Flamingo Hotel & Casino, 3555 Las Vegas Blvd South, LAS VEGAS, NV, 89109, USA
Latest report:
Covid-19 OSHA Complaint
2 years ago
1. Employees and customers are coming into the hotel and are sick with COVID-19. The employer is not sending employees home even if they are displaying COVID-19 symptoms.
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2022-01-04
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2022-01-04
1.4K
Covid-19 OSHA Complaint
2 years ago
1.In the North Plant, 1 of 3 possible emergency exit doors is locked and employees are concerned about egress in an emergency. HAZARD LOCATION: North Plant 04/05/2021 KR
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-04-05
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-04-05
1.4K
Covid-19 OSHA Complaint
2 years ago
1. The employer is not following proper quarantine requirements for COVID-19. Employees who are showing symptoms are required to get tested right away and are required to come back to work if negative, even when sick. 2. The hallways of the hotel towers have no air conditioning
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and some floors, such as the 22nd floor, have hot air coming out of the vents. Housekeeping employees working in the hallways and locker rooms, where linens and towels are folded, do not have a cool area to rest. 3. The locker rooms within the hotel towers no longer have water jugs in them. They were removed and employees were instructed to bring their own water with them. If they need more water while working, employees are instructed to buy from the vending machines. 4. Housekeeping employees do not have access to ice. Guests frequently form lines at the ice machines and housekeeping does not have time to wait as they have to meet their quota. Hazard Location: Hallways and locker rooms of hotel towers. 6/21/2021 RAO
Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-06-21
Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-06-21
1.4K
Covid-19 OSHA Complaint
3 years ago
1. The employer is not disinfecting surfaces that are used often. Employees are concerned about exposure to the COVID-19 virus. HAZARD LOCATION: Throughout the casino floor. 10/26/2020 KR
Source: Osha.gov | Receipt Date: 2020-10-21
Source: Osha.gov | Receipt Date: 2020-10-21
1.4K
Covid-19 OSHA Complaint
3 years ago
1. The employer is not complying with the Governor's COVID-19 mandate in regard to high touch areas, such as, casino floor gambling machines, are not being properly disinfected in between players due to the casino reducing the number of employees in the EVS department, which reduces the
…
efficiency of being able to disinfect the casino properly to reduce the probability of spreading the COVID-19 virus. HAZARD LOCATION: Throughout 10/22/2020 KR
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-16
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-16
1.4K
Two employees test positive for COVID-19
3 years ago
Two employees at the Flamingo hotel-casino on the Las Vegas Strip have tested positive for COVID-19.
Source: www.cdcgamingreports.com
Source: www.cdcgamingreports.com
1.4K
Recent Interesting Reports
Silver skull with flower ring, Oxnard, CA, USA
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I received a random ring in the mail I did not order silver with a skull and flowers
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I purchased 5 of your large lighter smoking sets and none of them light., York, PA, USA
4 weeks ago •reported by user-wdvb9628
When I opened the first lighter, it flickered and then lit. When I tried to operate the other 4 lighters, none of them worked. Went back to the first lighter, and it.would not re-light. Plus the lighter boxes are very hard to open,,one of the box lids tore at the top. What do you suggest?
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Brushing scam from Jane, 371 Little Falls Road, Cedar Grove, NJ, USA
3 weeks ago •reported by user-vpnxd669
I’ve seen online that this company sends random items to US residents then post fake reviews on the internet using the supposed buyers name.
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AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence, USA
3 weeks ago •source www.fda.gov
Recall notice
Eugia US LLC (f/k/a AuroMedics Pharma LLC) has initiated a voluntary recall of lot number 3MC23011 of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) - 10mL Vial to the consumer level due to a customer product complaint for the presence of white particles floating
…
inside of the vial.
Administration of an injectable product that contains particulate matter may result in local irritation or swelling. If the particulate matter reaches the blood vessels or is injected intravascularly it can travel to various organs and block blood vessels in the heart, lungs or brain which can cause stroke and even lead to death. To date, Eugia US LLC has not received any reports of adverse events related to this recall.
Methocarbamol injection USP 1000 mg/10 mL (100mg/mL), is used as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. It is packaged in 10 mL and packed as 25 (vials) X 04 (Printed E-Flute cartons) X 01 (Shipper) with NDC code as 55150-223-10. Eugia US LLC shipped the entire lot to wholesalers nationwide from Jan 12, 2024, through Jan 16, 2024.
The product can be identified by product name on carton and vial label and with lot number 3MC23011 and Exp. Date: Nov 2026 (NDC 55150-223-10) (See enclosed vial label). The product label is as shown in the image below.
Eugia US LLC (f/k/a AuroMedics Pharma LLC) is notifying its distributors by recall letters and is arranging for the return/replacement of all recalled products. Wholesalers, hospitals, pharmacies, institutions, and doctors with an existing inventory of the recalled product lot should discontinue use, stop distribution and quarantine the product immediately. If you have further distributed the recalled product lot, notify your accounts and/or any additional locations which may have received the recalled product. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.
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.
If you are experiencing any harm after using this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Eugia US LLC
Brand name: Eugia US LLC
Product recalled: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial)
Reason of the recall: Device & Drug Safety – Presence of Particulate Matter
FDA Recall date: March 28, 2024
Source: www.fda.gov
Administration of an injectable product that contains particulate matter may result in local irritation or swelling. If the particulate matter reaches the blood vessels or is injected intravascularly it can travel to various organs and block blood vessels in the heart, lungs or brain which can cause stroke and even lead to death. To date, Eugia US LLC has not received any reports of adverse events related to this recall.
Methocarbamol injection USP 1000 mg/10 mL (100mg/mL), is used as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. It is packaged in 10 mL and packed as 25 (vials) X 04 (Printed E-Flute cartons) X 01 (Shipper) with NDC code as 55150-223-10. Eugia US LLC shipped the entire lot to wholesalers nationwide from Jan 12, 2024, through Jan 16, 2024.
The product can be identified by product name on carton and vial label and with lot number 3MC23011 and Exp. Date: Nov 2026 (NDC 55150-223-10) (See enclosed vial label). The product label is as shown in the image below.
Eugia US LLC (f/k/a AuroMedics Pharma LLC) is notifying its distributors by recall letters and is arranging for the return/replacement of all recalled products. Wholesalers, hospitals, pharmacies, institutions, and doctors with an existing inventory of the recalled product lot should discontinue use, stop distribution and quarantine the product immediately. If you have further distributed the recalled product lot, notify your accounts and/or any additional locations which may have received the recalled product. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.
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.
If you are experiencing any harm after using this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Eugia US LLC
Brand name: Eugia US LLC
Product recalled: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial)
Reason of the recall: Device & Drug Safety – Presence of Particulate Matter
FDA Recall date: March 28, 2024
Source: www.fda.gov
304
I did not order this product, Greenbelt, Maryland, USA
1 week ago •reported by user-hnby3436
I did not order this KETO PURE
278
I received a parcel for 2 bars of soap that I did not order., Rancho Cucamonga, CA, USA
4 weeks ago •reported by user-jxwc6441
I received a package today, March 25, 2024 that I did not order. The package contains 2 bars of orange soap. There's no lable or anything attached. I looked up the address from where it was shipped from in California. It's a warehouse called Cambria that is
…
no longer in operation. The building is up for sale.
233
I keep getting Keto acv Gummies that I didn't order, Homegardner Road, Castalia, OH, USA
1 week ago •reported by user-xthmq334
I keep getting Gummies I didn't order from DP
192-01 Northern Blvd
Flushing Ny. 11358 "STOP "
192-01 Northern Blvd
Flushing Ny. 11358 "STOP "
48
I just received this package also from Tampa Florida... Subgenix, Houston, TX, USA
2 weeks ago •reported by user-fkkg2382
I didn't order this product is it safe?
1.1K
Empty package, Fishing Creek, MD, USA
1 week ago •reported by user-gnxv8262
Received empty package with sender name of Emily hunt 125 Jackson ave Edison NJ 08837
1
Unordered package, Ontario, Canada
3 weeks ago •reported by user-yjcbc883
Trying to return this package
received by Logistic  895 Meyerside Dr MISSISSIGA ONTARIO CANADA. JY243510U16208****
received by Logistic  895 Meyerside Dr MISSISSIGA ONTARIO CANADA. JY243510U16208****
75
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