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McDonald's, 31 Providence Hwy, Norwood, MA 02062, United States
Covid-19 OSHA Complaint, Intarome Fragrance & Flavors, Corp., 370 Chestnut Street, NORWOOD, NJ, 07648, USA
3 weeks ago
1. Employee are getting sick with Covid and the company is not doing anything to protect employees. 2. Company is not complain with CDC guidelines regarding social distancing, or disinfect the areas 3. Company does not informed employees about other employees being sick from covid 19. 4.... There are holes on the floor and is very hard to operate the forklifts 5. Improper flammable storage. 6. Emergency exits are blocked by merchandise.
Alleged Hazards: 6, Employees Exposed: 57
Source: Osha.gov | Receipt Date: 2021-02-10
Covid-19 OSHA Complaint, Dan O'Brien Kia Norwood, 105 Boston Providence Highway, NORWOOD, MA, 02062, USA
4 months ago
1. Employees have been exposed to positive Coid-19 employees and were not informed in accordance with OSHA, CDC and State guidance. 2. Employees who were exposed to co-workers who tested positive were not isolated and/or quarantine; instead they were allowed to work potentially exposing their co-workers. 3.... When an employee has tested positive for Covid-19 and daily the employer is not performing adequate cleaning and disinfecting of the premises in accordance with OSHA, CDC and State guidelines. 4. The employer does not have a COVID Policy and procedures.
Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-04-21
5 months ago
6 individuals at Norwood Public School in San Miguel county tested positive for Covid-19. The outbreak began on 27-05-2021
Covid-19 OSHA Complaint, The Buckingham at Norwood Care and Rehabilitation Center LLC, 100 McClellan St., NORWOOD, NJ, 07648, USA
6 months ago
There are COVID-19 positive patients or patients with symptoms in the facility, however proper protocols have not been followed. Adequate sanitation tools have not been provided. Adequate training has not been provided to the staff.
Alleged Hazards: 3, Employees Exposed: 8
Source: Osha.gov | Receipt Date: 2020-03-27
1. Crowds within the employee work area is resulting in drivers and pre-loaders being incapable of keeping at least six foot distance. 2. Trucks are parked close together making it difficult to social distance. 3. Management is not setting up warehouse and power belt so that trucks... are kept at a distance to ensure employees are not working next to each other. 4. Management is allowing numerous employees to work and walk along the power belt to grab packages, increasing risk of COVID-19 spread in the work place.
Alleged Hazards: 4, Employees Exposed: 200
Source: Osha.gov | Receipt Date: 2021-03-10
8 months ago
1) There are no paper towels in the facility's restrooms; 2) Mask use inside the facility is not enforced to reduce employee transmission of COVID-19
Alleged Hazards: 2, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2020-12-09
9 months ago
Norwood Facility 1) A truck was not sanitized after a driver became ill, was replaced, and subsequently tested positive for Covid-19 2) Employees in contact with employees who test positive for Covid-19 are not being informed of the potential exposure 3) The site safety team has been... reduced which has hindered access to PPE and Cleaning Supplies 4) Employees working around the belt are not social distancing
Alleged Hazards: 4, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-12-29
9 months ago
1) The employer is holding large meetings indoors with up to 35 workers, increasing risk of exposing employees to COVID-19; 2) The employer is not making sure employees maintain at least 6 foot distance in all direction from co-workers during indoor meetings.
Alleged Hazards: 2, Employees Exposed:... 100
Source: Osha.gov | Receipt Date: 2021-01-05
1045 Univeristy Avenue, Norwood, Ma 1) Workers are not wearing masks when working inside or when outside. New employees and managers do not wear face masks. 2) Workers are not social distancing when unloading trucks or sorting. 3) The employer does not inform employees when other workers... in their area have gotten coviid-19. The employer does not tell workers who have worked with employees who got covid-19 to get tested and to quarantine. 4) Nobody wears masks in the cafeteria. 5) The building is not sanitzied after workers test positive. 6) There are no handwipes. 7) There are no paper towels in the bathroom.
Alleged Hazards: 8, Employees Exposed: 300
Source: Osha.gov | Receipt Date: 2020-12-18
1045 University Avenue, Norwood, Ma. Employees who work together in close quarters such as a delivery van are not instructed to get tested and to quarantine when one of the employees has covid symptoms.
Alleged Hazards: 1, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2020-12-21
Recent Interesting Reports
Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... no illnesses reported to date.
During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.
The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.
The full list of affected products is on the link below.
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. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.
Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements
Check the full recall details on the FDA website: fda.gov
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
The Procter & Gamble Company (NYSE: PG) is voluntarily recalling all lots with expiry through September 2023 of specific Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products sold in the United States, and listed in the table below, to the... consumer level due to the presence of benzene detected.
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. Based on exposure modeling and the cancer risk assessments published by the Environmental Protection Agency (EPA) (IRIS database), daily exposure to benzene in the recalled products at the levels detected in our testing would not be expected to cause adverse health consequences. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. To date, The Procter & Gamble Company has not received any reports of adverse events related to this recall and is conducting this recall out of an abundance of caution.
The affected products are used as antiperspirants and hygiene products and are packaged in aerosol cans. See the link below for Product names and UPC codes and images for further descriptions. They are recalling all lots with expiry through September 2023 of the products listed in the link below.
Company name: The Proctor & Gamble Company
Brand name: Old Spice Secret
Product recalled: Old Spice and Secret Aerosol Sprays
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 23, 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.
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
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
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