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Menifee, California, United States
Updated: November 25, 2021 5:53 PM
1 day ago
Power has been shut off as part of public safety power shutoffs in certain areas of Menifee to reduce wildfire ignition.
Source publication date: 2021 11 25
Covid-19 OSHA Complaint, Dave Williams Plumbing and Electrical, Inc, 29914 Antelope Rd, Menifee, CA, USA
4 months ago
1. T8CCR 3205(c)(7)(A Employer not ensuring face coverings are worn by employees over the nose and mouth. 2. T8CCR 3205(c)(8)(D) Employer not providing employees with an effective hand sanitizer. 3. T8CCR 3364(b) Employer not keeping toilet facilities clean.
Alleged Hazards: 3, Employees Exposed: 13
Source: Osha.gov |... Receipt Date: 2021-02-17
Covid-19 OSHA Complaint, Consolidated Contracting Services, Inc, 29914 Antelope Road, Menifee, CA 92584, USA
5 months ago
T8CCR 3203(a) Not following Covid-19 protocols. Not requiring face coverings. Social Distancing not enforced. Not enough sanitizing stations. Throughout jobsite
Alleged Hazards: 4, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-11-19
T8CCR 3205(c)(11) T8CCR 3205(c)(2)(C) Employer not quarantining employees who have been exposed to other employees that have tested positive to Covid-19. Employer not following quarantine time for employees who tested positive to Covid-19.
Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2021-01-26
Recent Interesting Reports
Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products.
Risk Statement: Benzene is... classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.
To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See the link below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically the ones listed in the link below.
The products were distributed nationwide in the United States through various retailers. Consumers, distributors, and retailers that have product which is being recalled should stop using or selling these specific Odor-Eaters® spray products and dispose of them appropriately.
Company name: Odor-Eaters®, owned by Blistex Inc.
Brand name: Odor-Eaters®
Product recalled: Oder Eaters spray products
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 17, 2021
Check the full recall details on fda.gov
NJ post office is a ‘black hole’, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
3 weeks ago
On 9-24-21 I valued package was returned using Pitney Bowes shipping label provided by the merchant (American Mint). It was dropped off at the USPS store in Daytona Beach, picked up by Daytona Beach Post Office on 9-28-21 and retrieved from that Post office by Newgistics (Pitney... Bowes) on 9-30-21. On 10-4-21 it arrived and was dispatched from sorting at the Monroe Township, Middlesex County, New Jersey Post Office. Since then it is missing, in a black hole, unable to be found. This is a shame since this is a product scammed to my mother (senior of 86) who followed every step to have her $149.99 from American Mint and now can not receive her money back since the company has not received the product back. Please address this issue to return what is rightfully my mother's. This is a shame.
Pitney Bowes Returns
Parcel Return Service 56901
Tracking # 4205690192023901007848000000499942
MaryRuth’s, a leading omni-channel health and wellness brand that offers vitamins, minerals, and supplements for the entire family, today announced that, out of an abundance of caution, it is voluntarily recalling two lots of its liquid probiotic for infants (1oz) due to the possibility of contamination by... Pseudomonas aeruginosa.
Pseudomonas aeruginosa is a microorganism found in the environment that, if ingested, can cause infection in immunocompromised individuals or, rarely, in very young infants. P. aeruginosa infections in immunocompromised infants are generally limited to hospital settings. In such settings, there is the chance that the infant’s immature gut will not be able to prevent P. aeruginosa from gaining access to the blood, and from there it can disseminate elsewhere in the body, resulting in the possibility of serious adverse health consequences.
This recall only affects two lots of the product, Lot #100420218 and Lot #100520218, UPC barcode number 856645008587. Lot numbers are located on the side of the bottle and on the bottom of the outer container in which the product is sold. No other lots or any other MaryRuth’s products are affected by this recall. This product is distributed nationwide through Target, Amazon, and direct sales from the company’s website.
The company is asking consumers to throw away product from both affected lot numbers. The company discovered the potential issue with one of its manufacturing partners during routine laboratory testing.
The only product complaint the company has received with respect to the affected product lots was one report of temporary diarrhea in an older infant after consuming the product, which the company does not believe was related to the presence of the microorganism.
Company name: MaryRuth’s
Brand name: MaryRuth’s
Product recalled: liquid probiotic for infants
Reason of the recall: Potential contamination with Pseudomonas aeruginosa
FDA Recall date: October 29, 2021
Check the full recall details on fda.gov
1 week ago
Package was supposed to be delivered November 6, 2021.
After days of endless calls finally told it left teterboro post office November 5 but was never delivered or tracked since.
Nag Champa Incense Caused Abnormal Allergic Reaction In Dog With This Particular Package of It, Archimage, Monroe Avenue, Rochester, NY, USA
2 weeks ago
Usually is fine. Not this time. I decided to burn Nag Champa incense to meditate. As I was meditating, our dog started sniffling and then began throwing up large amounts of mucous. Her lips were swollen and pulled back slightly. She is ok now, but I've never... experienced anything like this using incense before this happened. I often use it for meditation. I called the vet who confirmed this is an allergic reaction and they informed me to monitor her and ensure she is safeand healthy, not vomiting anymore. They instructed me to open all the windows and doors, turn on ceiling fans,and run the furnace heat to pull remaining particulate into the HEPA filter on the furnace and then to replace the filter tomorrow to ensure it doesn't just recirculate the particulate if any happens to get through. Also said to wash hard surfaces in the room it was burned on and vacuum up any furniture,carpet, or rugs there to remove any settled particulate. I'm not sure what went wrong here. I've never had this happen with her or any other dog when burning this.
But even I am sniffling and nauseous after having burned it and my throat is sore. I took benedryl to
prevent an attack in me personally.
Nag Champa incense sticks.
Label information: Nag Champa Agarbatti Satya Sai Baba. Mfrs. Shrinivas
Sugandhalaya(BNG)LLP.1/9,8th Cross, Magadi Road, Bengaluru-560023, India. Certified green
product. Export Quality.2021 Series. Hand Rolled in India. UPC 8904245400491.Warning: insist for this label to avoid imitation buy from reputed dealers only. Earth. Contains seals with hologram over each side of the box with official logo. NetWt.40g. Quality assurance labels are not actual stickers demonstrating actual checks, but are instead printed onto the package to appear as if they were actual quality assurance stickers and are offset with a white background to trick a consumer. There are three which areas follows. Fake QA sticker1: Quality Assurance Management ISO 9001(check mark symbol)
Fake QA sticker2: Environmental Management ISO 14001(check mark symbol) Fake QA sticker 3: Occupational Health &
Safety OHSAS 45001 (check mark symbol).
Customer care number+917022000111
Item purchased at Archimage. Not their fault. They only buy reputable authentic items and this has to be a bad or contaminated batch here. | Symptoms: Nausea, Other
Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared wheat, milk, soy and/or coconut on the labels. People who have an allergy or severe sensitivity to soy, milk, wheat, or coconut run the risk of serious or life-threatening allergic reaction if... they consume products containing soy, milk, wheat, or coconut.
On 11/4/2021 during an FDA inspection the firm was notified that their labels failed to disclose the presence of allergens on some of their products. The recalled products were shipped between June 4, 2020 through October 1, 2021 to distributors and retailers in Alabama, California, Florida, and Texas. There have been no illnesses reported to date.
The affected products are:
Brand: Boba Origin. Product: 100% Whey Protein Isolate. Flavor: Brown Sugar Milk, Tea, Undeclared milk, & soy. Size: 1 gallon plastic jar. Lot No. 2106263. Exp. 07/2023
Brand: Etedream. Product: Etegrow ISO. Flavor: Snicker Doodle, Undeclared milk. Size: 2gallon plastic jar. Lot No. 2106002. Exp. 06/2023
Brand: RAW. Product: Vegan Protein Flavor: Peanut Butter, Undeclared coconut. Size: 1gallon plastic jar. Lot No. 2108070, 2104340, 2102018, 2012304, 2010266, 2010102, 2007037/746, 2005132. Exp. 08/2023, 04/2023, 02/2023, 12/2022, 10/2022, 10/2022, 07/2022, 05/2022
Brand: Steel. Product: Veg-Pro Flavor: Cookies & Crème, Undeclared Wheat. Size: 64 ounce plastic jar. Lot No. 2109390, 2104333, 2011260, 2104007/1041, 2105059, 2011260/994. Exp. 09/2023, 04/2023, 11/2022, 04/2023, 05/2023, 11/2022
Brand: Vital Force. Product: PureISO. Flavor: Milk Chocolate, Cocoa, Undeclared milk. Size: 1gallon plastic jar. Lot. No. 2108191. Exp. 09/2023
Brand: Vital Force. Product: PureISO. Flavor: Creamy Peanut, Butter Vanilla, Undeclared milk. Size: 1gallon plastic jar. Lot No. 2109068. Exp. 09/2023
Lot numbers and expiration dates are found on the bottom of each container.
Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall.
This recall is being made with the knowledge of the Food and Drug Administration.
Company name: Nutracap Holdings, LLC
Brand name: Etedream, Vital Force, Raw, Boba Origin, Steel
Product recalled: Dietary Supplement Protein Powder
Reason of the recall: Undeclared wheat, milk, soy and/or coconut
FDA Recall date: November 09, 2021
Check the full recall details on fda.gov
I am a 42-year-old biologist. I had very good health overall before the injection. I did suffer from seasonal allergies, but otherwise enjoyed a full and active life. I took the first Moderna injection on March 17, 2021. I took the injection because I believed it was... needed to protect myself, my family, and others in my community. I believed the FDA, CDC, and doctors that it was safe, effective, and the right thing to do. I was told that the potential side effects were possible arm pain, headache, and flu like symptoms. The CDC backed up these claims on their website by listing the side effects as minor. I took the first injection on March 17, 2021, at 9:00 a.m. at the pharmacy. A rash appeared on my arm and torso within a couple of hours. Some veins in my arms popped. There was pain on my left arm, like I had been punched. I took Allegra and slept all day from the fatigue. It only got worse from there. My doctors ignored reactions from the injection and unbelievably recommended a second shot! They said it was needed to be safe. I took the second Modern injection on June 17, 2021. After the second injection, I got dizzy right away. I stayed at the pharmacy for thirty minutes because I thought I might faint. I was fearful before the second shot. Enough that I took an EpiPen (although expired) with me as a precaution after the last reaction. Two days after the second injection, I could not even get out of bed. As the day progressed, I couldn’t perform my work on the computer. My eyesight became so blurred that I couldn’t read my email. I was dizzy when I got up. I had no choice but to stay down. That lasted at least two weeks. I still deal daily with fatigue, dizziness, memory problems, nerve pains, joint pains, burning of skin, numb ringing ears, headaches, and tingling sensations in my body. My face droops. My right hand tremors. Everyone involved in the coercion of this injection has badly harmed my daily life, my family, my work, and my health. They have taken ME away. They have taken me away from everything that made my life happy and fulfilling. Before the injection, I lived a normal, active and happy life. I worked full time, took care of my family, rescued dogs, and enjoyed a variety of physical activities. Now, I have an unnamed mysterious disorder which the doctors have told me they suspect is a variation of Guillain Bare. I suddenly have gastro issues and tachycardia. My headaches go back and forth between vestibular migraines and hemiplegic migraines. Those insane migraines take me out for hours, and sometimes days. The extreme inflammation on my brain from cytokine storm affects how I think, walk, and talk. I am unable to do the most basic tasks. Driving is completely out of the question! I cannot even drive myself anywhere, which has rendered me completely dependent on others. The effects of these shots are so extreme and never-ending. So far, no effective treatments have been found to help me. I have seen numerous specialists. I have tried special diets. I have undergone blood tests, PCP visits, neurological visits, ENT visits, cardiologist visits, immunologist visits, and many more. I have found no answers or guidance. There is no trajectory of improvement. No one knows if I will ever get better. This makes me feel really helpless and hopeless sometimes. As soon as I mention that symptoms are “vaccine” related, I feel completely ignored. No doctors want to talk about the possibility of vaccine injury. It took me six months to prove to my family doctor that I have been reacting to the “vaccine”. I spent countless hours, between the migraines and fatigue, researching desperately on my own. I even went over my medical records over the years to understand what is going on with my body. Being ignored by the medical community as well as friends and family that did not have an adverse reaction to the injection has taken a mental toll on me. At least those that live with me know the day-to-day issues and have never doubted the source. Side effects need to be acknowledged more publicly. More research needs to be done before we can push this into our kids or make mandates. Long term data is imperative and the only conscionable thing to do. | Symptoms: Other, Headache, Dizziness, Fatigue, Gas, Joint Pain
#moderna #modernacovid19vaccine #covid19vaccine #vaccine #youngsville #louisiana #unitedstates #headache #dizziness #fatigue #gas #jointpain
1 week ago
DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.
I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so... far today and STILL pieces of DreamBone Twist Sticks