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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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Covid-19 OSHA Complaint, Rowan Transport Inc., 2126 Hilltop Mall Road, RICHMOND, CA, 94806, USA

February 10, 2021 12:00 PM

2126 Hilltop Mall Road, Richmond, 94806 California, United States

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 ensure that high touch surfaces in shared vehicles are properly disinfected prior to employee changes, T8 CCR 3205(c)(8)(C).

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-21

Reported By SafelyHQ.com User

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Covid-19 OSHA Complaint, Outback Steakhouse, 521 North Stephanie Street, HENDERSON, NV, 89014, USA

Outback Steakhouse, 521 North Stephanie Street, HENDERSON, NV, 89014, USA

February 24, 2021 12:00 PM

“1. The employer is not complying with the Governor's COVID-19 mandate in regard to following CDC guideline for employees who test positive for COVID-19. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to requiring employees to stay home if symptomatic. 3. The employer... See Moreis not complying with the Governor's COVID-19 mandate in regard to immediately isolating and seeking medical care for individuals who develop symptoms while at work. HAZARD LOCATION: Throughout 10/07/2020 KR

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-09-23
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Covid-19 OSHA Complaint, Marshall Retail Group, 3755 West Sunset Road, LAS VEGAS, NV, 89118, USA

Marshall Retail Group, 3755 West Sunset Road, LAS VEGAS, NV, 89118, USA

February 24, 2021 12:00 PM

“1. The employer is not complying with the Governor's COVID-19 mandate in regard to employees wearing face coverings. Employees in the corporate office do not wear face coverings at all time. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to social distancing between... See Moreemployees. The new desks have been arranged to be closer to each other after the office was remodeled, preventing employees from maintaining a 6 feet distance from each other. 3. There are no hand sanitizers and the soap dispensers are empty, preventing employees from frequently cleaning or disinfecting their hands throughout the day to prevent the spread of COVID-19. HAZARD LOCATION: Office and warehouse. 10/22/2020 KR


Source: Osha.gov | Receipt Date: 2020-10-06
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Covid-19 OSHA Complaint, Valley Business & Tax Services, 3180 West Sahara Avenue, LAS VEGAS, NV, 89104, USA

Valley Business & Tax Services, 3180 West Sahara Avenue, LAS VEGAS, NV, 89104, USA

February 24, 2021 12:00 PM

“1. Employees are concerned with working in an area where the noise level is to high from demolition of concrete floors in the office. HAZARD LOCATION: Inside suite C16 hallway next to front lobby 10/22/2020 KR

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-08 See Less
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Covid-19 Vaccine Experience Notifications

Covid-19 OSHA Complaint, Golden Nugget Las Vegas Hotel & Casino, 129 East Fremont Street, LAS VEGAS, NV, 89101, USA

Golden Nugget Las Vegas Hotel & Casino, 129 East Fremont Street, LAS VEGAS, NV, 89101, USA

February 24, 2021 12:00 PM

“1. Employees are being required to wear face mask in accordance with the Governor's mask mandate however it is extremely hot in the establishment with no air conditioning and there is no air circulating. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to persons/patro... See Morens wearing face coverings while in the Employer's establishment. Employees advise guest that they are required to wear a face mask however the security doesn't back up the employees and remove persons/patrons who refuse to wear a face mask or do so properly. The security team has advised employees that persons/patrons are not required to assure that their nose is covered by their face mask. 3. The employer is not complying with the Governor's COVID-19 mandate in regard to social distancing between employees and the public. There is no social distancing from the sports book area, all the way down the Fremont side of the building especially any time after 3pm on Mondays and weekends. HAZARD LOCATION: Throughout. 10/23/2020 KR

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-14
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Covid-19 OSHA Complaint, Flamingo Las Vegas Operating Company, LLC, 3555 South Las Vegas Blvd., LAS VEGAS, NV, 89109, USA

Flamingo Las Vegas Operating Company, LLC, 3555 South Las Vegas Blvd., LAS VEGAS, NV, 89109, USA

February 24, 2021 12:00 PM

“1. The employer is not disinfecting surfaces that are used often. Employees are concerned about exposure to the COVID-19 virus. HAZARD LOCATION: Throughout the casino floor. 10/26/2020 KR


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Covid-19 OSHA Complaint, Bizport LTD, 9 North 3rd Street, RICHMOND, VA, 23219, USA

Bizport LTD, 9 North 3rd Street, RICHMOND, VA, 23219, USA

February 24, 2021 12:00 PM

“The employer is not implementing precautions to protect employees from contracting and spreading the Coronavirus (COVID-19) in the workplace: a) The wearing of face masks/covering is not enforced. b) Social distancing is not being enforced. c) Employees were not notified of a COVID-19 positive case... See Morein the workplace. d) After an employee tested positive for COVID-19, the facility was not cleaned and disinfected.

Alleged Hazards: 4, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-01-20
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Covid-19 OSHA Complaint, AARP Senior Employment Services, 1806 Chantilly Street, RICHMOND, VA, 23230, USA

AARP Senior Employment Services, 1806 Chantilly Street, RICHMOND, VA, 23230, USA

February 24, 2021 12:00 PM

“The employer is not implementing precautions to protect employees from contracting and spreading the Coronavirus (COVID-19) in the workplace: a) Administrative and work practice controls are not in place to allow for adequate social distancing within the office. b) Adequate administrative and work p... See Moreractice controls were not in place to prescreen or survey employees prior to the commencement of work. c) Common and shared workspaces were not cleaned and disinfected in accordance with the Virginia Department of Labor's Emergency Temporary Standard §16VAC25-220. d) The wearing of face masks/covering is not enforced.

Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-01-14
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An Employee test positive for Covid-19, GRTC Transit System, 301 E Belt Blvd, Richmond, VA 23224, United States

GRTC Transit System, 301 E Belt Blvd, Richmond, VA 23224, United States

February 21, 2021 12:00 PM

“An employee at GRTC Transit System located on E Belt Blvd in Richmond recently tested positive for Covid-19.

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Covid-19 OSHA Complaint, AC Transit District, 2016 Macdonald Avenue, RICHMOND, CA, 94801, USA

AC Transit District, 2016 Macdonald Avenue, RICHMOND, CA, 94801, USA

February 17, 2021 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 to exclude employees who have been exposed to COVID-19 Cases by giving negative attendance marks for missing work, T8 CCR 3205(c)(10)(B). 2. The employer did not ensure employees can maintain a physical distance of at least 6 feet between other persons, T8 CCR 3205(c)(6). 3. The employer did not ensure that proper markings of visual ques are installed in so patrons are aware of the physical distancing standards, T8 CCR 3205(c)(6).

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Covid-19 OSHA Complaint, HopeBridge Autism Therapy Center, 3771 S A St, RICHMOND, IN, 47374, USA

HopeBridge Autism Therapy Center, 3771 S A St, RICHMOND, IN, 47374, USA

February 16, 2021 12:00 PM

“They are letting clients in the building with flu like symptoms, they are letting clients in with fevers, they are trying to put two clients with one therapist because they are short staffed.


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Recent Interesting Reports

February 16, 2021 11:55 PM

“The FSA announced the recall of Boots Multivitamins supplements by Boots because they have been incorrectly packed with multivitamins containing iron. This resulted in vitamin K not being present within the supplement and iron incorrectly added to the supplements instead. Iron has not been mentioned... See Moreon the label. This means the product is a possible health risk to individuals who may also be consuming iron supplements in addition to these multivitamins.

FSA advises consumers to stop taking the multivitamin supplements. Instead, return it to the Boots store from where it was bought for a full refund. This recall affects multivitamins sold between 12 and 19 January 2021 only.

- Boots Multivitamins (180 tablets). Item code: 80 57 311. Batch code: 1805 and 1806. Best before: end of November 2022.

This product does not contain vitamin K but does contain iron. Excess supplemental iron can result in gastrointestinal effects such as pain, discomfort, constipation or nausea and vomiting.

Check the full recall details on the FSA website food.gov.uk
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February 7, 2021 11:58 PM

“The FDA observed the website offers “Corona Destroyer Tea” for sale in the United States in two options, “Prevention” and “Reversal,” and that this product is intended to mitigate, prevent, treat, diagnose, or cure COVID-19[1] in people.

Based on FDA review, this product is an unapproved new dr... See Moreug sold in violation of section 505(a) of the Federal Food, Drug, and Cosmetic Act (FD&C Act), 21 U.S.C. § 355(a). Furthermore, this product is a misbranded drug under section 502 of the FD&C Act, 21 U.S.C. § 352. The introduction or delivery for introduction of this product into interstate commerce is prohibited under sections 301(a) and (d) of the FD&C Act, 21 U.S.C. § 331(a) and d. Some claims on the website and product label establish the intended use of the product and misleadingly represent it as safe and/or effective for the treatment or prevention of COVID-19

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February 17, 2021 6:09 PM

“A scam regarding a small knock-off chain saw that is the center of a scam by Blackcass of Houston, TX or LA, CA or probably China somewhere. We ordered a Blackcass 2020 Hot selling GTA 26 Battery-Powered Wood Cutter X 1 in December 2020. We did received, via USPS, a 25" long segment of chain saw l... See Moreinks with Orange handles on each end, so it is NOT Battery-Operated. One of the photos in the Blackcass ad that are associated with this SCAM are EXACTLY the same photo used by the very legitimate Stihl company model GTA-26...only the word, "Stihl" is omitted on the Blackcass ad's photo. So, consumers and the real manufacturer are BOTH being scammed. See Less
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Covid-19 Vaccine Experience Notifications

January 27, 2021 9:01 PM

“Company name: Meitheal Pharmaceuticals, Inc.
Brand name: Meitheal Pharmaceuticals, Inc.
Product recalled: Cisatracurium Besylate Injection, USP 10mg per 5mL
Reason of the recall: Mislabeling
FDA Recall date: January 27, 2021
Recall details: Meitheal Pharmaceuticals, Inc. (“Meitheal”), annou... See Morenced today that it is voluntarily recalling one (1) lot of Cisatracurium Besylate Injection, USP 10mg per 5mL to the user level. The decision to recall the product was made after a product complaint revealed that a portion of Lot C11507A of cartons labeled as Cisatracurium Besylate Injection, USP 10mg per 5mL, containing 10-vials per carton, contained 10-vials mis-labeled as Phenylephrine Hydrochloride Injection, USP 100mg per 10mL. 

To date, Meitheal has not received reports of any adverse events or identifiable safety concerns attributed to the lot. There is a reasonable probability that a patient who requires cisatracurium for muscle paralysis as part of general anesthesia is administered phenylephrine instead would not receive any skeletal muscle relaxation and could cause a hyperadrenergic state resolution in elevated blood pressure, arrhythmia and cardiac/brain ischemia.  If this is not quickly diagnosed and treated, severe illness or death can occur. 

There is a reasonable probability that a patient who requires phenylephrine to increase their blood pressure, such as patients with severely low blood pressure, especially resulting from septic shock who is administered cisatracurium instead could result in a fast onset of muscle paralysis and decrease in oxygen. If this is not quickly diagnosed and treated, severe illness or death can occur within minutes. Cisatracurium Besylate Injection is used as a nondepolarizing neuromuscular blocker. 

The affected Cisatracurium Besylate Injection lot being recalled is C11507A, EXP. October 2021.  The product can be identified as a 5mL vial stoppered with a rubber stopper and sealed with aluminum seal having an Aqua color flip-off seal.  Meitheal commenced shipping the product to customers on August 19, 2020 which was distributed to wholesalers nationwide in the USA.

- Cisatracurium Besylate Injection, USP 10mg per 5mL. Lot Number: C11507A*. Expiration Date: October 2021*. NDC Number: 71288-712-06 (unit of sale) |71288-712-05 (unit of use). Distribution Dates: August 19, 2020 – January 04, 2021.

*Note: Mis-labeled product will have this same Lot Number of C11507A and Expiration Date of October 2021 but will be labeled on the vial as Phenylephrine Hydrochloride Injection, USP 100mg per 10mL, NDC 71288-808-77 (unit of use).

Meitheal has notified its distributors and customers in writing to arrange for return of all recalled product. Customers who have purchased the product should not open the carton or use its contents and should immediately quarantine and return the recalled lot of product. Customers who may have further distributed this product should promptly identify their customers and notify them at once of this product recall.

Consumers with questions regarding this recall can contact Meitheal’s Customer Service weekdays 8:00AM to 6:00PM CST at 844-824-8426. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

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, as follows.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

February 3, 2021 1:00 PM

“Company name: Apotex Corp
Brand name: Apotex Corp.
Product recalled: Enoxaparin Sodium Injection, USP
Reason of the recall: Packaging error resulting in incorrect dosage listed
FDA Recall date: February 03, 2021
Recall details: Apotex Corp is voluntarily recalling two (2) batches of Enoxaparin... See MoreSodium Injection, USP to consumer level due to a packaging error resulting in some syringes barrels containing 150 mg/mL markings (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength) on the syringe barrel and vice versa. The packaging error was discovered during a customer complaint investigation. To date, Apotex has not received any reports of adverse events related to use of these two batches. The affected product is manufactured by Gland Pharma Limited, Hyderabad, India.

Health Hazard Assessment: Incorrect syringe barrel marking could lead to miscalculation and inaccurate dose administration to patients. In one recalled batch (batch CS008, strength 100 mg/mL), if a consumer used a 150 mg/mL concentration packaged in a barrel corresponding to a l00 mg/mL concentration, patients could receive 3.75 mg of Enoxaparin, instead of 3 mg of Enoxaparin. In another recalled batch (batch CT003, strength 120 mg/0.8mL), if a consumer used a 100 mg/mL concentration packaged in a barrel corresponding to a 150 mg/mL concentration, patients would receive 2 mg of Enoxaparin rather than 2.5 mg of Enoxaparin. Accidental overdosage following administration of enoxaparin sodium injection may lead to bleeding complications. Alternative, if the dose administered is less than prescribed, the patient may be subject to developing some blood clotting conditions.

Enoxaparin Sodium injection is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE), Treatment of Acute Deep Vein Thrombosis, prophylaxis of ischemic complications of unstable angina and non-Q-wave myocardial infarction, when concurrently administered with aspirin and Treatment of Acute ST-Segment Elevation Myocardial Infarction.

The affected Enoxaparin Sodium Injection, USP can be identified by NDC numbers stated on carton and label of the product.

Product: Enoxaparin Sodium Injection, USP
Batch #: CS008
Strength: 100 mg/mL
Syringe Barrel Measurement Markings: 100 mg/mL
Pack Size: 10 x 1mL Single Dose Syringes
NDC NumberOn Carton: 60505-0795-4
NDC Number On label: 60505-0795-1
UPC Code on Carton: 360505079544
UPC Code on label: (01)10360505079510

Product: Enoxaparin Sodium Injection, USP
Batch # : CT003
Strength: 120 mg/0.8mL
Syringe Barrel Measurement Markings: 150 mg/ mL
Pack Size: 10 x 0.8 mL Single Dose Syringes
NDC NumberOn Carton: 60505-0796-4
NDC Number On label: 60505-0796-0
UPC Code on Carton: 360505079643
UPC Code on label: (01)10360505079602

The two (2) affected batches of Enoxaparin Sodium Injection, USP were distributed by Apotex nationwide in the USA to Wholesalers and Warehousing Chains. Apotex Corp. is currently notifying its affected direct account Wholesalers and Warehousing Chains, via mail (FedEx Standard Overnight) by mailing a recall notification letter and is arranging for return of all recalled product.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

February 19, 2021 5:13 PM

“I choose not to get the injection because as a Big Pharma trained drug rep, realized Pfizer, Moderna, and AZ were only given Emergency’ FDA approval and skipped the animal trials. The jab offers NO immunity nor does it stop transmission; it is therefore NOT a vaccine. It is nothing more than Expe... See Morerimental Biological Agent for a virus with a 99% survival rate (without any intervention. There are much saver therapeutics. He only benefit to the jab is a lessened symptom. The CDC updates the adverse events every Friday. As you can see from their last report, over 900 have already died and over 11,000 have sustained serious injuries.

The risk/return isn’t favorable. It takes about 7 yrs to develop a vaccine. This is way too soon.
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Reported By SafelyHQ.com User

February 23, 2021 1:16 PM

“I ordered the Mini chain saw and the picture on the right is what i got. What the hell am i supposed to do with a chain without the saw. I am on social security and can not afford to give idiots my money. Some bastard out there is getting rich off trusting people. I want my d**n money back or i get... See Morea lawyer. I hate a f*****g thief! See Less
Reported By SafelyHQ.com User

Pfizer Vaccine side effects, Pittsburgh, PA, USA

Symptoms: Headache Soreness Skin Rash
Pittsburgh, PA, USA

February 1, 2021 4:52 PM

“Morning recieved: Arm sore. Headache. Then broke out in welt type hives from my face down to my toes. Had to go to ER for epi pen and steroids. See Less
Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: ER

February 15, 2021 1:00 AM

“I ordered 2 chainsaws from an ad on the internet which popped up while playing cards on my phone from a web company called Blackcass.com. I thought that I was ordering rechargable woodcutter/chainsaws, but received two chains instead. They would not refund my money or allow me to return and get a re... See Morefund. They said that I had ordered the chains when I only see a big picture of a chainsaw. Their website is misleading to say the least. I would say I was scammed. They also scam people on their website with another chainsaw they are selling that has the well known brand name of Stihl on the saw. Then they send you an off brand saw made in China. Fraud indeed! See Less
Reported By SafelyHQ.com User

January 29, 2021 10:45 AM

“The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 43 pounds of not-ready-to-eat (NRTE), heat treated, not fully cooked chicken enchilada products due to misbranding and an undeclared allergen. FSIS is issuing this public... See Morehealth alert out of the utmost of caution to ensure that consumers with allergic reactions to soy are aware that these products should not be consumed. A recall was not requested because the chicken enchilada products are no longer available in commerce.

The NRTE product labeled as “HyVee mealtime CHICKEN ENCHILADAS” was produced on Jan. 3, 2021. The following product is subject to the public health alert: [View Label (PDF only)]

62.4-oz. (3-lbs. 14.4-oz.) heat and serve container of “HyVee mealtime CHICKEN ENCHILADAS” with lot code “21003” and “Best If Use By: 01/10/2021” date on the product label. The products bear establishment number “P51558” inside the USDA mark of inspection. These items were distributed to HyVee retail locations in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.

The problem was discovered when a HyVee retail store employee identified the labeling issue and reported it to the establishment.

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

For more info: fsis.usda.gov

Source: FSIS
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Reported By SafelyHQ.com User