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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)

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Mesa, Arizona, United States

Updated: December 23, 2020 4:31 PM

No Masks, Marigold Salon, South Greenfield Road, Mesa, AZ, USA

Marigold Salon, South Greenfield Road, Mesa, AZ, USA

December 23, 2020 4:31 PM

“No employees or customers wearing masks. 100% of the people at this salon are maskless. See Less
Reported By SafelyHQ.com User

December 22, 2020 5:43 PM

“Long line of people dropping off packages. Most people in line didn’t have masks on and were not social distancing. Line was so long it was out the door. See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Universal protection, 1001 W Southern Ave, MESA, AZ, 85210, USA

Universal protection, 1001 W Southern Ave, MESA, AZ, 85210, USA

December 9, 2020 12:00 PM

“1. The employer is not providing personal protective equipment (PPE) to employees to prevent the spread of COVID-19 in the workplace. 2. CDC guidelines are not followed when an employee tests positive for COVID-19 to quarantine them. 3. The employer is not disinfecting the workplace following an emp... See Moreloyee testing positive for COVID-19.

Alleged Hazards: 3, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-08-14
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Sossoman Dental health and Implant Center, PC, 1228 Sossoman Rd, MESA, AZ, 85209, USA

Sossoman Dental health and Implant Center, PC, 1228 Sossoman Rd, MESA, AZ, 85209, USA

December 9, 2020 12:00 PM

“1.The employer is not following current CDC guidelines to prevent the spread of COVID-19 in the workplace. 2.The employer is not wiping down commonly touched surfaces throughout the facility. 3.Thermometer used for temperature checking is not wiped down between staff. 4.The Office Manager uses a mas... See Morek sometimes. 5.Employees do not use masks correctly and management does not do anything about it.

Alleged Hazards: 5, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-08-17
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Red Mountain Endodontics, PC, 3048 E Baseline Rd, MESA, AZ, 85204, USA

Red Mountain Endodontics, PC, 3048 E Baseline Rd, MESA, AZ, 85204, USA

December 9, 2020 12:00 PM

“1. The employer is not following current CDC guidelines to prevent the spread of COVID-19 in the workplace. 2. Patients are visiting the lobby without face masks to protect the employees.

Alleged Hazards: 2, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-08-13 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, RTH Enterprises, 1210 E main St, MESA, AZ, 85204, USA

RTH Enterprises, 1210 E main St, MESA, AZ, 85204, USA

December 9, 2020 12:00 PM

“1. The employer is not following current CDC guidelines to prevent the spread of COVID-19 in the workplace. 2. Employees who have signs and symptoms of COVID-19 are not required to isolate or quarantine by the employer.

Alleged Hazards: 1, Employees Exposed: 25
Source: Osha.gov | Receipt Date: 20... See More20-07-31 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Montecito Post Acute Care and Rehabilitation, 51 S. 48th St, MESA, AZ, 85206, USA

Montecito Post Acute Care and Rehabilitation, 51 S. 48th St, MESA, AZ, 85206, USA

December 9, 2020 12:00 PM

“1. The employer is not following current CDC and OSHA guidelines for preventing the spread of the virus in the workplace. 2. Management is asking those tested positive employees to return to work with signs and symptoms present.

Alleged Hazards: 2, Employees Exposed: 20
Source: Osha.gov | Receipt... See MoreDate: 2020-07-17 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Nammo Defense Systems Inc., 4051 Higley Rd, MESA, AZ, 85215, USA

Nammo Defense Systems Inc., 4051 Higley Rd, MESA, AZ, 85215, USA

December 5, 2020 12:00 PM

“1. An employee is not wearing a mask in the workplace to prevent the spread of COVID-19. 2. is aggressive with employees in the workplace to include pushing them, yelling at them and catching them with his elbows. 3. The employer does not provide Personal Protective Equipment (PPE) for employees to... See Moreprevent the spread of COVID-19 in the workplace. 4. The employer does not enforce CDC recommendations for social distancing to prevent the spread of COVID-19 in the workplace. 5. The employer requires employees who have tested positive for COVID-19 to report to work. 6. The employer is covering up employee's exposures to chemical skin and respiratory irritants. 7. There is a lack of PPE for employees exposed to health and safety hazards. 8. The employer requires employees to use products after known safety concerns were raised. 9. An employee, who was pregnant, was exposed to harmful chemicals thus causing birth defects to her child. 10. Employees work more than 8 hours a day and are prone to accidents and fatigue. 11. Heavy materials are stored in an unsafe manner. 12. Employees are encourage to work through injuries without reporting them to supervision or management. 13. The employer requires employees to lift heavy objects using procedures that are unsafe. 14. Employees are exposed to retaliatory actions when safety issues are brought up, when they have been injured or need time off to seek treatment. Forms of retaliation are; changing an employee's assignments to less-desirable duties in other work areas or departments. They discourage and withhold advancement opportunities including denying promotions. Assessing an employee's performance with poor ratings when they are away and recovering from a workplace exposure or injury.

Alleged Hazards: 14, Employees Exposed: 250
Source: Osha.gov | Receipt Date: 2020-07-31
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Reported By SafelyHQ.com User

July 8, 2020 12:00 PM

“A Dutch Bros employee at 1326 S. Alma School Road in Mesa has tested positive for COVID-19. The employee last worked from June 13-17

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

June 29, 2020 9:57 AM

“One employee tested positive for COVID 19 See Less
Reported By SafelyHQ.com User

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January 23, 2021 3:32 PM

“Luckin Coffee is a coffee retailer founded in 2017 based in Xiamen, the People’s Republic of China. Luckin Coffee owns and operates stores selling food and beverages, as well as a mobile application for food and beverage purchases.

On May 17, 2019, Luckin Coffee conducted an Initial Public Offer... See Moreing (“IPO”) of its ADSs.

On January 31, 2020, Muddy Waters Research published a report stating that Luckin Coffee had fabricated portions of its financial statements beginning in the third quarter of 2019, citing “smoking gun evidence” such as thousands of hours of store video, customer receipts, and monitoring of the Company’s mobile application data. On this news, the price of Luckin Coffee ADSs fell from $36.40 per share on January 30, 2020, to $32.49 per share on January 31, 2020.

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On April 2, 2020, contrary to its previous denials, Luckin Coffee disclosed that it had conducted an internal investigation and had found that Luckin Coffee’s Chief Operating Officer Jian Liu and several of his direct reports had fabricated over $300 million of sales beginning in the second quarter of 2019. On this news, the price of Luckin Coffee ADSs fell from $26.20 per share on April 1, 2020 to $6.40 per share on April 2, 2020 – a decline of over 75%.

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December 28, 2020 8:00 PM

“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 28, 2020
Recall details: Schaumburg, Illinois, Sunstar Americas, I... See Morenc. (SAI) is voluntarily recalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 12/31/2020 – 9/30/2022 to the consumer level. This product may be contaminated with the bacteria Burkholderia lata. This is an expansion of the recall initially announced on October 27, 2020. Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia.

To date, 29 adverse events have been reported to SAI related to this recall. Affected patients tested positive for Burkholderia lata infections, typically found in sputum cultures while under treatment for other serious medical conditions. Use of the contaminated product on patients with pre-existing respiratory conditions, including those infected with Covid-19, is particularly unsafe.

The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:

- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.

The product can be identified as shown in the images below Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers follow below:

-Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 16 fl.oz. Amber Bottles. NDC #: 052376-021-02. Product Code: 1789P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022

- Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 4 fl.oz. Amber Bottles NDC #: 052376-021-04. Product Code: 1788P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022.

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. Complete and submit the report Online Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. Sunstar is committed to delivering safe, fully compliant products of the highest quality and is taking necessary steps to prevent future occurrence of this issue. 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
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January 23, 2021 4:13 PM

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Moderna COVID-19 injection, Mount Pleasant, SC, USA

Symptoms: Fatigue
Mount Pleasant, SC, USA

January 22, 2021 12:40 PM

“Adverse reaction in arm now requires surgery. Orthro surgeon, MRI confirm the damage is from reaction not needle placement. Also, extreme fatigue, had tremors and brain fog. See Less
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December 30, 2020 10:00 PM

“Company name: Sportmix
Brand name: Sportmix
Product recalled: Dog and Cat Food
Reason of the recall: Elevated levels of aflatoxin
FDA Recall date: December 30, 2020
Recall details: Midwestern Pet Foods, Inc., of Evansville, IN is issuing a voluntary recall of the below-listed dog and cat food p... See Moreroducts due to tests indicating levels of Aflatoxin that exceed acceptable limits. Products were distributed nationally to online distributors and retail stores. Aflatoxin is a toxin produced by the mold Aspergillus flavus, which can grow on corn and other grains used as ingredients in pet food. At high levels, aflatoxin can cause illness and death in pets.

There have been reports of illnesses and deaths in dogs associated with the below listed lots of Sportmix High Energy. No cat or human illnesses have been reported. If your pet shows signs of aflatoxin poisoning including sluggishness, loss of appetite, vomiting jaundice (yellowish tint to the eyes, gums, or skin due to liver damage), and/or diarrhea, contact a veterinarian immediately. Provide a full diet history to your veterinarian. It may be helpful to take a picture of the pet food label, including the lot number. Lot code information may be found on the back of the bag and will appear in a three-line code, with the top line in the format “EXP 03/03/22/05/L#/B###/HH:MM” as follows (see below in pictures section).

Retailers and distributors should immediately pull recalled lots from their inventory and shelves. Do not sell or donate the recalled products. Retailers are encouraged to contact consumers who have purchased the recalled products if you have the means to do so (frequent buyer cards, etc.).

Pet parents: do not feed the recalled products to your pets or any other animals. Destroy the products in a way that children, pets, and wildlife cannot access them. Wash and sanitize pet food bowls, cups, and storage containers. Contact Midwestern Pet Foods Consumer Affairs at 800-474-4163, ext. 455 from 7AM to 4PM Central Time, Monday through Friday, or by email at info@midwesternpetfoods.com for additional information. This is a voluntary recall conducted in cooperation with the U.S. Food and Drug Administration.

Recalled lot codes are as follows:

- 50# Sportmix Energy Plus Lots Exp 03/02/22/05/L2, 03/02/22/05/L3, 03/03/22/05/L2
- 44# Sportmix Energy Plus Lots 03/02/22/05/L3
- 50# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 44# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 31# Sportmix Original Cat Lots 03/03/22/05/L3
- 15# Sportmix Original Cat Lots 03/03/22/05/L2, 03/03/22/05/L3

Products may be identified as follows (see pictures below).

Check the full recall details on fda.gov

Source: FDA
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