 860002022116. The product can be identified by locating the lot number and expiration date on the bottom of the product carton.

Buzzagogo, Inc. is notifying its distributors and customers by email and is arranging for return or replacement of all recalled products. Consumers, distributors or retailers that have Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, should stop using the product, and discard any remaining product.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.

Company name: Buzzagogo Inc.
Brand name: Allergy Bee Gone for Kids
Product recalled: Nasal Swab Remedy
Reason of the recall: Product contains elevated levels of Bacillus cereus
FDA Recall date: June 07, 2022

Source: fda.gov
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440


Latin Foods Market is voluntarily recalling one lot, LOTE 334 21, of Artri King Reforzado con Ortiga y Omega 3 tablets to the consumer level. FDA analysis has found the product to be tainted with diclofenac and dexamethasone. The product was distributed Nationwide in the USA, it... See More was sold online at www.latinfoods.com, and in retail stores. To date, Latin Foods Market has not received any reports of adverse events related to this recall.

Diclofenac and dexamethasone are both FDA approved drugs. Diclofenac is a non-steroidal anti-inflammatory drug (NSAID) indicated for the management of pain and arthritis and dexamethasone is a corticosteroid indicated for a variety of indications including but not limited to arthritis. The presence of diclofenac and dexamethasone in Artri King Reforzado con Ortiga y Omega 3 renders it an unapproved drug for which the safety and efficacy has not been established and, therefore, subject to recall.

Risk Statement: Consumption of undeclared diclofenac could result in serious adverse events that include cardiovascular, gastrointestinal, renal, and anaphylaxis in patients taking concomitant NSAIDs and/or anticoagulants, in those who have allergies to diclofenac, or those with underlying illnesses. Consumption of undeclared dexamethasone may lead to severe and serious adverse events such as adrenal suppression, a disorder in which the adrenal glands do not produce enough hormones, and adverse consequences can range from limited adverse consequences to death.

Artri King Reforzado con Ortiga y Omega 3 is marketed as a dietary supplement for relief of pain and inflammation associated with arthritis and osteoarthritis and is packaged in 100-count tablets per bottle within a cardboard carton, UPC 7 501031 111138. Latin Foods Market will notify all customers who ordered the product online in writing with an email instructing them to discard all recalled products after reviewing the FDA public notification link below and will post a copy of this press release on the Latin Foods Market website and in the retail stores where it was sold.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.  

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Latin Foods Market
Brand name: Arti King
Product recalled: Artri King Reforzado con Ortiga y Omega 3
Reason of the recall: Undeclared Diclofenac and Dexamethasone
FDA Recall date: June 14, 2022

Source: fda.gov
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440


6/6/2022, at 2323:43 to be more precise. A significant and extensive sonic boom tore through our house, woke us, terrified our dogs and causes creaking that continued for several more seconds. It is not the “sound of freedom.” It is poor and unaware flying. It is also... See More profoundly disturbing especially in these crazy times. Our dogs didn’t settle for an hour. I didn’t settle until almost 3 am. This can’t be allowed by city ordinance. Extremely disruptive. I do have it on our doorbell and on inside house camera. It was so loud, it tripped the recordings. See Less
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We have been without power since Monday night, this is so uncomfortable having no power along with this high heat and humidity. Even had to throw out the food in the refrigerator. We don’t even have water because of a pump that takes electricity. Thank you See Less
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Received a small pkg envelope with nothing in it Sunbury, Pa. 17801 FIRST-CLASS PKG SVC June 21 2022 Mailed from zip 90021 3oz First Class pkg Size Zone 8 See Less
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Bryant Ranch Prepack Inc. is voluntarily recalling one lot of Morphine Sulfate 30 mg Extended-Release tablets (Comprised of 10 bottles), and one lot of Morphine Sulfate 60 mg Extended-Release tablets (Comprised of 10 bottles) to the consumer level listed below. The products have been found to have... See More incorrect labeling where bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.

Risk Statement: Patients prescribed the 30 mg dose who receive the 60 mg dose could be at risk for overdose and death. Patients prescribed the 60 mg dose who receive the 30 mg dose may experience withdrawal and untreated pain if the dose given is too low. To date, Bryant Ranch Prepack Inc. has not received any reports of adverse events related to this recall.

-Affected products:
Product: Morphine Sulfate Extended-Release Tablets
Strength: 30 mg
Quantity per bottle: 100
NDC: 63629-1088-01
Lot: 179642
Expiration: 11/30/2023

Product: Morphine Sulfate Extended-Release Tablets
Strength: 60 mg
Quantity per bottle: 100
NDC: 63629-1089-01
Lot: 179643
Expiration: 08/31/2023

Morphine Sulfate Extended-Release tablets are used to manage severe pain. The 30 mg tablets are round, purple-colored, film-coated tablets debossed with "RD" and "71" on one side and plain on the other side. The 60 mg tablets are round, light orange-colored, film-coated tablets debossed with "RD" and "72" on one side and plain on the other side.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Bryant Ranch Prepack Inc.
Brand name: Bryant Ranch Prepack Inc.
Product recalled: Morphine Sulfate 30 mg Extended-Release tablets
Reason of the recall: Incorrect labeling
FDA Recall date: June 29, 2022

Source: fda.gov
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440


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