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Pfizer Vaccine Phx Az (1st dose), Phoenix, AZ, USA
February 16, 2021 6:09 PM
Phoenix, Arizona, United States
Received first Pfizer injection Feb 10 2021. No reaction other than a bit of a sore arm...the same as when you would have a yearly flu shot.
March 8, 2021 11:00 AM
“Have had both doses of Pfizer. Only side effect was mild soreness at injection site. ”
February 13, 2021 12:12 AM
“Complete power failure while driving on the freeway. Jeep Cherokee 2019. Power turned completely off while driving on the freeway. Put it in park and was able to restart after coasting off the side of the freeway during rush hour and a baby in the backseat. Then it happened again while on a side str... eet a few minutes later. THIS IS DANGEROUS AND NO RECALLS!!!! This appears to be happening to a lot of people who have filed complaints against Jeep with 2019 Cherokees. Someone is going to die. This is so scary. My car is in excellent condition and with barely 20k miles. THIS NEEDS TO BE INVESTIGATED!!! ”
Covid-19 OSHA Complaint, U.S. Citizenship and Immigration Services (USCIS), 1330 S. 16th Street, PHOENIX, AZ, 85034, USA
February 10, 2021 12:00 PM
“The office usually has over 200 people come in daily but employees are not allowed to clean up after each applicant or family that they see. The office hardly ever has any sanitizing products to clean with, the workers are not given breaks. An employee has been hospitalized due to COVID and is on a... ventilator and contact tracing is not being done.
Alleged Hazards: 4, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-01-14 ”
An Employee test positive for Covid-19, Grand Avenue Pizza Company, 1031 Grand Ave, Phoenix, AZ 85007, United States
February 7, 2021 12:00 PM
“An employee at Grand Avenue Pizza Company located on Grand Ave in Phoenix recently tested positive for Covid-19.
Source: twitter.com ”
February 3, 2021 12:00 PM
“Item 1: The employer is having people with active COVID-19 report to work. Not following CDC guidelines, thus exposing multiple employees to COVID-19
Source: Osha.gov | Receipt Date: 2020-07-16 ”
February 3, 2021 12:00 PM
“Item 1: The General Manager does not wear a mask while working. He exposes employees that are in close contact with him when they talk. Item 2: The Finance employees do not wear a mask while working with customers present. Item 3: There are two Sales Managers that do not wear a mask while they work... with employees. Item 4: The company holds several meeting throughout the day with staff and do not require them to social distance. Item 5: The employer does not routinely wipe down commonly touched surfaces with a disinfectant to prevent the spread of COVID-19 in the workplace.
Source: Osha.gov | Receipt Date: 2020-12-01 ”
Covid-19 OSHA Complaint, Triwest Healthcare Alliance Corp., 15810 N 28th Ave, PHOENIX, AZ, 85053, USA
February 3, 2021 12:00 PM
“Item 1) The employer does not have a COVID-19 Response Plan to prevent the spread in the workplace. Item 2) A supervisor returned from a trip and displayed signs and symptoms of COVID and was not sent home for quarantine as per CDC guidelines.
Alleged Hazards: 2, Employees Exposed: 2
Source: Osha... .gov | Receipt Date: 2020-12-11 ”
January 25, 2021 6:15 PM
“Had vaccine on sat morning...felt fine until about 6:00 when i developed a a fever, bad body aches, chills, sweats, headache
felt awful the whole next day and feel a little better today but still not so good...hopefully tomorrow will be better ”
January 14, 2021 12:00 PM
“Item 1: The employer has not provided any employees with personal protective equipment (PPE) to prevent the spread of COVID-19 in the workplace. Item 2: The owner of the company refuses to wear a mask and places the rest of the employees at risk for COVID-19. Item 3: The office is not routinely clea... ned with sanitizer or disinfectant to prevent the spread of COVID-19. Item 4: The employer does not require staff or outside visitors to maintain a 6 foot distance while at work.
Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-05 ”
February 24, 2021 12:00 PM
“Item 1: No COVID Exposure Control Plan Item 2: COVID procedures not followed or enforced Item 3: Poor Housekeeping and sanitation Item 4: Employees exposed to contaminated sheets and towels.
Source: Osha.gov | Receipt Date: 2020-10-15 ”
Recent Interesting Reports
February 28, 2021 7:22 AM
“Ordered a mini chainsaw from Wayfale! What I got is a necklace! Am Stink Sour 😡!! I just have a little widow's pension, and for me it's a lot of money. The advertisement is so misleading!!! ”
February 10, 2021 10:00 PM
“Company name: NDAL MFG INC
Brand name: ManukaGuard
Product recalled: Allercleanse Nasal Spray
Reason of the recall: Due to Yeast Contamination
FDA Recall date: February 10, 2021
Recall details: NDAL MFG INC is voluntarily recalling one lot of Manukaguard Allercleanse, nasal spray to the consume... r level. The Allercleanse nasal sprays have been found to be contaminated with yeast.
Risk Statement: The use of Allercleanse (manuka honey) nasal spray contaminated with yeasts, in the population most likely to use it (children, adults, and elderly), may result in adverse events that necessitate medical or surgical intervention. However, use of this contaminated product in immunosuppressed individuals may result in life threatening invasive fungal infections.
NDAL MFG INC has not received any reports of adverse events related to this recall. The product is used as a NASAL SPRAY to clean nasal passages and sinuses of irritants and other environmental contaminants and is packaged in cardboard box with one nasal spray per box UPC 858631002128. The affected Allercleanse lot is lot # 2010045 and BB 10/2023 expiration date.
Product was distributed Nationwide in the USA to 1 e-commerce website amazon.com, distributors and retail stores. NDAL MFG INC has notified its distributors and customers by e-mail followed by telephone and further email and has arranged for return/replacement etc. of all recalled products.
Consumers/distributors/retailers that have product which is being recalled should stop using/return to place of purchase/discard/contact their doctor, etc., if they have not already done so. Consumers with questions regarding this recall can contact NDAL MFG INC by phone 1-800-916-1220 or e-mail address SUPPORT@MANUKAGUARD.COM, M-F 7:30 am to 4 pm PST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Check the full recall details on fda.gov
Source: FDA ”
February 11, 2021 11:05 AM
“Dont order any thing from black cass or funny 456 both r scams i order two saws and got two chains thats it i order a fold up scooter from funny456 and got a charger to what i do not know both arw full of crap and iam out money ”
February 15, 2021 4:47 PM
“The cashier is felling sick. Every one got flu in this restaurant. This place infected with COVID 19
I got full sick. All employees are sick and needed fully attention ”
February 21, 2021 7:00 PM
“I ordered a battery operated mini chainsaw. They sent me a chain with a strap on each end. After many emails they told me that I did order it. No, I didn’t. 5 shoulders, I wouldn’t have. I looked them up and that is when I started finding the reports. ”
March 3, 2021 8:00 PM
“Company name: Ridley Block Operations
Brand name: Ridley Block Operations
Product recalled: CRYSTALYX Sheep-lyx
Reason of the recall: Elevated levels of copper
FDA Recall date: March 03, 2021
Recall details: Ridley Block Operations is voluntarily recalling three batches of CRYSTALYX Sheep-lyx.... The product batches have been found to have elevated levels of copper, which is out of specification. With prolonged consumption, the affected product could potentially have adverse health effects on sheep. This recall relates only to CRYSTALYX Sheep-lyx with the following batch/lot numbers printed on the package:
- CRYSTALYX® Sheep-lyx™. B01769272. Item No./Product No: 7248. Package Info: 125# Block
- CRYSTALYX® Sheep-lyx™. B01769338. Item No./Product No: 7248. Package Info: 125# Block
- CRYSTALYX® Sheep-lyx™. B01769344. Item No./Product No: 7248. Package Info: 60# Block
No other batch/lot numbers or other Ridley Block Operations products are involved in this voluntary recall. Only the specific batches and lot numbers of CRYSTALYX Sheep-lyx listed above are impacted. No injuries or illnesses have been reported.
Ridley Block Operations has notified its customers of this voluntary recall. Products matching these batch/lot numbers should be removed from distribution/inventory and discontinued from feeding. Customers are encouraged to call Ridley Block Operations customer service at 1-903-480-0021 (Monday – Friday, 8:00 a.m. - 4:00 p.m. CT) for instructions on what to do with affected product inventory.
Check the full recall details on fda.gov
Source: FDA ”
March 6, 2021 11:31 AM
“The Ad was miss leading for a saw and received a chain. The Ad only had a picture of the Saw with description of chain. So you think you are getting a Saw with the chain. All I got was the chain. During shipping you get an email said one of your item is sent than you think 2nd item is on the way. I... contacted them for refund immediately. They won't refund me. They offered me 4%. Yep than 5%. They offered me a discount around 5% to buy their Saw over $85 only. I called their 800# but was a medical company. They refused my full refund $37.98 and offered about 4% than 5% is $1.49. Scam ”
February 21, 2021 9:27 AM
“I received the 2nd covid 19 vaccine shot from Pfizer at the Amazon site February 20th at 1:00 p.m..
I have a mildly sore right shoulder and no other symptoms. ”
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... on 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 ”
February 13, 2021 3:46 PM
“I bit and bought a $30 GT A26 saw and found out after I had ordered it, that it was only a chain. I contacted the company and said I wanted to upgrade to the $60 chainsaw that was on their website and they said no problem & I would get the whole thing. I just received it and it is a completely diff... erent chainsaw and now the saw is not on their website anymore. Wondering how I can get my money back. ”