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Walmart Supercenter, 2240 West Dekalb Street, Camden, South Carolina 29020, USA

Total all time reports:  1
Latest report: October 13, 2020 12:00 PM

Covid-19 OSHA Complaint

October 13, 2020 12:00 PM

“(1) A COVID-19 pandemic plan has not been developed and implemented for employees to include employee wellness checks, disinfecting and sanitizing, social distancing, personal protective equipment, employee return to work and employee training. A manager tested positive for Covid19 and was coming in... See Moreto the store every day of that week.


Source: Osha.gov | Receipt Date: 2020-06-24
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Reported By SafelyHQ.com User

Related Reports

November 25, 2020 12:00 PM

“An employee(1) at WALMART DISTRIBUTION CTR in LOS LUNAS, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 11/25/2020,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

November 25, 2020 12:00 PM

“An employee(1) at WALMART SUPERCENTER in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 11/25/2020,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Premier Healthcare of California, 405 South Street, Redding, CA 96001, USA

Premier Healthcare of California, 405 South Street, Redding, CA 96001, USA

November 25, 2020 12:00 PM

“3203: Employees not being protected from Covid-19.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-05 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Frontier Communications, 1441 North Colony Road, Meriden, CT 06450, USA

Frontier Communications, 1441 North Colony Road, Meriden, CT 06450, USA

November 25, 2020 12:00 PM

“Company heavy duty vans, bucket trucks and pick up trucks are re assigned without COVID-19 decontamination protocols being followed when an employee calls out sick with COVID-19 like symptoms (prior to a positive finding). Disinfecting sprays and or wipes are not provided to employees to clean their... See Morecompany vehicles before during and at the end of shifts.

Alleged Hazards: 2, Employees Exposed: 50
Source: Osha.gov | Receipt Date: 2020-10-29
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Reliant Realty, 55 Richman Plaza, Bronx, NY 10453, USA

Reliant Realty, 55 Richman Plaza, Bronx, NY 10453, USA

November 25, 2020 12:00 PM

“Employer is failing to protect their employees from health hazards associated with potential COVID-19 exposures: 1. Lack of social distancing enforced throughout the office 2. Offices are not cleaned or disinfected 3. Employees enter work area without health prescreening or temperature checks 4. Sta... See Moreff uses the same bathroom (one after the other) without cleaning or cleaning supplies available. 5. Staff uses the copiers, shredders or other shared office equipment without cleaning or sanitizing supplies made available. 6. Staff is required to interact in close proximity to clients without means of protection from potential COVID-19 exposures.

Alleged Hazards: 6, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-08-12
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Reata Cattle Feeders, Marjorie Avenue, Brawley, CA, USA

Reata Cattle Feeders, Marjorie Avenue, Brawley, CA, USA

November 25, 2020 12:00 PM

“T8 CCR 3203(a)(6) Employer does not enforce; social distance and use of face covering in the workplace.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-16 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Vision Performance Optometric Center, 17411 Irvine Boulevard, Tustin, CA 92780, USA

Vision Performance Optometric Center, 17411 Irvine Boulevard, Tustin, CA 92780, USA

November 25, 2020 12:00 PM

“1. T8 CCR § 3203(a)(6) ¿ Facial coverings order not enforced in the workplace. Employees concerned with potential exposure to Covid-19 in the facility. 2. T8 CCR § 3362 ¿ Cockroaches in the workplace.

Alleged Hazards: 2, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2020-10-19 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, CA Department of State Hospitals-Coalinga, 24511 W Jayne Ave, Coalinga, CA 93210, USA

CA Department of State Hospitals-Coalinga, 24511 W Jayne Ave, Coalinga, CA 93210, USA

November 25, 2020 12:00 PM

“1. GISO §5199(g)(6)(B): The employer is failing to ensure that employees assigned to work in the COVID-19 treatment units have been fit tested for their respirators.


Source: Osha.gov | Receipt Date: 2020-08-27 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Factory OS, 1245 Nimitz Ave, Vallejo, CA 94592, USA

Factory OS, 1245 Nimitz Ave, Vallejo, CA 94592, USA

November 25, 2020 12:00 PM

“The employer did not maintain an effective Injury and Illness Prevention Program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not ens... See Moreure masks or other personal protective equipment are being properly used, T8 CCR 3203(a)(4)(6). 2. The employer did not implement physical distancing guidelines. T8 CCR 3203(a)(6). Employees are not given proper personal protective equipment for tasks being completed. Employees working on top of modular units which will occasionally have no temporary guard railing. 3. The employer did not furnish employees with the proper personal protective equipment required for the task, T8 CCR 3380(f)(1)(A)(B)(C). 4. The employer did not ensure guard railing is installed while working from an elevated position, T8 CCR 3210(a).

Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-15
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Los Altos Sub-Acute and Rehabilitation Center, 809 Fremont Avenue, Los Altos, CA 94024, USA

Los Altos Sub-Acute and Rehabilitation Center, 809 Fremont Avenue, Los Altos, CA 94024, USA

November 25, 2020 12:00 PM

“Potential concern regarding implementing Center for Disease Control (CDC), Local Health Department and Cal/OSHA Guidance on Requirements to Protect Workers from Coronavirus to prevent the spread between person-to-person and close contact (within about 6 feet) while sanitizing/cleaning of facility an... See Mored enforce wearing of face covering by all employees. Title 8 CCR Sections 3203, 3380 & 5199.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-02
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Reported By SafelyHQ.com User

Recent Interesting Reports

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
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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
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Reported By SafelyHQ.com User

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
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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

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
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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
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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

Covid-19 OSHA Complaint, Salem Kidney Center, 2705 Boulder Park Court, Winston-Salem, NC 27101, USA

Salem Kidney Center, 2705 Boulder Park Court, Winston-Salem, NC 27101, USA

November 10, 2020 12:00 PM

“Employees could have been exposed to the COVID-19 virus in the workplace, due to employees not being informed when the first employee tested positive for the virus. The number of employees testing positive is increasing, yet employees with symptoms are still being told to come to work.


Source:... See MoreOsha.gov | Receipt Date: 2020-10-23 See Less
Reported By SafelyHQ.com User

November 4, 2020 12:00 PM

“Additional 3 employees confirmed positive for Covid-19 at J. Frank Schmidt & Son Co. in Clackamas County. Investigation Start Date: 7/28/2020 , with the most recent onset of: 10/23/2020 New Cases of: 3

Source: www.oregon.gov See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Target Distribution Center, Archer Drive, Chambersburg, PA 17202, USA

Target Distribution Center, Archer Drive, Chambersburg, PA 17202, USA

November 25, 2020 12:00 PM

“There have been 11 positive Covid-19 cases within the facility during the past week. The employer has not implemented good infection control housekeeping practices of regularly cleaning and disinfecting surfaces, equipment, and other elements of the work environment. Refer to the Centers for Disease... See MoreControl CDC guidance for employers at this link. cdc.gov OSHA in coordination with the Department of Health and Human Services has prepared Guidance on Preparing Workplaces for COVID-19. It can be found here: osha.gov OSHA has Guidance on Returning to Work osha.gov

Alleged Hazards: 1, Employees Exposed: 750
Source: Osha.gov | Receipt Date: 2020-11-03
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Reported By SafelyHQ.com User