Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Use camera
Select from library
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!
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)
Visit our learn pages for more helpful information or, email us: support@safelyhq.com
Goodbye! and best wishes in your recovery
Report by
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

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)

If your report is poison related call 1-800-222-1222 for a free consultation with a live medical poisoning expert

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Ralphs, 10901 Ventura Blvd, Studio City, CA 91604, USA

Total all time reports:  3
Latest report: November 25, 2020 12:00 PM

Covid-19 OSHA Complaint

November 25, 2020 12:00 PM

“Look Article 10: PPE requirements for General Industry: 3380(a), and 3384(a) Also look for §5199. Aerosol Transmissible Diseases. Complainant states, ¿Store too crowded and not being monitored check stands not being sanitized every half hour . They are letting customers with no mask in to buy grocer... See Moreies and not saying anything to them . We have almost 200 employees so all employees who are scheduled to work are exposed on a daily basis¿

Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-04-26
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint

November 25, 2020 12:00 PM

“Look Article 10: PPE requirements for General Industry: 3380(a), and 3384(a) Also look for §5199. Aerosol Transmissible Diseases. Complainant states, ¿This store is not following CDC guidelines and is allowing as many people in the store at a time until it reaches a critical amount and only then tak... See Morees action. Today Saturday 4/24 at 245 pm the store became way overcrowded and only after several employees and customers complained did they close the door. There is such constant business that check stands are not being sanitized. Employees are not washing there hands every 30 minutes. Only on lunch or break. Signs are up stating carts are sanitized yet they are none be cleaned. Bathrooms are not being cleaned or sanitized every 1/2 hour. The store is the only location where they are not limiting the number of people allowed in the store. They are more interested in reaping in more sales and do not care about the health of the employees.¿ T8 CCR 3203(a)(4)(6)/ Employer is allowing too many people in without masks overcrowding the store and employees are working closer than 6 feet of others in violation of CDC COVID-19 infection control procedures. T8 CCR 3362, 3380(f)/ Check stands are carts are not being sanitized and bathrooms are not being cleaned and sanitized. Employees are not washing their hands.


Source: Osha.gov | Receipt Date: 2020-04-25
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint

October 27, 2020 12:00 PM

“1. The employer is not enforcing customers to wear facial covering.
2. Employees are not protected by plastic barrier at the self-checkout stands. Customers buying alcohol at the self-checkout stand have to take out their mask to verify their age resulting in exposure to employees.
3. Employer h... See Moreas not develop a system and procedures to maintain six feet distances among customers and employees.
4. Employer lets everyone come in the store at the same time.

Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-04-20
See Less
Reported By SafelyHQ.com User

Related Reports

Covid-19 OSHA Complaint, Pacific Rail Services, 98 Cabot Blvd E, Langhorne, PA 19047, United States

Pacific Rail Services, 98 Cabot Blvd E, Langhorne, PA 19047, United States

November 25, 2020 12:00 PM

“1. Employees are asked to use a guard shack that is without an overhang and has a bad roof leak during rain. 2. Employees are asked to use a guard shack that has no heat due to a missing door 3. Four security guards employees are asked to use a guard shack where social distancing cannot be maintaine... See Mored

Alleged Hazards: 3, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2020-10-16
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Tower Oaks by Pulte Homes, 5 Preserve Pkwy, Rockville, MD 20852, United States

Tower Oaks by Pulte Homes, 5 Preserve Pkwy, Rockville, MD 20852, United States

November 25, 2020 12:00 PM

“Possibly employees are exposed to COVID-19 where engineering, administrative, and work practice controls are not implemented to protect employees. Possibly employees are exposed to COVID-19 where personal protective equipment (PPE) was not provided. Possibly employees are exposed to COVID-19 where h... See Moreandwashing facilities and chemicals used for disinfecting were not provided.

Alleged Hazards: 3, Employees Exposed: 200
Source: Osha.gov | Receipt Date: 2020-04-03
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Departamento de Justicia de PR, Av. Jesús T. Piñero, San Juan, 00918, Puerto Rico

Departamento de Justicia de PR, Av. Jesús T. Piñero, San Juan, 00918, Puerto Rico

November 25, 2020 12:00 PM

“1- Employer does not follow the protocols in his exposure control plan, when there are positive cases in the workspace. 2- Lack of training on the exposure control plan.

Alleged Hazards: 2, Employees Exposed: 70
Source: Osha.gov | Receip Date: 2020-09-15 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Hipódromo Camarero, Av. 65 de Infantería, Canóvanas, Puerto Rico

Hipódromo Camarero, Av. 65 de Infantería, Canóvanas, Puerto Rico

November 25, 2020 12:00 PM

“There were cases of positive employees and did not isolate employees exposed to them.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receip Date: 2020-10-23 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Red White & Blue Thrift Store, 935 Ohio River Blvd, Pittsburgh, PA, USA

Red White & Blue Thrift Store, 935 Ohio River Blvd, Pittsburgh, PA, USA

November 25, 2020 12:00 PM

“1. There are missing/broken floor tiles in three areas of the store creating tripping hazards. The locations of the floor tiles are outside of the office, behind the registers and in the main aisle of the backroom. 2. The employer did not follow Pennsylvania Department of Health and Centers for Dise... See Morease Control and Prevention (CDC) guidelines for quarantining employees upon return from high risk areas.

Alleged Hazards: 2, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-08-21
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Stowe Town Electric Department, 435 Moscow Road, Stowe, VT 05672, USA

Stowe Town Electric Department, 435 Moscow Road, Stowe, VT 05672, USA

November 25, 2020 12:00 PM

“Electrical Department Office: Concerns over exposure to COVID-19 due to lack of social distancing and employer not enforcing the wearing of face coverings when employees are unable to maintain 6 feet or more distance between each other. Additional area of concern: Copier and postage machine are loca... See Moreted in an area very close to two worker cubicles such that someone using these machines are likely to be within six feet of one or both of these coworkers. In addition, these same cubicles are situated so they share a common cube wall. The two people working in these cubes are only four feet or so away from each other, and do not always wear masks.


Source: Osha.gov | Receipt Date: 2020-05-18
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Rosetta Radiology, 1421 3rd Avenue, New York, NY 10028, USA

Rosetta Radiology, 1421 3rd Avenue, New York, NY 10028, USA

November 25, 2020 12:00 PM

“1. It was alleged that the facility is not following industry applicable COVID-19 worker protection guidelines from the Centers for Disease Control (CDC) and/or the World Health Organization (WHO), specifically with regards to the following conditions in the lower level through third floor: a. It wa... See Mores alleged that the company is not screening patients or employees; b. It was alleged that the company is not enforcing the use of face coverings for all management and doctors; and c. It was alleged that the company is not enforcing social distancing.

Alleged Hazards: 1, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-06-23
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, New Bedford Sports Club, 1790 Acushnet Ave, New Bedford, MA 02745, USA

New Bedford Sports Club, 1790 Acushnet Ave, New Bedford, MA 02745, USA

November 25, 2020 12:00 PM

“The wearing of face masks, covering the mouth and nose, is not being enforced to help minimize spread of COVID19. Workers are not being instructed and policy enforced, to maintain at least a 6 foot distance in all directions from other workers and customers. Staff who traveled out of state and retur... See Morened to work, did not follow the Massachusetts State requirements for COVID 19 testing and/or 14 day quarantine. Some staff members returned to work and later tested positive for COVID19 potentially exposing people to COVID19.

Alleged Hazards: 3, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-10-15
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Champlain Valley Equipment, Inc., 72 Kubota Drive, Berlin, VT 05602, USA

Champlain Valley Equipment, Inc., 72 Kubota Drive, Berlin, VT 05602, USA

November 25, 2020 12:00 PM

“Hazard Description: Employee's spouse alleges that another employee's spouse tested positive for COVID-19 and that no COVID-19 safety protocols were followed by the employer. Location: Berlin Vermont Store


Source: Osha.gov | Receipt Date: 2020-11-07 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Empire Optical, Varna Avenue, North Hollywood, CA 91605, USA

Empire Optical, Varna Avenue, North Hollywood, CA 91605, USA

November 25, 2020 12:00 PM

“CCR, T8, Section 3203(a)(4) & (6) Employer is not enforcing social distancing or the use of facial masks.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-08-05 See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

October 28, 2020 11:00 AM

“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: October 28, 2020
Recall details: Sunstar Americas, Inc. (SAI) is voluntarily... See Morerecalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 6/30/22 – 9/30/22 (see specific lots below) to the consumer level. This product may be contaminated with the bacteria Burkholderia lata.

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, no adverse events have been reported to SAI related to this recall. 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 by 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 are detailed in the link below.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

November 9, 2020 5:00 PM

“Company name: Lohxa, LLC
Brand name: Lohxa
Product recalled: Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free
Reason of the recall: May be contaminated with Burkholderia lata
FDA Recall date: November 09, 2020
Recall details: Lohxa, LLC is voluntarily recalling Chlorhexidine Gluconat... See Moree Oral Rinse USP, 0.12% Alcohol free (NDC:70166-027-15) products bearing an expiration date from 01/31/21 – 03/31/21 (see specific lots below) to the consumer level. This product is sourced and repackaged from Sunstar Americas Inc. who has notified us the product may be contaminated with the bacteria Burkholderia lata.

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, no adverse events have been reported to Lohxa, LLC related to this recall.

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

- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free is distributed in cases each containing 50 unit dose cups. Each case contains a colored label around the lid and body of the case.

The product can be identified by as shown in the images below. Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free was distributed to Nationwide to hospital pharmacies. Lohxa, LLC is notifying its direct customers by Fedex overnight mail, electronic mail, phone call 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 Lohxa, LLC by phone at 1-800-641-5564 or email info@lohxa.com on Monday-Friday from 8am-5pm EST. 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:

- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free, 15 mL (NDC:70166-027-15) LOT/ EXP: T09101A/01/2021 |T08292A/02/2021 |T10011A/02/2021 |M10193A/03/2021 |T10223A/03/2021

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

November 23, 2020 2:00 PM

“Company name: Fusion Health and Vitality LLC
Brand name: CORE, Immune Boost
Product recalled: CORE essential nutrients and Immune Boost Sublingual Vitamin D3
Reason of the recall: Unapproved new drug
FDA Recall date: November 23, 2020
Recall details: Fusion Health and Vitality LLCis voluntaril... See Morey recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune Boost Labeling was found to contain statements that caused it to become and unapproved new drug under FDA labeling laws. Hordenine HCl is possibly unsafe when taken by mouth. Hordenine HCl might have similar stimulant effects and side effects such as rapid heart rate and high blood pressure.

Fusion Health and Vitality LLC has not received any reports of adverse events related to this recall.  Please review the attached photos for identification. We began shipping Core Essential Nutrients on 1/2/2020 and we began shipping Immune Boost Sublingual Vitamin D3 on 4/15/2020. Both products are packaged with labels which prominently display the product name.  CORE essential nutrients are found in a dark colored jar, in powdered format. 

This product was formulated to mix into a liquid before consumption. The Immune Boost sublingual was packaged in a 2 ounce bottle that came with a sublingual application dropper. Fusion Health and Vitality is notifying its customers by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using it and return it to Fusion Health and Vitality for destruction. Consumers with questions regarding this recall or how to return recalled product can contact Fusion Health and Vitality by calling 1-888-964-5327, 9am to 5pm, Monday Thru Friday, EST. 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.

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
See Less
Reported By SafelyHQ.com User

They do not report positive COVID cases, In-N-Out Burger Distribution Center, Hamburger Lane, Baldwin Park, CA, USA

In-N-Out Burger Distribution Center, Hamburger Lane, Baldwin Park, CA, USA

October 31, 2020 12:15 AM

“I am a Butcher for the In N Out Meat Department in Baldwin Park. They do not report positive COVID cases. They just recently began social distance. Supervisor and managers and associates are covid positive or with symptoms. One associate has lost his sister to covid. He was never quarantined. In n o... See Moreut burger is responsible for a big part in the spread of the virus all across California. See Less
Reported By SafelyHQ.com User

November 19, 2020 6:01 PM

“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi USA
Product recalled: Dexmedetomidine HCL in 0.9% Sodium Chloride Injection
Reason of the recall: Cross Contamination with Lidocaine
FDA Recall date: November 19, 2020
Recall details: Fresenius Kabi USA is voluntarily recalling a singl... See Moree lot of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to a trace amount of lidocaine present in the lot. This recall is being performed to the user level. To date, no adverse drug experience reports have been received for the recalled lot. Administration of Dexmedetomidine HCl containing trace amounts of lidocaine to a patient with lidocaine allergy could result in a potentially life-threatening allergic reaction. 

Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection is approved for intravenous use and indicated for sedation of non-intubated patients prior to and/or during surgical and other procedures. Listed below is a table of the recalled lot distributed nationwide to wholesalers, distributors, hospitals and pharmacies between April 9, 2020 and April 13, 2020. An image of the label is also included below.

- Dexmedetomidine HCl in 0.9%. Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL fill in a 50 mL vial. NDC Number: 63323-671-50. Product Code: 671050. Batch number: 6123925. Expiration Date: 03/2022. First Ship Date: 04/09/2020. Last Ship Date: 04/13/2020

Fresenius Kabi is notifying its distributors and customers by letter and asking them to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product.

Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing any affected lots, and to return the product to Fresenius Kabi.

Customers with questions regarding this recall may contact Fresenius Kabi at 1-866-716-2459 Monday through Friday, during the hours of 8:00 a.m. to 5:00 p.m. Central Time. Consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using this drug product.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

October 28, 2020 10:00 PM

“Company name: Whole Foods Market
Brand name: Whole Foods Market
Product recalled: Macaroni and Cheese products
Reason of the recall: Undeclared egg
FDA Recall date: October 28, 2020
Recall details: Whole Foods Market is voluntarily recalling select prepared Macaroni & Cheese products from store... See Mores across five states because they contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.

The affected products were sold at Whole Foods Market stores in Maryland, New Jersey, Pennsylvania, Virginia and Washington, D.C. The product was sold in plastic containers and in family-style meal kits with Whole Foods Market scale labels in the prepared foods department, available both hot and refrigerated. The product was also available from the chef’s case counter and from Whole Foods Market online and catering menus. The affected products can be identified by the following information. All affected product has been removed from store shelves. No allergic reactions have been reported to date.

- Macaroni & Cheese, chef’s case. Product Code (begins with) M: 286501. Best by 10/28/2020
- Macaroni & Cheese, packaged. Product Code (begins with) M: 263608. Best by 10/27/2020
- Macaroni & Cheese, online and catering. Product Code (begins with) M: 114449 | 109866. Best by 10/23/2020
- Rotisserie Chicken Meals with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 261596 | 261580 | 261590 | 261601 | 261608 | 261616. Best by 10/26/2020
- Fried Chicken Meal with Mac & Cheese, packaged. Product Code (begins with) M: 247257. Best by 10/25/2020
- Fried Chicken Meal with Mac & Cheese, packaged on hot bar. Product Code (begins with) M: 237444. Best by 10/24/2020
- Chicken Rustico Romano Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 241442. Best by 10/28/2020
- Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 299430. Best by 10/28/2020
- BBQ Turkey Meatballs Chef Plate with Mac & Cheese and Green Beans, packaged. Product Code (begins with) M: 241464. Best by 10/28/2020
- Roasted Turkey Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 242019. Best by 10/28/2020

Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

November 15, 2020 8:18 PM

“They are practically forcing people to put hand sanitizer on their hands even though they are not required to do so. I am allergic to some of the stuff because I don't know what's in their hand sanitizer and my hands got all cracked and chapped. They still practically forced people to do it even tho... See Moreugh there's no law. See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Commodore Homes of Indiana, 1902 Century Drive, Goshen, IN 46526, USA

Commodore Homes of Indiana, 1902 Century Drive, Goshen, IN 46526, USA

November 18, 2020 12:00 PM

“They are having employees go back to work that have tested positive for COVID-19 before they have completed quarantine. The employees returning to work who have tested positive are exposing other employees. They are threatening their jobs if they do not go back. They are not letting employees know w... See Morehich departments have tested positive. They have over 10 employees that have tested positive for COVID-19. The mudding department had employees test positive. They shut down the mudding department for 14 days but most of the employees had to come back after 5 days. They have had employees in the cabinet deptartment, the roof department, and the final department that tested positive and they have not shut down. Some employees have tested positive and they pointed them out and fired them. They do not always use safety nets while they are up on the roof, employees are not tied off when they are on the roof.


Source: Osha.gov | Receipt Date: 2020-06-26
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Quandel Group, 224 Wyoming Ave, Scranton, PA 18503, United States

Quandel Group, 224 Wyoming Ave, Scranton, PA 18503, United States

November 25, 2020 12:00 PM

“1) Several employees at the job site have tested positive for the corona virus. The GC is not taking steps to ensure the safety of the workers, including enforcing social distancing and the use of face coverings.


Source: Osha.gov | Receipt Date: 2020-10-26 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walmart Supercenter, 1807 West Craig Road, North Las Vegas, NV 89032, USA

Walmart Supercenter, 1807 West Craig Road, North Las Vegas, NV 89032, USA

November 10, 2020 12:00 PM

“1. Employees are concerned about a rotten egg smell emanating from the deli/bakery area. Employees have reported headaches after working in the area. HAZARD LOCATION: Deli and bakery area. 8/18/2020 JH

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-08-12 See Less
Reported By SafelyHQ.com User