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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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Bojangles

Updated: January 21, 2021 12:00 PM

Covid-19 OSHA Complaint, Bojangles' Restaurants, Inc., 1897 Sandhill Boulevard, ABERDEEN, NC, 28315, USA

Bojangles' Restaurants, Inc., 1897 Sandhill Boulevard, ABERDEEN, NC, 28315, USA

January 21, 2021 12:00 PM

“Employees could be exposed to the COVID-19 virus in the workplace, due to: 1. Some employees with family members, and/or members of their household, who have COVID-19, are continuing to come to work; 2. Employees are not given temperature checks or any kind of health screen/questionnaire when they c... See Moreome to work.


Source: Osha.gov | Receipt Date: 2020-12-01
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Bojangles, 1407 E. 3rd St, CHARLOTTE, NC, 28204, USA

Bojangles, 1407 E. 3rd St, CHARLOTTE, NC, 28204, USA

January 13, 2021 12:00 PM

“There were two employees which were positive for the COVID-19 virus this week. The employer is not cleaning the facility and requiring other employees to continue to report to work.


Source: Osha.gov | Receipt Date: 2020-11-12 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Bojangles, 516 Hampton Street, Kershaw, South Carolina 29067, USA

Bojangles, 516 Hampton Street, Kershaw, South Carolina 29067, USA

August 3, 2020 12:00 PM

“1. The employer has not taken any precautions to limit the spread of COVID-19 such as quarantine employees with the symptoms. A manager has been in contact with someone who tested positive for COVID-19. They are still working and displaying symptoms of the virus.

Source: Osha.gov | Receipt Da... See Morete: 2020-06-25 See Less
Reported By SafelyHQ.com User

July 23, 2020 12:00 PM

“An employee at Bojangles at its Elmsley Square location tested positive for coronavirus this month on Monday July 13. If you visited the restaurant location during that time, please report it and any other location that you visited.


Source: wfmynews2.com See Less
Reported By SafelyHQ.com User

July 21, 2020 12:00 PM

“A Bojangles employee at the Elmsley Square location in Greensboro tested positive for COVID-19

Source: wfmynews2.com See Less
Reported By SafelyHQ.com User

July 6, 2020 12:00 PM

“An employee at Bojangles restaurant at 1402 W. Trade St in Charlotte has tested positive for COVID-19. It is unknown when the employee worked last.

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

June 24, 2020 12:00 PM

“An employee at Bojangle’s fried chicken restaurant on West Main Street in Salem tested positive for COVID-19. The employee last worked on June 15. If you visited the restaurant location during that time, please report it and any other location that you visited.

Source: wdbj7.com See Less
Reported By SafelyHQ.com User

Bojangles' employee tests positive, Bojangles' Famous Chicken 'n Biscuits, 505 Madison Blvd, Roxboro, NC 27573, USA

Bojangles' Famous Chicken 'n Biscuits, 505 Madison Blvd, Roxboro, NC 27573, USA

May 17, 2020 12:00 PM

“An employee of Bojangles on Madison Boulevard has tested positive for COVID-19.
The employee last worked at the restaurant on Tuesday. Bojangles closed the restaurant Wednesday.

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

April 26, 2020 12:00 PM

“An employee at Bojangles' has tested positive for the coronavirus. The employee works at the Main St. location in Lancaster, SC and last worked on Wednesday, April 22nd.

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

Recent Interesting Reports

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... See Moretheir 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.
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Reported By SafelyHQ.com User

January 12, 2021 2:00 PM

“Company name: Midwestern Pet Foods Inc.
Brand name: Sportmix, Nunn Better, ProPac, and Others
Product recalled: Dog and Cat Pet Food
Reason of the recall: Aflatoxin Levels Exceed Acceptable Levels
FDA Recall date: January 11, 2021
Recall details: Company Announcement Midwestern Pet Foods, Inc.,... See Moreof Evansville, IN is expanding its December 30, 2020 voluntary recall of certain dog and cat food products produced in our Chickasha Operations Facility to include all dog and cat pet food products made with corn products because those products may contain aflatoxin levels which exceed acceptable limits. Products were distributed nationally to online distributors and retail stores nationwide. Midwestern Pet Foods is expanding its voluntary recall out of an abundance of caution to help protect the health and safety of pets. The products recalled cover all that expire on or before July 9, 2022, depicted as “07/09/22” in the date code on the product, as discussed below. Products with expiration dates after 07/09/22 are not included in the recall. 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 certain lots of products. No human illnesses have been reported. Out of an abundance of caution, we have expanded this recall to cover all corn products containing pet foods with expiration dates prior to 07/09/22. 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 and best buy date. Lot code information may be found on the back of bag and will appear in a three‐line code, with the top line in format “EXP 03/03/22/05/L#/B###/HH:MM”.

As explained above, this recall covers ONLY product manufactured at Midwestern Pet Food’s Chickasha, Oklahoma facility. Note that the unique Chickasha Facility identifier is located in the date code as a“05” and “REG. OK‐PFO‐0005” at the end of the date code.

In addition, the only Midwestern Pet Foods facility that produces product bearing a three‐line date code is our Chickasha Facility (See first image below).

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 food in a way that children, pets and wildlife cannot access them. Wash and sanitize pet food bowls, cups, and storage containers. Always ensure you wash and sanitize hands after handling recalled food or any utensils which have contacted recalled food. 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 voluntary recall is being conducted in cooperation with the U.S. Food and Drug Administration. All other Midwestern Pet Foods products are unaffected by this recall action. Recalled products are as follows, with lot codes found in Expanded Recall Lot Numbers:

Pro Pac Adult Mini Chunk
Pro Pac Performance Puppy
Splash Fat Cat 32%
Nunn Better Maintenance
Sportstrail 50
Sportmix Original Cat 15
Sportmix Original Cat 31
Sportmix Maintenance 44
Sportmix Maintenance 50
Sportmix High Protein 50
Sportmix Energy Plus 44
Sportmix Energy Plus 50
Sportmix Stamina 44
Sportmix Stamina 50
Sportmix Bite Size 40
Sportmix Bite Size 44
Sportmix High Energy 44
Sportmix High Energy 50
Sportmix Premium Puppy 16.5
Sportmix Premium Puppy 33

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

January 7, 2021 7:57 PM

“I purchased the portable carbon steel chain from Blackcass. When going to their site, It looks like you are getting the Chain saw and are advertising it for $29.99 When in reality you are purchasing the chain for $29.99. They do advertise that you are getting the chain and not the chainsaw, but m... See Moreake it look like you are getting the saw. When you look at the ad it is very deceiving. I do realize that I did not pay attention when I pushed the buy button. They do say 100% money back guarantee, but do not honor that when you try to return the item. I keep contacting the company. First they offered me the saw at a discount price. Second they offered me 10% of my money back. Then 12% then 15% twice. They keep saying that not to return the item until they give me the return address. They have not yet sent me the return address. I have a friend that says they wait to send me the return address until it is too late to send it to them because they give you 30 days to return the item. They have not yet sent me the address. I just want to send it back. I have contacted paypal and they say there is nothing they can do. I have contacted yt network technology which is the company that paypal says I purchased the item from. I have only heard from them 1 time and sent them the information that they asked for, but have not heard back. What do I do? Can this company be stopped? See Less
Reported By SafelyHQ.com User

January 16, 2021 3:36 PM

“I ordered a Stihl wood cutter and got an IWORKS mini chain saw that does not work. See Less
Reported By SafelyHQ.com User

Moderna Covid19 vaccine, New Jersey, USA

Symptoms: Fever Chills Muscle Pain Soreness
New Jersey, USA

January 25, 2021 11:34 PM

“My first Moderna injection gave me minor symptoms. The first 30 min after the injection I felt slight soreness in the injection site. As the day progressed my arm got very sore where it was hard to lift it above my shoulder. Before bed I felt muscle aches and chills. Overnight I got a 101.7 fever wh... See Moreich decreased to 100.6 a few hours later. My temp remained around 100 for several more hours before I took 2 Tylenol tablets. After I took the Tylenol my fever, aches and chills went away, but my arm remained sore for a few more days. See Less
Reported By SafelyHQ.com User

January 25, 2021 11:29 PM

“Moderna Vaccine. I will receive my 2nd dose on 1/28/21 at 3pm. No side effects. Arm mildly sore for 2 days. Pain scale 1 out of 10. Since receiving 1st dose, I have had more energy and been more productive. See Less
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 3:23 PM

“I ordered a Stihl battery powered chainsaw as.shown on the advertisement on Facebook but instead I received a Commando Wire Saw that worked manually. I feel this needs to reported if not made right! The advertisement was very misleading. See Less
Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User

January 25, 2021 7:00 PM

“Company name: Nostrum Laboratories, Inc.
Brand name: Nostrum Laboratories, Inc.
Product recalled: Metformin HCl Extended Release Tablets, USP 750 mg
Reason of the recall: Due to levels of nitrosamine impurities above the ADI limit of 96 ng/day
FDA Recall date: January 25, 2021
Recall details: K... See Moreansas City, Missouri,Nostrum Laboratories, Inc. is voluntarily recalling one lot of Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) to the consumer level. The Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) have been found to contain levels of nitrosamine impurities above the ADI limit of 96 ng/day, as published in the FDA Guidance Document issued September 2020. This is an expansion of the recall initially announced on November 2nd 2020. NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. 

NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables. To date, Nostrum Laboratories, Inc. has not received any reports of adverse events related to this recall.

The product is indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in HDPE bottles of 100 tablets, under NDC 29033-056-01. The affected Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) lot is listed in the table below. The product can be identified as an off-white oblong tablet debossed with “NM7”. Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) was distributed Nationwide in the USA to wholesalers who further distributed to pharmacies and patients.

- Product Description: Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets)
- NDC: 29033-056-01
- Lot Number: MET200601
- Expiry Dates: 07/2022

Nostrum Laboratories, Inc. is notifying its distributors by letter and is arranging for return of all recalled products. Consumers with medical questions regarding this recall can contact Nostrum Laboratories, Inc. Medical Affairs at phone number 816-308-4941 or email quality@nostrumpharma.com Monday through Friday from 8 am – 5 pm CST. Consumers should contact their physician or pharmacy for further medical advice.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User