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Updated: April 7, 2021 12:00 PM
Southwest Airlines, 8835 Bear Road, ORLANDO, FL, 32827, USA
April 7, 2021 12:00 PM
“see COVID-19 Ltr
Source: Osha.gov | Receipt Date: 2021-02-16 ”
Southwest Airlines Station, 2500 E. Airport Dr., ONTARIO, CA, 91761, USA
March 24, 2021 12:00 PM
“T8CCR 3205.1(b) - Outbreak at work location. 1-4 positive cases on a daily basis. T8CCR 3205.1 (b)(2)(A) - No testing being done. T8CCR 3205(c)(6) - No social distancing.
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-24 ”
Southwest Airlines, 1 Airport Drive, OAKLAND, CA, 94621, USA
March 17, 2021 12:00 PM
“1. The employer failed to ensure that employees wear face coverings and maintain at least six feet of social distance within the break room 21, 24 & 27, and within the cargo bays of the aircrafts. T8 CCR 3205(c)(6)(A) & (c)(7)(A)
Alleged Hazards: 1, Employees Exposed: 1... Source: Osha.gov | Receipt Date: 2021-01-19 ”
Several Employees test positive for Covid-19, Southwest Airlines, 6900 Airport Blvd W, Sacramento, CA 95837, United States
Southwest Airlines, 6900 Airport Blvd W, Sacramento, CA 95837, United States
February 11, 2021 12:00 PM
“Several employees at Southwest Airlines located on Airport Blvd W in Sacramento recently tested positive for Covid-19.
Source: abc10.com ”
Southwest Airlines, 8835 Bear Road, ORLANDO, FL, 32826, USA
February 9, 2021 12:00 PM
“1. At the Orlando International Airport, in, or near the Southwest Airlines Cargo Warehouse and associated offices, the employer is not following the Centers for Disease Control and Prevention (CDC) guidelines to protect employees from exposure to SARS-CoV-2, the virus that causes COVID-19, in that employees are... allowed to be in Close Contact (see note below) with other employees who have COVID-19. 2. At the Orlando International Airport, in, or near the Southwest Airlines Cargo Warehouse and associated offices, the employer is not following the CDC guidelines to protect employees from exposure to SARS-CoV-2, the virus that causes COVID-19, in that employees who have had Close Contact (see note below) with other employees who have COVID-19, are not being quarantined. Note: Close Contact is defined by CDC as someone who was within 6 feet of an infected person for a cumulative total of 15 minutes or more over a 24-hour period starting from 2 days before illness onset (or, for asymptomatic patients, 2 days prior to test specimen collection) until the time the patient is isolated.
Source: Osha.gov | Receipt Date: 2021-01-15 ”
Southwest Airlines, 2378 Sunport Blvd, Albuquerque, NM, USA
September 9, 2020 12:00 PM
“An employee(1) at SOUTHWEST AIRLINES in ALBUQUERQUE, NM tested positive for Covid-19. Event Date: 09/09/2020
Source: env.nm.gov ”
An employee test positive for Covid-19, East By Southwest, 2905 Rodeo Park Drive East, Santa Fe, NM, USA
East By Southwest, 2905 Rodeo Park Drive East, Santa Fe, NM, USA
September 9, 2020 12:00 PM
“An employee(1) at HUB INTERNATIONAL SOUTHWEST in SANTA FE, NM tested positive for Covid-19. Event Date: 09/08/2020
Source: env.nm.gov ”
Covid-19 OSHA Complaint, Luis Muñoz Marín International Airport (SJU), Avenida Aeropuerto, Carolina, Puerto Rico
Luis Muñoz Marín International Airport (SJU), Avenida Aeropuerto, Carolina, Puerto Rico
July 29, 2020 12:00 PM
“1. They only give a glove. 2. No alcohol. 3. There is no security in the ramp area. 4. No masks or hand sanitizer
Source: Osha.gov | Receipt Date: 5/18/2020 ”
Recent Interesting Reports
Parque Bicentenario, Av. Río Amazonas, Quito, Ecuador
July 28, 2021 9:18 PM
“Despite the large number of people there were, everything was pretty fast and organized. I just had a little pain in my arm, where I got the vaccine for a day. ”
Pfizer Smoking cessation treatment - recalled due to N-Nitroso Varenicline content above ADI level, USA
July 19, 2021 3:02 PM
“Company name: Pfizer
Brand name: CHANTIX
Product recalled: Smoking cessation treatment
Reason of the recall: N-Nitroso Varenicline content above ADI level
FDA Recall date: July 19, 2021
Recall details: Pfizer is voluntarily recalling two lots of Chantix 0.5mg Tablets, two lots of Chantix 1 mg Tablets, and... eight lots of a Chantix kit of 0.5mg/1 mg Tablets to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-varenicline, above the Pfizer established Acceptable Daily Intake (ADI) level.
Long-term ingestion of N-nitroso-varenicline may be associated with a theoretical potential increased cancer risk in humans, but there is no immediate risk to patients taking this medication. The health benefits of stopping smoking outweigh the theoretical potential cancer risk from the nitrosamine impurity in varenicline. Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time.
Chantix is a treatment to help patients quit smoking and is intended for short term use. People who smoke cigarettes are 15 to 30 times more likely to get lung cancer than people who do not smoke. Smoking is also associated with many other cancers. CHANTIX has a safety profile that has been established over 15 years of marketing authorization and through a robust clinical program. Pfizer believes the benefit/risk profile of CHANTIX remains positive. Patients currently taking Chantix should consult with their doctor to confirm if they received an affected lot, and if appropriate, about alternative treatment options.
To date, Pfizer has not received any reports of adverse events that have been related to this recall.
The product lots were distributed nationwide to wholesalers and Distributors in the United States and Puerto Rico from June 2019 to June 2021.
For more recall details including the NDC, Lot Number, Expiration Date, and Configuration details for Chantix Tablets check: fda.gov
Source: FDA ”
July 11, 2021 3:25 PM
“I saw the chain saw advertised on Facebook and ordered it 4 months ago and still have not recieved it they got my money though. And can not get a real tracking number. ”
Billings, Montana, USA
July 13, 2021 4:17 PM
“I ordered the Battery-Powered Wood Cutter, this is the second one I’ve ordered and have not received I either want my money back for 2 or I want them sent. On April 15th they shipped a Battery Powered WOOD CUTERR, I have not received it yet, plus... I ordered one before this, I would like to know where they are, Aphitrite Technology limited ”
July 14, 2021 7:27 PM
“I have had this bait and switch happened to me twice, once by this company and once by another company. The little wires are used by campers to cut small branches. Both times. I paid through PayPal. I ordered the rechargeable battery mini saw pruner. I received... a wire. Contacted the seller and the seller offered me a 50% refund, I told the seller I wanted 100% of my money back. The seller then replied that he would request a 60% refund but he could not give back 100% unless I returned the product to China. It costs like 30 dollars to send to China from the US even though they claim they are US based. The seller said they had shipped product and paid logistic cost to ship it to me and would I please accept the 60% and he hoped I understood. These bait and switch practices are illegal in the US. I escalated the case to Paypal. Then waited for the review. I then received an email from PayPal stating the seller had provided a shipping number and they found in favor of the seller. This message is generated by an auto responder. I then called PayPal and requested to speak to a PayPal agent. With in 2 minutes the person could see the Seller had done this over and over. They refunded my money and apologized for the inconvenience the Seller had caused me. It takes some time and effort, but persistence pays off. Also, it I s not your responsibility to return the product they shipped back to them at your expense.
They are located in Tennesee the key is to start the case through Paypal, when Paypal finds in favor of the seller. Call PayPal and speak with an agent. The message you received is sent out by an auto responder. PayPal agents can see that it us a recurring issue and your money will be refund. If you paid by credit card contact thr company snd ask them to do a charge back. ”
July 6, 2021 2:14 PM
“On 5/11/21, ordered a wood cutter for final payment of 25.99.
I received some wire contraption instead. No answer to emails sent. Scam. Do not order any products from FaceBook unless you like throwing away your money. ”
July 14, 2021 9:01 PM
“Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
Product recalled: Sunscreen
Reason of the recall: Testing identified low levels of benzene
FDA Recall date: July 14, 2021
Recall details: Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen... product lines to the consumer level. Internal testing identified low levels of benzene in some samples of the products. Consumers should stop using the affected products and follow the instructions set forth below.
The only sunscreen products impacted are aerosol products, specifically: NEUTROGENA® Beach Defense® aerosol sunscreen:
- NEUTROGENA® Cool Dry Sport aerosol sunscreen
- NEUTROGENA® Invisible Daily™ defense aerosol sunscreen
- NEUTROGENA® Ultra Sheer® aerosol sunscreen
- AVEENO® Protect + Refresh aerosol sunscreen
Benzene is classified as a human carcinogen, a substance that could potentially cause cancer depending on the level and extent of exposure. Benzene is ubiquitous in the environment. Humans around the world have daily exposures indoors and outdoors from multiple sources. Benzene can be absorbed, to varying degrees, by inhalation, through the skin, and orally. Based on exposure modeling and the Environmental Protection Agency’s (EPA) framework, daily exposure to benzene in these aerosol sunscreen products at the levels detected in our testing would not be expected to cause adverse health consequences. Out of an abundance of caution, we are recalling all lots of these specific aerosol sunscreen products.
While benzene is not an ingredient in any of our sunscreen products, it was detected in some samples of the impacted aerosol sunscreen finished products. We are investigating the cause of this issue, which is limited to certain aerosol sunscreen products. Sunscreen use is critical to public health. Melanoma incidences continue to increase worldwide, and the majority of cases are caused by excessive sun exposure. It is important that people everywhere continue to take appropriate sun protection measures, including the continued use of alternative sunscreen.
The recalled sunscreen products are packaged in aerosol cans. The products were distributed nationwide through a variety of retail channels.
Consumers should stop using these specific products and appropriately discard them.
Check the full recall details on fda.gov
Source: FDA ”
Brookville, OH, USA
July 11, 2021 10:50 AM
“Yeah I never received this item I would like my money back, Ordered off of Facebook got from yeahyard a miniature saw pruner
Thank you ”
July 23, 2021 12:03 AM
“Company name: HIS
Brand name: HIS
Product recalled: Dietary Supplement for Weight Loss
Reason of the recall: Undeclared Sibutramine
FDA Recall date: July 22, 2021
Recall details: Palisades Park, NJ, HIS is voluntarily recalling all lots and all presentations of Miss Slim (10 count & 30 count... capsules) to the consumer level. HIS decided to recall Miss Slim after it was contacted by the FDA regarding the presence of sibutramine in the product.
Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues. The presence of sibutramine in Miss Slim renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. To date, HIS has not received any reports of adverse events related to this recall.
The product is marketed as a dietary supplement and is packaged 10 count UPC (742137605030) and 30 count UPC (609728434472) capsules. The product sold online at missslimusa.com.
Risk Statement: Products containing sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.
HIS is notifying its customers by website missslimusa.com and is arranging for return of all recalled products. Consumers that have Miss Slim which is being recalled should stop using it. 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.
Check the full recall details on fda.gov
Source: FDA ”
Purple Sage Lane, Hutto, TX, USA
July 19, 2021 6:51 PM
“Ordered hand chainsaw from them off Facebook. I got a weird metal string thing that I almost threw away because I nor anyone I asked knew what the hell it was. What a ripoff!!! I am trying to get my money back, but if they think for... one moment that I'm going to pay to have that piece of sh*t sent back to them, they better think again!! ”