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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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Sonic

Updated: January 7, 2021 12:00 PM

January 7, 2021 12:00 PM

“3 individuals at Sonic in La Plata county tested positive for Covid-19. The outbreak began on 12/15/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Sonic Drive-In, 4561 S 4000 W, WEST VALLEY CITY, UT, 84120, USA

Sonic Drive-In, 4561 S 4000 W, WEST VALLEY CITY, UT, 84120, USA

December 30, 2020 12:00 PM

“1. Manager and employees do not wear mask (COVID-19) as required by UOSH Emergency Rule R614-1.5(F).


Source: Osha.gov | Receipt Date: 2020-11-30 See Less
Reported By SafelyHQ.com User

2 employees tested positive for Covid-19, Sonic Drive-In, 6420 W, Central Ave SW, Albuquerque, NM 87105, United States

Sonic Drive-In, 6420 W, Central Ave SW, Albuquerque, NM 87105, United States

December 29, 2020 12:00 PM

“Multiple employees(2) at SONIC DRIVE-IN in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/30/2020,

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

December 22, 2020 12:00 PM

“Multiple employees(2) at SONIC DRIVE-IN in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/23/2020,

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

December 17, 2020 12:00 PM

“3 individuals at Sonic in La Plata county tested positive for Covid-19. The outbreak began on 12/15/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Sonic Drive-In, 406 West 800 North, OREM, UT, 84057, USA

Sonic Drive-In, 406 West 800 North, OREM, UT, 84057, USA

December 8, 2020 12:00 PM

“Employees not wearing face masks as required for COVID-19

Alleged Hazards: 1, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-11-13 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Sonic Drive-In, 131 Myers Street, CARTHAGE, TN, 37030, USA

Sonic Drive-In, 131 Myers Street, CARTHAGE, TN, 37030, USA

December 8, 2020 12:00 PM

“1. Employees are not being protected from potential exposure to COVID-19. 2. Employees who have tested positive for, or are displaying symptoms of, COVID-19 are allowed to continue working.


Source: Osha.gov | Receipt Date: 2020-11-03 See Less
Reported By SafelyHQ.com User

November 25, 2020 12:00 PM

“Multiple employees(2) at SONIC DRIVE-IN in CLOVIS, 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 21, 2020 12:00 PM

“1 Additional individual at Sonic Drive In in Alamosa county tested positive for Covid-19. The outbreak began on 10/28/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

November 17, 2020 12:00 PM

“Multiple employees(2) at SONIC DRIVE-IN in DEMING, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 11/18/2020,

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

Recent Interesting Reports

January 14, 2021 8:51 PM

“I am a teacher and am authorized to get the Moderna vaccine. I made an appointment in Ridgewood 2 days ago. Appoint was at 5:20 but didn't get my shot until 7:40. The lines are extremely long at night. But the nurse said they are empty in the morning. Once you get inside it is very fast, everyone is... See Morevery helpful and you can sign up for your second vaccine. They make you wait 15 mins to make sure you're ok before you leave. I have no side effects from the shot and feel fine. 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

January 4, 2021 10:32 PM

“Totally false advertising. I order two chainsaws and got two open 26" chains with straps on both ends. Not happy. This advertising was misleading and took over 30 days to receive this product in the mail. I am totally dissatisfied with this purchase and company. 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 7, 2021 1:49 PM

“BlackCass. I ordered a hand-held saw and received only an extra chain. Can I get a refund? See Less
Reported By SafelyHQ.com User

January 14, 2021 11:44 AM

“I wonder how many people were duped by this disreputable company! Guess I should know better than to order from a company I know nothing about! Shame on them for taking hard earned money during this day and time. And shame on Facebook for allowing them to advertise. 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

December 23, 2020 10:00 PM

“Company name: Shane Erickson, Inc. DBA Innovative Marketing Consultants
Brand name: IMC
Product recalled: Wash-Free Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: December 23, 2020
Recall details: Shane Erickson, Inc. is voluntarily recalling lot 2020/05/11 and MFG:... See More2020/05/10 L/N: 20200510-3 of imc Wash-Free Hand Sanitizer 50 ml, 100 ml, 300 ml and Wash Free Hand Sanitizer 300 ml lot 2020/05/11 and Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml lot 2020/05/11 listed in the table below to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).

Risk Statement: 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 accidentally 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, Shane Erickson, Inc. has not received any reports of adverse events related to the product(s) of this recall. Recalled Products:

- IMC Wash-Free Hand Sanitizer 50 ml, 1.7 oz (8 19845 00597 8). Lot: 43962. Expiration date: 45056
- IMC Wash-Free Hand Sanitizer 100 ml, 3.4 oz (8 19845 00598 5). Lot: MFG: 2020/05/10 L/N: 20200510-3. Expiration date: N/A
- IMC Wash-Free Hand Sanitizer | Wash-Free Hand Sanitizer | Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml, 10.14 oz (8 19845 00599 2). Lot: 43962. Expiration date: 45056

The product is used as a hand sanitizer for handwashing to decrease bacteria on the skin when soap and water are not available. All products are packaged in a plastic bottle. The 50 ml are in a HDPE opaque white bottle with a blue cap, the 100 ml is in a clear PET bottle with a clear cap and the 300 ml are in a clear PET bottle with a black pump. The product can be identified by checking the product size, UPC details, lot number and expiration date on the bottle containing the product. The product can also be identified by this information on the back label: Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, YUEWEIXIAOZHENGZI (2020) - 04 - No. 0023.

Some of the product has custom front labels (see examples below) the back label on the custom labels have the same identification information as previously mentioned above. The hand sanitizer was distributed Nationwide in the USA to wholesale and retail customers.

Shane Erickson, Inc. is notifying its distributors and customers by mail/email and is arranging for the return of all recalled products. Consumer, distributors, and retailers that have product, which is being recalled, should stop use or distribution and return to place of purchase. Consumers with questions regarding this recall can contact Shane Erickson, Inc. by phone at 952.252.1254 [Call: 952.252.1254] or email sales@imcsuccess.com Monday through Friday from 8:00 am to 5:00 pm Central Time Zone.

Check the full recall details on fda.gov

Source: FDA
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

The COVID vaccine, London, UK

Symptoms: Other Headache Fever
London, UK

January 11, 2021 10:53 PM

“I got the Oxford vaccine yesterday and I got a bit of a headache but then I went home and slept for most of the night and woke up with a migraine. Also, I had a fever from it. See Less
Reported By SafelyHQ.com User