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Mesa, Arizona, United States
Updated: December 23, 2020 4:31 PM
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. ”
The UPS Store, South Power Road, Mesa, AZ, USA
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. ”
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... loyee testing positive for COVID-19.
Alleged Hazards: 3, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-08-14 ”
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... k 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 ”
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 ”
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... 20-07-31 ”
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... Date: 2020-07-17 ”
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... prevent 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 ”
Dutch Bros Coffee, 1326 South Alma School Road, Mesa, AZ, USA
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 ”
Fry's Marketplace, East Main Street, Mesa, AZ, USA
June 29, 2020 9:57 AM
“One employee tested positive for COVID 19 ”
Recent Interesting Reports
Long Island City, Queens, NY, USA
January 14, 2021 8:51 PM
“I am a teacher and am authorized to get the Moderna vaccine. I made an appointment in Ridgewood 2 days ago. Appoint was at 5:20 but didn't get my shot until 7:40. The lines are extremely long at night. But the nurse said they are empty in the morning. Once you get inside it is very fast, everyone is... very helpful and you can sign up for your second vaccine. They make you wait 15 mins to make sure you're ok before you leave. I have no side effects from the shot and feel fine. ”
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... ing (“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.
On February 3, 2020, Luckin issued a press release denying Muddy Waters’s allegations. The Company “categorically denie[d] all allegations in the [Muddy Waters] Report” and assured investors that the “methodology of the Report is flawed, the evidence is unsubstantiated, and the allegations are unsupported speculations and malicious interpretations of events.”
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%.
Luckin Coffee ADSs have now been delisted from trading on the NASDAQ. ”
Pittsburgh, PA, USA
January 19, 2021 10:19 PM
“My puppy Angus, at age 5 months, ate a small amount of a dream bone on Jan 9, 2020 in the afternoon, and then started crying and pacing, not eating any more. About 5 pm, he refused to eat, and went to lie down in his bed, not begging at our table while we ate. He seemed stiff, and lay down with his... neck stretched out. Soon he was unresponsive and glassy-eyed, and stiff as a board. I took him to the Emergency vet, who did not think that there was any obstruction, and while at the vet's he improved, so I brought him home for observation. The vet said that it could be the onset of a neurological condition, or something in the Dreambone. He recovered, is now 18 months (it is more than a year later) and has never had a similar episode. By a process of elimination, it is probable that the Dreambone caused this reaction, and that it wasn't lethal because he only ate a small amount. ”
Blackcass pruner. Only received chain as did many others, apparently. Very deceptive advertising., Edgewater, FL, USA
Edgewater, FL, USA
January 1, 2021 8:08 AM
“Ordered Stihl pruner from Blackcass. 2020 Hot Selling GTA 26 Battery Powered Wood Cutter $29.99. Says style Outdoor Portable Carbon Steel Chain. I assumed this meant the chain was carbon steel. Ad goes on to list what's included. You can view their ads online. Received the chain only. When I contac... ted company, they informed me I had only ordered the chain. Who buys just the chain? I am finding others who are experiencing the same issue. Disputing through PayPal also. Feel this is quite the scam. ”
Langlois, OR, USA
January 16, 2021 3:36 PM
“I ordered a Stihl wood cutter and got an IWORKS mini chain saw that does not work. ”
Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz - recalled due to Potential contamination with Burkholderia lata, USA
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... nc. (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 email@example.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 ”
January 23, 2021 4:13 PM
“Investors who have suffered losses on Luckin Coffee investments have potential legal claims under U.S. securities laws. Investors who purchased Luckin Coffee ADSs may be able to sue Luckin Coffee, the directors of Luckin Coffee, the Company’s auditor and the underwriters of Luckin Coffee to recover... their losses.
Investors who have suffered losses on their purchases of Luckin Coffee ADSs may have strong legal claims under the U.S. securities laws because, Luckin Coffee has now admitted that its 2019 sales were fabricated by senior officers of the Company;
Apart from Luckin Coffee itself, other persons may be potentially liable, including underwriters of Luckin Coffee’s IPO and SO, and Luckin Coffee’s auditors. ”
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. ”
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... roducts 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 firstname.lastname@example.org 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 ”
Los Angeles, CA, USA
January 21, 2021 7:07 PM
“I saw an ad for a blackcass hand held chainsaw. What arrived was only a chain. Never received anything else ”