McDonald's, 160 SW Marine Dr, Vancouver, BC V5X 2R1, Canada

3 individuals at Zach Core Knowledge Elementary School in Larimer county tested positive for Covid-19. The outbreak began on 10/18/2021

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April snow has left thousands in Oregon and Southwest Washington without power early Monday morning.'

Outage link: clarkpublicutilities.com
Source: koin.com
Published: 2022 04 11 See Less

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Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2021-10-21 See Less

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Within the last week, there has been an outbreak of staff members coming down with COVID-19. They have nurses that have been tested positive for COVID and they are still working. They are not providing N-95 masks. They have approximately 110 staff members that have been exposed... See More to COVID-19 and they are not providing testing for the employees.


Source: Osha.gov | Receipt Date: 2021-01-04 See Less

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Employees are using chemicals without proper training, multiple employees have tested positive for covid, employer is not disinfecting,


Source: Osha.gov | Receipt Date: 2021-05-10 See Less

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The Pot Zone doesn't have a scheduled cleaning time. They also haven't ever stocked disinfectant to clean high contact areas. Most of the employees don't take the mask mandate seriously and will constantly take their masks off, even in high traffic areas, while customers aren't present. I... See More have also witnessed each one of the leads allow customers without masks in simply because they didn't have one and the store hasn't stocked disposable masks for weeks. All of these together provide not only a health hazard to the employees, but to the community as a whole. POT ZONE 7701 Ne Hwy 99 Vancouver, WA 98665


Source: Osha.gov | Receipt Date: 2021-05-10 See Less

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Rusty pipes and what is believed to be black mold under the bar exposing all staff. Non-existent floor in the bar. They put down a piece of plywood for the bartenders to stand on that gets slippery when the floor floods everyday which caused a bartender to... See More slip and cut themselves, resulting in stitches. There is a hole in the floor in one of the server stations. They have a table top covering it. Someone fell through the floor because it was rotting and they just covered it and haven't bothered to fix it. They don't follow the CDC guidelines of if you're sick, stay home. They bully employees into working when they feel sick, resulting in mass COVID exposure. The general manager laid hands on an employee, she was walking and she grabbed her by her arms and spun her around and got in her personal space. The roof has been leaking for months. They have a knife on the top shelf in the bar that could result in serious injury or death. WHO SONG & LARRYS 111 E Columbia River Way Vancouver, WA 98661


Source: Osha.gov | Receipt Date: 2021-05-18 See Less

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At Killer Burger there is no Covid-19 policy, or Covid-19 training for employees. High touch areas such as the tablet and the time clock are not sanitized, and the restrooms are not cleaned. Social distancing measures are not taken seriously or enforced, such as the 6- barriers... See More at the register and the building occupancy. Pre shift health screening questions are not thorough, and sometimes skipped all together. An employee tested positive for Covid-19, and no actions were taken by the employer. No contact tracing, no deep cleaning, etc. Employees are not required to stay home or quarantine when symptomatic or exposed to possible Covid-19. Employees come to work sick. There have not been any safety meetings held since June of 2019, when meetings are required monthly at the minimum. Restaurant equipment such as gas, electric grills, and fryers are occasionally left on overnight and hot when the openers need to come in to clean them, or change out the contents. Leaving the building smelling strongly of gas in the mornings. The owner has not addressed any of the safety concerns when that happens with the closers. We have not had a fire drill in almost 2 years, and there has been no additional training to the staff as required by law. There are no accident reports on site, and leaders have not been shown how to report an accident, or how to deal with an injury onsite. There is not a no workplace violence policy. There is an employee that acts aggressive and throws things. There is no general safety policy or code of conduct posted, or otherwise disclosed for reference purposes. KILLER BURGER 616 Ne 81st St Ste F Vancouver, WA 98665-8136


Source: Osha.gov | Receipt Date: 2021-03-22 See Less

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1. An employee who tested positive for Covid-19 is being made to work after only 4 days of quarantine, while exposing approximately 7 coworkers, and customers who enter into the building. Cleaning is not being done properly. 2. Store Owner is requiring an employee who tested positive... See More for Covid-19 to work after only 14 days of quarantine. 3. Employee test positive for Covid-19, exposing 7 other employees. Owner is wanting the employee who tested positive for Covid-19 to work after only 14 days of quarantine, employee is still showing symptoms. SUBWAY SANDWICHES #6 6725 Ne 63rd St 108 Vancouver, WA 98661


Source: Osha.gov | Receipt Date: 2021-03-25 See Less

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Location of alleged hazard(s): Assembly, Shipping and Receiving areas 1400 NE 136th Ave. Vancouver, WA 98684 Description of alleged hazard(s): - A section of the company refuses to comply with the mask mandate - Over 9 of the 25-30 people in the area have contracted COVID-19 -... See More They are in close proximity to each other


Source: Osha.gov | Receipt Date: 2020-10-21 See Less

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Had a power surge this morning with a loud pop and what sounded like something was being pulled off of our house. It was our for three hours and came back on.. now it is off again. See Less

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Something is very wrong with the billing periods as well as the billing, my bill are always through the roof & when I’m paid up they’re always sending outstanding bills & when I call they always claim I’m behind & that isn’t true every month my bill... See More is over three hundred but my monthly usage is only one hundred so how is this even possible, I need some help here please investigate fairly & truthfully someone, I and the others who are like me thank you so much, no one is above the law & no one should be taken advantage of. See Less

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Pfizer is voluntarily recalling five (5) lots of Accupril (Quinapril HCl) tablets distributed by Pfizer to the patient (consumer/user) level due to the presence of a nitrosamine, Nnitroso-quinapril, observed in recent testing above the Acceptable Daily Intake (ADI) level.

Nitrosamines are common in water and foods, including... See More 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.i Accupril is indicated for the treatment of hypertension, to lower blood pressure. 

Accupril is also indicated in the management of heart failure as adjunctive therapy when added to conventional therapy including diuretics and/or digitalis. Accupril has a safety profile that has been established over 30 years. To date, Pfizer is not aware of reports of adverse events that have been assessed to be related to this recall. Pfizer believes the benefit/risk profile of the products remains positive based on currently available data. Although long-term ingestion of Nnitroso-quinapril may be associated with a potential increased cancer risk in humans, there is no immediate risk to patients taking this medication. Patients currently taking the products should consult with their doctor or health care provider about alternative treatment options for them.

The NDC, Lot Number, Expiration Date, and Configuration details for these products are indicated in the tables below and photos of the products can be found at the end of this press release. The product lots were distributed nationwide to wholesalers and distributors in the United States and Puerto Rico from December 2019 to April 2022. Accupril® (Quinapril HCl Tablets), 10 mgAccupril® (Quinapril HCl Tablets), 20 mgAccupril® (Quinapril HCl Tablets), 40 mg.

NDC: 0071-0530-23
Lot Number: DR9639
Expiration Date: 2023 MAR 31
Strength: 10 mg
Configuration/ Count: 1 x 90 count bottle

NDC: 0071-0532-23
Lot Number: DX8682
Expiration Date: 2023 MAR 31
Strength: 20 mg
Configuration/ Count: 1 x 90 count bottle

NDC: 0071-0532-23
Lot Number: DG1188
Expiration Date: 2022 MAY 31
Strength: 20 mg
Configuration/ Count: 1 x 90 count bottle

NDC: 0071-0535-23
Lot Number: DX6031
Expiration Date: 2023 MAR 31
Strength: 40 mg
Configuration/ Count: 1 x 90 count bottle

NDC: 0071-0535-23
Lot Number: CK6260
Expiration Date: 2022 MAY 31
Strength: 40 mg
Configuration/ Count: 1 x 90 count bottle

Pfizer places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Pfizer has notified direct consignees by letter to arrange for return of any recalled product.

Wholesalers and distributors with an existing inventory of the lots, listed in the table above, should stop use and distribution and quarantine the product immediately.

If you have further distributed the recalled product, please notify any accounts or additional locations which may have received the recalled product from you.

If you received free product through the Pfizer Patient Assistance Program (PAP) or the Pfizer Institutional Patient Assistance Program (IPAP), please check your stock immediately against the table above. If you have any of the affected product lots in your inventory, please follow the instructions above for returning the product to Sedgwick. Additionally, if you are aware of any patients to whom you dispensed the affected lots who still may have the product in their possession, please ask them to return the product to you.

Patients who are taking this product should consult with their healthcare provider or pharmacy to determine if they have the affected product.

Company name: Pfizer
Brand name: Pfizer
Product recalled: Accupril (Quinapril HCl) tablets 10mg, 20mg, 40 mg
Reason of the recall: Due to N-Nitroso-Quinapril Content
FDA Recall date: April 22, 2022

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Heartland farms about dog food I purchased. I bought the big bag of heartland farms dog food yesterday and tonight my dogs got sick and got diarrhea | Symptoms: Diarrhea See Less

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I order an Africa fabric from amazon. it was sent to the USPS Avenel NJ location via SF Express. my package was scanned in that facility at 9.05am on 4/11/2022 until now 4/29/2022 my package is seating in that facility. I have no information. Why is my package not being delivered? See Less

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My dog has been having seizures for 2 year's w no known cause after many tests & trips to the emergency vet. He started throwing up the peanut butter dream bones, I finally found the source of his seizures & him being not well. I am outraged... See More that these so called treats would be on the market! After all my family is going through. After reading how many families have lost their fur babies from these poisonous, dangerous "treat"!! There is no amount of money that could give my family our time back w the worst experience for the past 2 years!!! It's literally killing him! What's wrong w you people???.!!!! See Less

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Babyganics is voluntarily recalling two lots of 20-ounce bottles of babyganics® 20oz chamomile verbena bubble bath, due to the presence of the bacterium Pluralibacter gergoviae. The products were sold in the last two months only at select retailers in the U.S.

During internal testing related to product... See More shelf life across the Babyganics bubble bath line, it was discovered that two specific lot numbers of this product contained the bacterium. While infants may be more susceptible than adults, Pluralibacter gergoviae does not usually cause healthy individuals to become sick. However, it may pose a risk of infection to those who are immunocompromised or have broken or irritated skin, such as diaper rash.

The only products affected are babyganics® 20oz chamomile verbena bubble bath UPC 8 13277 01375 4 with lot codes Y314 and Y315 found at the bottom of the packaging and contained in a white plastic bottle with a green plastic lid.

The testing confirmed that no other Babyganics products contained this bacterium. Babyganics takes pride in its commitment to vigorous consumer safety standards and providing peace of mind for parents, which is why the decision was made to voluntarily recover these bottles from retailers and to proactively reach out to consumers. Consumers with the affected product will be provided with a full refund after submitting their product and contact information at the company website. Consumers who have come into contact with the affected product and aren’t feeling well should contact their doctor.

Company name: Babyganics
Brand name: Babyganics
Product recalled: Chamomile verbena bubble bath
Reason of the recall: Presence of the bacterium Pluralibacter gergoviae, a bacterium
FDA Recall date: April 20, 2022

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I have had two packages that have 'gone missing' with USPS and have now had to refund customers. The packages never seem to leave NJ and both contained the same single items (a CD). The first small media mail package was sent on March 15th, 2022 -->... See More Departed post office in Pitman, NJ on Mar 15 --> arrived at South Jersey NJ Distribution Center March 15 @ 3:54pm --> March 19th - In transit to next facility and no updates after that. During April: spent a few calls completing the 'missing mail' forms both electronically and speaking to 'investigators' who promise to call back. When I receive call-backs it's to say that my missing mail electronic form 'wasn't fully filled out' or that 'the missing report action has not been updated' or that they are 'now pushing it forward.' No notifications from the USPS since then. My second package that I am going to have to refund the customer for was another small media mail package with CD sent April 25th 2022 --> USPS in possession from Sewell NJ --> April 25 2022 Departed Post Office Sewell NJ --> April 29 2022 "In transit, arriving late". It is now May 17th and still no package to the customer. See Less

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Alpine Fresh, Inc. of Doral, Florida is voluntarily recalling its 1 pound packages of "Hippie Organics" French Beans from lot# 313-626, because they have the potential to be contaminated with Listeria monocytogenes. The recalled "Hippie Organics 1lbs French Beans" were distributed in Whole Foods (CT, FL, GA,... See More IL, MD) , Aldi (FL) and LIDL (DE, GA, MD, NJ, NY, NC, PA, SC, VA) retail stores.

Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The product comes in a 1 pound, clear plastic package marked with lot # 313-626 on the back on a small, white label. No illnesses have been reported to date in connection with this problem. The potential for contamination was noted after routine testing by the company revealed the presence of Listeria monocytogenes in 1 pound packages of "Hippie Organics French Beans  From lot # 313-626." The problem has been found to be isolated to the identified lot and the company has taken corrective actions to prevent a recurrence. Consumers who have purchased 1 pound packages of "Hippie Organics French Beans from lot #313-626" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-866-827-3362.

Company name: Alpine Fresh, Inc.
Brand name: Hippie Organics
Product recalled: French Beans
Reason of the recall: Listeria monocytogenes contamination
FDA Recall date: April 21, 2022

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Natural Organics, Inc., is voluntarily recalling four lots of NaturesPlus Keto Living Sugar Control Capsules 90 count, because it was found to contain gluten. People who have allergies to wheat or gluten run the risk of serious or life-threatening allergic reactions if they consume these products. There... See More have been no reported incidents of illness or adverse reactions in connection with these products to date.

Individuals with Gluten intolerance may experience minor to severe reactions after consuming this product. This could include upset stomach, diarrhea, fatigue, skin reactions and more. It was discovered during routine testing that the product contains gluten. It was subsequently discovered that a raw material that is normally gluten free tested positive for gluten.

Gluten is a general name for the proteins found in wheat (wheatberries, durum, emmer, semolina, spelt, farina, farro, graham, KAMUT® khorasan wheat and einkorn), rye, barley, and triticale – a cross between wheat and rye.

The listed products were distributed nationwide to consumers, retail stores and to the following foreign countries: Kenya, Spain, Trinidad, United Arab Emirates, and the United Kingdom. The capsules are packaged in white jars and black caps; with labels having orange, white and black print bearing the product codes, lot numbers and “Best By” or “BBE” (Best Before End) dates are printed on the bottom of the bottle.

The lots affected are:

- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. 82004, UPC Code 097467820043, Lots 1362073, Best By 10/2025 and 1365200, Best By 10/2025
- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. Ue82004, UPC Code 097467820043, Lots 1361754, BBE 10/2025 and 1364325, BBE 10/2025

Consumers who may have purchased affected lots of NaturesPlus Keto Living Sugar Control Capsules are advised to return them to the place of purchase. No other Natural Organics, Inc. products are affected by this recall. Natural Organics, Inc. has removed all affected products within existing inventory.

This voluntary recall is announced in accord with FDA guidelines. We are initiating recall notices to our accounts and consumers who received inventory of the recalled products with instructions for returning the recalled products and for notifying their customers of the recall. Consumers with questions may contact the company Monday – Friday, from 8:00 am to 4:30pm EDT.

Company name: NATURAL ORGANICS, INC
Brand name: NaturesPlus
Product recalled: Keto Living Sugar Control Capsules
Reason of the recall: Undeclared Gluten
FDA Recall date: May 06, 2022

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