Additional 5 employees confirmed positive for Covid-19, Planasa Oregon Operations, 8383 Short Rd, Klamath Falls, OR 97603, USA

November 26, 2020 12:00 PM

8383 Short Road, Klamath Falls, 97603 Oregon, United States

Additional 5 employees confirmed positive for Covid-19 at Planasa Oregon Operations, LLC in Klamath County. Investigation Start Date: 10/1/2020 , with the most recent onset of: 11/16/2020 New Cases of: 5

Source: www.oregon.gov

January 21, 2021 12:00 PM

“An employee at The Guenther House located on E Guenther St in San Antonio recently tested positive for Covid-19

Source: mysanantonio.com See Less”

January 21, 2021 12:00 PM

“An employee at LCBO located on Weston Road in North York recently tested positive for Covid-19

Source: lcbo.com See Less”

January 21, 2021 12:00 PM

“3 employees at Marine Atlantic North Sydney Terminal located on Prince Street in North Sydney recently tested positive for Covid-19

Source: saltwire.com See Less”

January 21, 2021 12:00 PM

“An employee at McDonald's located on Hays Boulevard in Oakville recently tested positive for Covid-19

Source: insidehalton.com See Less”

January 21, 2021 12:00 PM

“An employee at Supreme located on Bowery in New York recently tested positive for Covid-19

Source: twitter.com See Less”

January 21, 2021 12:00 PM

“An employee at Stoneface Brewing Company located on Shattuck Way in Newington recently tested positive for Covid-19

Source: seacoastcurrent.com See Less”

January 21, 2021 12:00 PM

“2 employees at Shoppers Drug Mart located on Mount Pleasant Road in Toronto recently tested positive for Covid-19

Source: dailyhive.com See Less”

January 21, 2021 12:00 PM

“45 employees at Home Depot located on North Figueroa Street in Cypress Park recently tested positive for Covid-19

Source: theeastsiderla.com See Less”

January 21, 2021 12:00 PM

“37 employees at Costco Wholesale located on Los Feliz Boulevard in Atwater Village recently tested positive for Covid-19

Source: theeastsiderla.com See Less”

January 21, 2021 12:00 PM

“14 employees at Lake Superior State University located on West Easterday Avenue in Sault Ste. Marie recently tested positive for Covid-19

Source: mlive.com See Less”

January 23, 2021 5:18 PM

“I lost $240k on Luckin Coffee, all my life savings. Now I'm broke af. I believed luckin was growing strong and becoming the next asia starbucks. I didn't know they could cheat on balance sheet, and had no idea about VIE structure and that a company can just fail in 3 months. From Nov to Jan did a 30... See More0% gain. I was just late to the party and entered at the wrong time, and played really badly.... I learned the lesson the hard way and I'm gonna just invest in etfs, gold and bonds for the rest of my hopefully long but quite useless life.

Source: Reddit See Less”

January 23, 2021 3:32 PM

“Luckin Coffee is a coffee retailer founded in 2017 based in Xiamen, the People’s Republic of China. Luckin Coffee owns and operates stores selling food and beverages, as well as a mobile application for food and beverage purchases.

On May 17, 2019, Luckin Coffee conducted an Initial Public Offer... See Moreing (“IPO”) of its ADSs.

On January 31, 2020, Muddy Waters Research published a report stating that Luckin Coffee had fabricated portions of its financial statements beginning in the third quarter of 2019, citing “smoking gun evidence” such as thousands of hours of store video, customer receipts, and monitoring of the Company’s mobile application data. On this news, the price of Luckin Coffee ADSs fell from $36.40 per share on January 30, 2020, to $32.49 per share on January 31, 2020.

On February 3, 2020, Luckin issued a press release denying Muddy Waters’s allegations. The Company “categorically denie[d] all allegations in the [Muddy Waters] Report” and assured investors that the “methodology of the Report is flawed, the evidence is unsubstantiated, and the allegations are unsupported speculations and malicious interpretations of events.”

On April 2, 2020, contrary to its previous denials, Luckin Coffee disclosed that it had conducted an internal investigation and had found that Luckin Coffee’s Chief Operating Officer Jian Liu and several of his direct reports had fabricated over $300 million of sales beginning in the second quarter of 2019. On this news, the price of Luckin Coffee ADSs fell from $26.20 per share on April 1, 2020 to $6.40 per share on April 2, 2020 – a decline of over 75%.

Luckin Coffee ADSs have now been delisted from trading on the NASDAQ. See Less”

December 31, 2020 11:24 AM

“Responding to an add on facebook I ordered and paid for a battery powered chainsaw on Dec. 13. I then received a confirmation email. On Dec. 30 I received an envelope the size of a cigarette pack containing a manual chainsaw. Where are the fact checkers when you need them? See Less”

January 11, 2021 10:53 PM

“I got the Oxford vaccine yesterday and I got a bit of a headache but then I went home and slept for most of the night and woke up with a migraine. Also, I had a fever from it. See Less”

January 13, 2021 4:58 PM

“Yes my little Angie was given a dream bone on Sept 26, 2020 at 7:30 pm at 8:pm she threw up the dream bone and then a few times with fluid and then collapsed on the floor her jaw was tight. I grabbed her up and rushed her to the vet. She had been poisoned by the dream bones her favourite treat. S... See Morehe started hemorraging blood out her butt, after transfusion it stopped around 4.30 am sept 27th then they called me to say her heart stopped and they revived her and she was on a ventolator and when I got there awww so sad poor thing. She was now bleeding in her lungs OH MY GOD. She passed away that morning. I cried for 2 and a half hours in the room with her dead I just could not bear to leave her. The vet bill was over 2400 dollars and she was gone in 12 hours after eating that stupid dream bone. I still have the package of treats. I bought them at Walmart. She was not even 2 years old yet. See Less”

December 30, 2020 10:00 PM

“Company name: Sportmix
Brand name: Sportmix
Product recalled: Dog and Cat Food
Reason of the recall: Elevated levels of aflatoxin
FDA Recall date: December 30, 2020
Recall details: Midwestern Pet Foods, Inc., of Evansville, IN is issuing a voluntary recall of the below-listed dog and cat food p... See Moreroducts due to tests indicating levels of Aflatoxin that exceed acceptable limits. Products were distributed nationally to online distributors and retail stores. Aflatoxin is a toxin produced by the mold Aspergillus flavus, which can grow on corn and other grains used as ingredients in pet food. At high levels, aflatoxin can cause illness and death in pets.

There have been reports of illnesses and deaths in dogs associated with the below listed lots of Sportmix High Energy. No cat or human illnesses have been reported. If your pet shows signs of aflatoxin poisoning including sluggishness, loss of appetite, vomiting jaundice (yellowish tint to the eyes, gums, or skin due to liver damage), and/or diarrhea, contact a veterinarian immediately. Provide a full diet history to your veterinarian. It may be helpful to take a picture of the pet food label, including the lot number. Lot code information may be found on the back of the bag and will appear in a three-line code, with the top line in the format “EXP 03/03/22/05/L#/B###/HH:MM” as follows (see below in pictures section).

Retailers and distributors should immediately pull recalled lots from their inventory and shelves. Do not sell or donate the recalled products. Retailers are encouraged to contact consumers who have purchased the recalled products if you have the means to do so (frequent buyer cards, etc.).

Pet parents: do not feed the recalled products to your pets or any other animals. Destroy the products in a way that children, pets, and wildlife cannot access them. Wash and sanitize pet food bowls, cups, and storage containers. Contact Midwestern Pet Foods Consumer Affairs at 800-474-4163, ext. 455 from 7AM to 4PM Central Time, Monday through Friday, or by email at info@midwesternpetfoods.com for additional information. This is a voluntary recall conducted in cooperation with the U.S. Food and Drug Administration.

Recalled lot codes are as follows:

- 50# Sportmix Energy Plus Lots Exp 03/02/22/05/L2, 03/02/22/05/L3, 03/03/22/05/L2
- 44# Sportmix Energy Plus Lots 03/02/22/05/L3
- 50# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 44# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 31# Sportmix Original Cat Lots 03/03/22/05/L3
- 15# Sportmix Original Cat Lots 03/03/22/05/L2, 03/03/22/05/L3

Products may be identified as follows (see pictures below).

Check the full recall details on fda.gov

Source: FDA See Less”

January 4, 2021 7:46 PM

“I ordered a hand held chain saw on Dec 12th 2020. I was v
Charged $40.89 .
What did come in the mail
Was a extra chain, but no saw See Less”

January 4, 2021 11:39 PM

“I ordered this saw on December 13th, on December 15th I recieved a confirmation notice the my purchase was on its way, today January 4th 2021 in the mail all I recieved was a chain. Is this a scam or what,and where is the rest of my purchased SAW????? See Less”

January 23, 2021 6:40 PM

“Anaphylaxis is a severe, life-threatening allergic reaction. It can occur after vaccination, but is rare.

The CDC released a report on Jan 17th 2021 stating that:

During December 21, 2020–January 10, 2021, monitoring by the Vaccine Adverse Event Reporting System detected 10 cases of anaphylax... See Moreis after administration of a reported 4,041,396 first doses of Moderna COVID-19 vaccine (2.5 cases per million doses administered). In nine cases, onset occurred within 15 minutes of vaccination. No anaphylaxis-related deaths were reported.

The implications for public health practice:

Locations administering COVID-19 vaccines should adhere to CDC guidance, including screening recipients for contraindications and precautions, having necessary supplies and staff members available to manage anaphylaxis, implementing recommended post-vaccination observation periods, and immediately treating suspected anaphylaxis with intramuscular epinephrine injection.

Source: CDC.gov See Less”

January 1, 2021 9:01 PM

“Company name: Precision Dose Inc.
Brand name: GUM Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 15 mL unit dose cups
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 31, 2020
Recall details: Company Announcement Precision Dose,... See MoreInc. is voluntarily recalling all lots of Chlorhexidine Gluconate Oral Rinse USP, 0.12%, 15mL Unit Dose Cups bearing an expiration date from 1/31/2021 – 02/28/2022 (see specific lots below) to the consumer level. Precision Dose, Inc. was notified by the manufacturer of the product, Sunstar Americas, Inc., that this product may be contaminated with the bacteria Burkholderia lata.

From information provided by the manufacturer, Sunstar Americas, Inc., use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such pneumonia and bacteremia.

To date, no adverse events have been reported to Precision Dose, Inc. related to this recall. The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and the product impacted is:

- Distributed in cases each containing 3 shrink-wrapped plastic trays each with 10 unit dose cups, 30-pack. NDC 68094-028-62
- Distributed in cases each containing 10 shrink-wrapped plastic trays each with 10 unit dose cups, 100-pack. NDC 68094-028-61

Chlorhexidine Gluconate Oral Rinse was distributed nationwide in the USA to pharmaceutical wholesalers. Precision Dose, Inc. is notifying its consignees directly and is arranging for return of all recalled product. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact Precision Dose, Inc. at 1 (800) 397-9228 (Monday-Friday, 8:00 AM to 4:30 PM Central Time) or by email to customercare@precisiondose.com. Consumers should contact their physician or healthcare provider if they have experienced problems that may be related to using this drug product. Affected products and lot numbers follow below: AFFECTED LOTS-Chlorhexidine Gluconate Oral Rinse USP, 0.12%

Check the full recall details on fda.gov

Source: FDA See Less”