Product: Food Court

Updated:

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Mon Power has scheduled a planned power outage that will affect a portion of the WVU Morgantown Campus from 9 a.m. to noon Wednesday, June 7. Crews will be using this time to upgrade existing equipment. The following campus buildings will be affected: Arnold House, Bicentennial House, … See More
Environmental Health and Safety, Morgan House, Motor Pool, Mountainlair Food Court, The Center for Black Culture, and The Daily Athenaeum.

In case of inclement weather, the outage will be rescheduled from 9 a.m. to noon Thursday, June 8.

Outage link: outages.firstenergycorp.com/mdwv.html
Source: enews.wvu.edu/articles/2023/05/31/power-outage-will-affect-a-portion-of-campus-next-week
Published: 2023-05-31
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#firstenergy #poweroutage #pattesondrive #morgantown #westvirginia #us

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No face masks worn by staff. Litter throughout facility to include trash on floors, dirty bathrooms. No cleaning or sanitizing of spectator areas or food court area. No capacity restrictions, masks of spectators not enforced. The facility is filthy and masks not worn.


Source: Osha.gov | Receipt … See More
Date: 2020-11-16
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#foodcourt #coronaviruscovid19 #osha #11825technologydrive #fishers #indiana #us #foodcourt

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1. The employer has absence policies that are punitive. Employees have come into work when they are experiencing symptoms of COVID-19 because of the employer's absence policies. The employer does not enforce the use of face masks among employees who have come into work while experiencing symptoms … See More
of COVID-19 potentially exposing co-workers to SARS-CoV-2. Employees are within six feet of each other in the food court and at security podiums. 2. During the prior week, the employer has had employees in the food court come into work after testing positive for COVID-19. The employer does not enforce the use of face masks among employees potentially exposing co-workers to SARS-CoV-2. Employees are within six feet of each other in the food court.


Source: Osha.gov | Receipt Date: 2021-12-20
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#foodcourt #coronaviruscovid19 #osha #210racetrackroad #washington #pennsylvania #us #foodcourt

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The employer is not enforcing the Governor's Directive regarding: 1. In the casino, the property is not taking any steps to ensure public compliance with the face covering requirements of emergency directive 024. 2. In the food court area franchise food establishments are not taking steps to … See More
ensure public compliance with face covering requirements. 3. The casino has not implemented social distancing practices in the gaming areas. Patrons are exposing employees to infection hazard. Hazard Location: Casino/Hotel 06/30/2020 EM

Alleged Hazards: 3,
Source: Osha.gov | Receipt Date: 2020-06-30
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#coronaviruscovid19 #osha #4949northranchodrive #lasvegas #nevada #us #foodcourt

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employees not wearing mask or social distancing when meeting are being help in the food court and not enforcing the social distancing rule. left several messages w/no response, sent letter via certified mail 1/6/2021


Source: Osha.gov | Receipt Date: 2021-01-06

#coronaviruscovid19 #osha #3500southmeridian #puyallup #washington #us #foodcourt

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T8 CCR 3205(a)(6) Customers eating inside and outside at Food Court and also walking around the mall without face coverings and they are possibly infecting employees working in the mall with COVID-19.

Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-01-11

#coronaviruscovid19 #osha #2774livermoreoutletsdrive #livermore #california #us #foodcourt

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The employer is not enforcing the use of face masks by employees working at the food court, exposing them to health hazards. T8 CCR 3203(a)(4) & (6)

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-07

#coronaviruscovid19 #osha #2996telegraphavenue #berkeley #california #us #foodcourt

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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

#coronaviruscovid19 #harrahshotelscasino #osha #3475southlasvegasboulevard #lasvegas #nevada #us #foodcourt

Recent Interesting Reports

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An package from Heather s Motty, Union City, NJ, USA

3 weeks ago •reported by user-tjkd2133

I received a package from Heather s Motty Union City NJ today I have no idea what it is & no memory of ordering anything from them.

#unorderedpackage #delivery #unioncity #newjersey #us

D

user-dqfx6869

I ordered and received a product but when plugged into HDMI nothing happened, I would like to get my
Money back

C

user-cvgc6761

Got the same thing ,you plug it into HDMI?

In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium … See More
Chloride Irrigation USP and Sterile Water for Irrigation USP. The Nurse Assist recall was issued due to the potential for a lack of sterility, which could result in non-sterile products. Medline Industries, LP has received one adverse event associated with product manufactured by Nurse Assist.

Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.

The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.

Consumers who have recalled product should stop using the product and contact Medline immediately.

Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.

In case you experience 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. If symptoms persist, seek medical care.

Company name: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-convenience-kits-containing-nurse-assist-09-sodium
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#medicaldevices #recall #us

Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good … See More
manufacturing practice (cGMP) requirements. To date, Honeywell Safety Products USA, Inc. has not received any reports of adverse events related to this recall.

The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.

- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.

- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651

Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.

Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.

Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
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#recall #drugs #us

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