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Riverside, California, United States

Updated: January 14, 2021 12:00 PM

Covid-19 OSHA Complaint, Manheim Riverside, 6446 Fremont Street, RIVERSIDE, CA, 92504, USA

Manheim Riverside, 6446 Fremont Street, RIVERSIDE, CA, 92504, USA

January 14, 2021 12:00 PM

“T8CCR 3203(a) Employees are not wearing masks or staying 6 feet apart from one another.

Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-11-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, THE RECYCLER CORE COMPANY, 2727 KANSAS AVENUE, RIVERSIDE, CA, 92507, USA

THE RECYCLER CORE COMPANY, 2727 KANSAS AVENUE, RIVERSIDE, CA, 92507, USA

December 30, 2020 12:00 PM

“T8CCR 3203(a)(4) T8CCR 3203(a)(7) Employer is not following guidelines or enforcing Covid-19 requirements.

Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-10-21 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, County of Riverside, 3450 14th St., RIVERSIDE, CA, 92501, USA

County of Riverside, 3450 14th St., RIVERSIDE, CA, 92501, USA

December 30, 2020 12:00 PM

“T8CCR 3203(a)(4) T8CCR 3203(a)(6) Employer not disclosing Covid-19 cases to employees, creating possible exposure to workers entering unknown Covid-19 work areas.

Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-10-18 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Amazon Fulfillment, 20901 Krameria St, RIVERSIDE, CA, 92508, USA

Amazon Fulfillment, 20901 Krameria St, RIVERSIDE, CA, 92508, USA

December 30, 2020 12:00 PM

“T8CCR 3203 Employer not enforcing PPE requirements during Covid-19 outbreak. T8CCR 3203 Employer not enforcing social distancing during Covid-19 outbreak.

Alleged Hazards: 2, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-10-06 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, European Wax Center, 3639 Riverside Plaza Drive, RIVERSIDE, CA, 92506, USA

European Wax Center, 3639 Riverside Plaza Drive, RIVERSIDE, CA, 92506, USA

December 15, 2020 12:00 PM

“T8CCR 3203 Employer not taking temperature/screening for Covid exposure of employees or customers. Not staggering clients to allow for sanitizing between guests.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-21 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, RighTime Home Services Riverside, 3030 Myers Street, Riverside, CA 92503, USA

RighTime Home Services Riverside, 3030 Myers Street, Riverside, CA 92503, USA

November 25, 2020 12:00 PM

“T8CCR 3203 Employees were exposed to another employee with Covid-19. They did not follow CDC guidelines to reopen building. Did not allow employees who felt were exposed to not come to work. The company made it seem like there was no other choice. Employees will now go into customers home and contin... See Moreue to spread this virus to customers in Socal.

Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-06-18
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Immigration Law Offices of Hadley Bajramovic, 5225 Canyon Crest Drive, Riverside, CA 92507, USA

Immigration Law Offices of Hadley Bajramovic, 5225 Canyon Crest Drive, Riverside, CA 92507, USA

November 25, 2020 12:00 PM

“T8CCR 3203 The first incident occurred when CA State was still shut down (first time) due to Covid-19. Offices were barely opening up. Attorney H had gone to Mexico on business, upon her return, she came straight to the office without quarantining herself for 14 days. She had gotten off her plane &... See Morecame into the office, exposing everyone, especially those in the bull pen (open area where most employees sit, that is not socially distant) area to position getting Covid-19. There were about 8 people there in the bull pen area. The second incident occurred on June 30, 2020, Attorney H came in through the door that leads to the bull pen area without a face mask. She was on a zoom meeting on her phone and said, dang I forgot my face mask. Instead of going back out she continued walking thru the bull pen area & through the 2 offices & reception area that lead to her office. She exposed about 12 employees that day. 3 of us employees, sit right next to the door in the bull pen area. She passed by us first.

Alleged Hazards: 2, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-07-14
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Superior Court of California, County of Riverside - Family Law Courthouse, 4175 Main Street, Riverside, CA 92501, USA

Superior Court of California, County of Riverside - Family Law Courthouse, 4175 Main Street, Riverside, CA 92501, USA

November 25, 2020 12:00 PM

“T8CCR 3203 I am writing to you today because I work for the Superior Court of California, County of Riverside. We are currently working in very unsafe condition. We share pens, highlighters, etc that's needed in every day jobs. The Courts have not implemented temperature checks or any other screenin... See Moreg devices. I was allowed back at work with a temperature because it was not checked at the door. I am a previous registered nurse. Everything is wrong at the family law facility located at 4175 Main Street in Riverside. Most of Riverside County has been closed and yet our Presiding Judge Vineyard has left us open.

Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-07-14
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Riverside Comprehensive Treatment Center, 1021 W La Cadena Dr, Riverside, CA 92501, USA

Riverside Comprehensive Treatment Center, 1021 W La Cadena Dr, Riverside, CA 92501, USA

November 25, 2020 12:00 PM

“T8CCR 3203 There are less than 20 staff members working on-site at the facility. Since the start of Covid-19, 5 counselors tested positive and another employee was symptomatic for 10 days while testing negative. Facility not offering hazard pay even though clientele includes high-risk patients with... See Moreunderlying disorders and health conditions (tuberculosis, COPD, diabetes, cancer etc)- current patients and visitors not notified about positive cases or risk of exposure. When the first two positive cases were discovered, HR department and corporate representative had team meeting via phone where they stated 1) hazard pay will not be provided and 2) they could not encourage employees to go get tested because they are not medical practitioners. Prior to positive cases and up until recently, director would make it difficult to assert mandates upon entering the facility (i.e. wearing face covering) by stating that if people do not have symptoms, they can be inside facility without mask.

Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-07-14
See Less
Reported By SafelyHQ.com User

April 5, 2020 12:00 PM

“My Grandmother tested positive for Covid-19. She does not have the common symptoms everyone is looking out for though... It started on March 18th with her throwing up, she had no sense of appetite, and was very weak. These symptoms just sounded like she had the flu. This went on for a few days and... See Morewe asked if she wanted or felt the need to go to the hospital, but she said no. The next day she was very dehydrated & we had asked her if we should call a nurse to come & give her fluids. She said no, but it was to the point we thought it was appropriate to call one anyways. Once the nurse came by she gave my grandma her fix & she began to feel better. However, hours later she was already back to feeling horrible. On March 23rd we took her to the emergency room and nurse came up to us and asked her “do you have a fever? Are you coughing? Are you having troubles breathing?” And she answered all with “No” They took her in and gave her fluids, nausea meds, ran some tests and they noticed the marks on her lungs from having previous years of Pneumonia. Those old marks are the only reason they tested her for Covid-19. We got the results 10 days later that she tested positive. See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

January 4, 2021 7:46 PM

“I ordered a hand held chain saw on Dec 12th 2020. I was v
Charged $40.89 .
What did come in the mail
Was a extra chain, but no saw See Less
Reported By SafelyHQ.com User

Moderna COVID-19 vaccine, Sevierville, TN, USA

Symptoms: Headache Chills Fatigue Joint Pain Muscle Pain Soreness
Sevierville, TN, USA

January 22, 2021 1:14 PM

“Moderna first vaccine 12/23/20. Arm felt sore a little worse than a tetanus shot. Felt pretty fatigued the next two days afterwards. Second Moderna vaccine 01/20/21. Arm felt sore pretty much within a couple of hours. The next day had hot/cold chills, muscle/joint pain and headache. The 2nd day my... See Moreinjection site was red/warm to touch and has spread quite a bit. Showed the Covid screeners and they said that this is common after the 2nd shot. Took Tylenol and will continue to watch. See Less
Reported By SafelyHQ.com User

January 21, 2021 4:42 PM

“I fed both my dogs a chicken wrapped dream See Less
Reported By SafelyHQ.com User

December 31, 2020 11:24 AM

“Responding to an add on facebook I ordered and paid for a battery powered chainsaw on Dec. 13. I then received a confirmation email. On Dec. 30 I received an envelope the size of a cigarette pack containing a manual chainsaw. Where are the fact checkers when you need them? See Less
Reported By SafelyHQ.com User

January 4, 2021 11:39 PM

“I ordered this saw on December 13th, on December 15th I recieved a confirmation notice the my purchase was on its way, today January 4th 2021 in the mail all I recieved was a chain. Is this a scam or what,and where is the rest of my purchased SAW????? See Less
Reported By SafelyHQ.com User

January 8, 2021 12:49 PM

“On December 14, 2020 I ordered the Blackcass battery operated chainsaw. On January 8, 2021 I received a chain with two handles attached. See Less
Reported By SafelyHQ.com User

January 1, 2021 9:01 PM

“Company name: Precision Dose Inc.
Brand name: GUM Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 15 mL unit dose cups
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 31, 2020
Recall details: Company Announcement Precision Dose,... See MoreInc. is voluntarily recalling all lots of Chlorhexidine Gluconate Oral Rinse USP, 0.12%, 15mL Unit Dose Cups bearing an expiration date from 1/31/2021 – 02/28/2022 (see specific lots below) to the consumer level. Precision Dose, Inc. was notified by the manufacturer of the product, Sunstar Americas, Inc., that this product may be contaminated with the bacteria Burkholderia lata.

From information provided by the manufacturer, Sunstar Americas, Inc., 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 pneumonia and bacteremia.

To date, no adverse events have been reported to Precision Dose, Inc. 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 the product impacted is:

- Distributed in cases each containing 3 shrink-wrapped plastic trays each with 10 unit dose cups, 30-pack. NDC 68094-028-62
- Distributed in cases each containing 10 shrink-wrapped plastic trays each with 10 unit dose cups, 100-pack. NDC 68094-028-61

Chlorhexidine Gluconate Oral Rinse was distributed nationwide in the USA to pharmaceutical wholesalers. Precision Dose, Inc. is notifying its consignees directly and is arranging for return of all recalled product. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact Precision Dose, Inc. at 1 (800) 397-9228 (Monday-Friday, 8:00 AM to 4:30 PM Central Time) or by email to customercare@precisiondose.com. Consumers should contact their physician or healthcare provider if they have experienced problems that may be related to using this drug product. Affected products and lot numbers follow below: AFFECTED LOTS-Chlorhexidine Gluconate Oral Rinse USP, 0.12%

Check the full recall details on fda.gov

Source: FDA
See Less
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

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 8, 2021 6:01 PM

“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... See Morelac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.

Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.

Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.

Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019

Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors 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 the affected lot, and to return the product to Fresenius Kabi.

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