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Dublin, California, United States

Updated: January 14, 2021 12:00 PM

Covid-19 OSHA Complaint, Dublin Nissan, 6450 Dublin Court, DUBLIN, CA, 94568, USA

Dublin Nissan, 6450 Dublin Court, DUBLIN, CA, 94568, USA

January 14, 2021 12:00 PM

“The employer failed to provide deep cleaning after six employees within the facility have tested positive. The employer shall clean and disinfect areas, material, and equipment used by a COVID-19 case during the high-risk exposure period. T8 CCR 3205(c)(8)(C)(3)

Alleged Hazards: 1, Employees Expos... See Moreed: 1
Source: Osha.gov | Receipt Date: 2020-12-11
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Dublin Nissan, 6450 Dublin Court, DUBLIN, CA, 94568, USA

Dublin Nissan, 6450 Dublin Court, DUBLIN, CA, 94568, USA

January 14, 2021 12:00 PM

“1. T8 CCR 3203(a)(4) & (6) The employer is not following COVID-19 protocols by notifying employees who work in close quarters with employees who have tested positive for COVID-19. Employees have been found to test positive in two different departments in the last two weeks, and the employer has not... See Moreinformed employees within those departments.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-23
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Chipotle, 5240 Dublin Blvd., DUBLIN, CA, 94568, USA

Chipotle, 5240 Dublin Blvd., DUBLIN, CA, 94568, USA

December 30, 2020 12:00 PM

“T8 CCR 3205(c)(1)(D) The employer failed to communicate information about COVID-19 hazards to employees within the workplace in accordance with Section (c)(3)(B)(3) of this standard after an employee within the facility tested positive for COVID-19 while in the workplace.

Alleged Hazards: 1, Emplo... See Moreyees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-12-07
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Dublin Honda, 6300 Dublin Blvd., DUBLIN, CA, 94568, USA

Dublin Honda, 6300 Dublin Blvd., DUBLIN, CA, 94568, USA

December 30, 2020 12:00 PM

“1. The employer failed to provide gloves for employees who are required to clean the restrooms using COVID-19 disinfecting products. T8 CCR 3203(a)(4) & (6) and 3380(d) 2. The employer failed to prevent the entrance or harborage of rodents or other vermin inside of the restrooms, lunch rooms, and sh... See Moreop. T8 CCR 3362(f) 3. The employer failed to ensure that supervisors effectively enforce that employees comply with the requirements to wear a face covering while within 6 feet of distance of other employees at work in order to prevent the spread of SARS-CoV-2, the virus that causes COVID-19. Employees get out of the vehicles and forget to put their face coverings on when within 6 feet of other employees while in the garage. T8 CCR 3203(a)(2), (4) & (6)

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-24
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, LaserAway, 5264 Dublin Blvd., DUBLIN, CA, 94568, USA

LaserAway, 5264 Dublin Blvd., DUBLIN, CA, 94568, USA

December 30, 2020 12:00 PM

“T8 CCR Section 3203(a)(4)(6) The employer did not identify, evaluate, and control hazards from COVID-19 by following internal procedures and screening clients for signs and symptoms of COVID-19 prior to performing services requiring close contact, such as laser hair removal.

Alleged Hazards: 1, Em... See Moreployees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-08-20
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, ParkWood Apartments, 7300 Parkwood Circle, Dublin, CA 94568, USA

ParkWood Apartments, 7300 Parkwood Circle, Dublin, CA 94568, USA

November 18, 2020 12:00 PM

“1. The employer is not identifying workplace hazards and correcting them in a timely manner in reference to COVID-19 safety. Maintenance employees are walking in the rental office, throughout the grounds and into living quarters without wearing masks. T8 CCR 3203(a)(4) & (6) 2. The employer is not i... See Moredentifying workplace hazards and correcting them in a timely manner in reference to COVID-19 safety. Employees have either tested positive for COVID-19 or have worked directly with someone who has tested positive and been sent home for quarantine. Maintenance employees continue to work while showing symptoms of COVID-19 and exposing office personnel. T8 CCR 3203(a)(4) & (6)

Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-20
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Reported By SafelyHQ.com User

April 23, 2020 12:00 PM

“An employee of a Whole Foods store in Dublin has tested positive for COVID-19. The employee hadn’t worked since April 1.

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

Recent Interesting Reports

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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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Reported By SafelyHQ.com User

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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Reported By SafelyHQ.com User

January 4, 2021 11:00 AM

“Company name: Essaar Inc.
Brand name: Soho Fresh
Product recalled: 70% Rubbing Alcohol
Reason of the recall: Contaminated with Methanol
FDA Recall date: January 04, 2021
Recall details: Company Announcement Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol... See Morein 33.81 oz. clear plastic bottles to the consumer level. FDA analysis of the product revealed it is contaminated with methanol. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, Essar Inc. has not received any reports of adverse events related to this recall. The product is used as an external purpose use rubbing alcohol and is packaged in 33.81 oz. clear plastic bottles with lot number 200528303 and UPC 7502268987367.

Soho Fresh was distributed nationwide to retail stores. Essaar Inc. is notifying its distributors and customers by email and mail and is arranging for the return of all recalled product to Essaar Inc. Consumers that have product which is being recalled should stop using and discard or return to place of purchase or to Essaar Inc. contacting via email or phone or mailing address mentioned above for arrangements of return. Consumers who have purchased this product should not open the package or use the contents. Instead, they should return the product to the location of purchase for a full refund or call Essaar Inc. at 201-647-7606 Monday to Friday 9am to 5pm, Eastern Standard Time. Essaar Inc. can also be reached via email at essaarinc@yahoo.com.

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

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

January 16, 2021 3:36 PM

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January 1, 2021 8:08 AM

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December 29, 2020 1:59 PM

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