Covid-19 OSHA Complaint, TSPA NW LLC, 3702 S Fife St, Tacoma, WA 98409, USA

December 5, 2020 12:00 PM

3702 South Fife Street, Tacoma, 98409 Washington, United States

Alleged Hazards: - Employer has not disinfected work areas of employees who tested positive for COVID-19 and is demanding other employee to work in the infected area as soon as sick employee leaves.


Source: Osha.gov | Receipt Date: 2020-10-16

January 17, 2021 12:00 PM

“An employee at Braden River High School located on East State Road 70 in Bradenton recently tested positive for Covid-19

Source: bradenton.com See Less”

January 17, 2021 12:00 PM

“81 staff members and 102 students at Cypress-Fairbanks Independent School District located in TX recently tested positive for Covid-19

Source: communityimpact.com See Less”

January 17, 2021 12:00 PM

“An employee at McDonald's located on 160 St in Surrey recently tested positive for Covid-19

Source: burnabynow.com See Less”

January 17, 2021 12:00 PM

“6 employee at New London City Public Works located on Union St in New London recently tested positive for Covid-19

Source: theday.com See Less”

January 17, 2021 12:00 PM

“An employee at Howard County Library System HCLS located on Glenwood Branch in Cooksville recently tested positive for Covid-19

Source: patch.com See Less”

January 17, 2021 12:00 PM

“An employee at Starbucks located on North H Street in Lompoc recently tested positive for Covid-19

Source: ksby.com See Less”

January 17, 2021 12:00 PM

“An employee at Sobeys Ira Needles located on Ira Needles Boulevard in Kitchener recently tested positive for Covid-19

Source: kitchenertoday.com See Less”

January 18, 2021 9:47 PM

“Customers aren’t wearing masks at all! This is a county wide mandate in Maricopa! See Less”

January 14, 2021 12:00 PM

“Alleged Hazards: - Employer is not enforcing the wearing of masks to protect employees from COVID-19 as per the Governor's COVID-19 guidelines.


Source: Osha.gov | Receipt Date: 2020-11-23 See Less”

January 14, 2021 12:00 PM

“employer removing masks in the Airbnb, not enforcing masks to be worn in clients homes, employer coming to work sick during the pandemic, no restrooms are provided at the 1006 N Yakima place since March, black mold and mildew in the storage closet.


Source: Osha.gov | Receipt Date: 2020-12-01 See Less”

January 17, 2021 11:59 PM

“The FSA announced the recall of several dog food products by Mars Petcare UK because they may contain high levels of vitamin D which exceed the maximum permitted intake.

FSA advises pet owners that if they have bought any of the following dog food products, you should stop feeding them to your do... See Moreg and contact Mars Petcare Customer Service at 0800 013 3131. If you have concerns that your pet may be showing symptoms of illness after eating one of the affected products, please contact a veterinarian.

- CHAPPIE Complete Chicken & Wholegrain Dry Dog Food (3kg). Batch code: 045F9MIN05. Best before: 44692
- PEDIGREE Mixer Adult Dry Dog Original (3kg). Batch code: 046E9MIN05 | 046F9MIN05 | 048A9MIN05. Best before: 12 February 2022 | 20 February 2022 | 22 February 2022
- PEDIGREE Mixer Adult Dry Dog Food Original (10kg). Batch code: 046E9MIN08 | 047C9MIN08. Best before: 12 February 2022 | 17 February 2022
- PEDIGREE Adult Complete Dry Dog Food with Chicken & Vegetables (12kg). Batch code: 046C9MIN08 | 046D9MIN08 | 046E9MIN08. Best before: 10 February 2022 | 11 February 2022 | 12 February 2022
- PEDIGREE Adult Complete Dry Dog Food with Chicken & Vegetables (2.6kg). Batch code: 045F9MIN05 | 047A9MIN05. Best before: 06 February 2022 | 15 February 2022

High levels of vitamin D fed to a pet over a short period (weeks/months) should not cause undue concern. Over a longer period of feeding, ingestion of elevated levels can lead to potential dog health issues. Vitamin D, when consumed at very high levels, can lead to serious health issues in dogs including renal dysfunction.

Check the full recall details on the FSA website food.gov.uk

Source: FSA See Less”

January 7, 2021 1:49 PM

“BlackCass. I ordered a hand-held saw and received only an extra chain. Can I get a refund? See Less”

December 30, 2020 9:21 AM

“The FDA is alerting pet owners and veterinary professionals about certain Sportmix pet food products manufactured by Midwestern Pet Foods, Inc. that may contain potentially fatal levels of aflatoxin. As of December 30, 2020, 28 deaths and 8 illnesses in dogs that ate the recalled product have been r... See Moreeported. This is an ongoing investigation. Case counts and the scope of this recall may expand as new information becomes available.

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. Pets experiencing aflatoxin poisoning may have symptoms such as sluggishness, loss of appetite, vomiting, jaundice (yellowish tint to the eyes or gums due to liver damage), and/or diarrhea. In severe cases, this toxicity can be fatal. In some cases, pets may suffer liver damage but not show any symptoms.

Pet owners should stop feeding their pets the recalled products listed below and consult their veterinarian, especially if the pet is showing signs of illness. The pet owner should remove the food and make sure no other animals have access to the recalled product. Sanitize pet food bowls, scoops, and storage containers using bleach, rinsing well afterwards with water, and drying thoroughly. There is no evidence to suggest that pet owners who handle products containing aflatoxin are at risk of aflatoxin poisoning.

Midwest Pet Food, Inc. already recalled the following lots of Sportmix pet food products:
- Sportmix Energy Plus, 50 lb. bag. Lots: Exp 03/02/22/05/L2 | Exp 03/02/22/05/L3 | Exp 03/03/22/05/L2
- Sportmix Energy Plus, 44 lb. bag. Lot: Exp 03/02/22/05/L3
- Sportmix Premium High Energy, 50 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Premium High Energy, 44 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 31 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 15 lb. bag. Lots: Exp 03/03/22/05/L2 | Exp 03/03/22/05/L3

Check the full outbreak announcement 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 10:32 PM

“Totally false advertising. I order two chainsaws and got two open 26" chains with straps on both ends. Not happy. This advertising was misleading and took over 30 days to receive this product in the mail. I am totally dissatisfied with this purchase and company. See Less”

December 28, 2020 8:00 PM

“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 28, 2020
Recall details: Schaumburg, Illinois, Sunstar Americas, I... See Morenc. (SAI) is voluntarily recalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 12/31/2020 – 9/30/2022 to the consumer level. This product may be contaminated with the bacteria Burkholderia lata. This is an expansion of the recall initially announced on October 27, 2020. 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 as pneumonia and bacteremia.

To date, 29 adverse events have been reported to SAI related to this recall. Affected patients tested positive for Burkholderia lata infections, typically found in sputum cultures while under treatment for other serious medical conditions. Use of the contaminated product on patients with pre-existing respiratory conditions, including those infected with Covid-19, is particularly unsafe.

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 is packaged as follows:

- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.

The product can be identified as shown in the images below Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers follow below:

-Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 16 fl.oz. Amber Bottles. NDC #: 052376-021-02. Product Code: 1789P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022

- Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 4 fl.oz. Amber Bottles NDC #: 052376-021-04. Product Code: 1788P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. Sunstar is committed to delivering safe, fully compliant products of the highest quality and is taking necessary steps to prevent future occurrence of this issue. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA See Less”

January 5, 2021 5:07 PM

“I ordered a Skil handheld battery operated chainsaw and after several weeks received a pocket chainsaw in a small pouch. Never in any of the advertisements for the chainsaw that I ordered were there pictures of the pocket chainsaw I received. I even used PayPal to protect myself. This is clearly a... See Morescam and they need to be held accountable. This was Christmas present for someone and not only was it late, now it's not even what I ordered!! See Less”

January 16, 2021 3:36 PM

“I ordered a Stihl wood cutter and got an IWORKS mini chain saw that does not work. See Less”

December 23, 2020 10:00 PM

“Company name: Shane Erickson, Inc. DBA Innovative Marketing Consultants
Brand name: IMC
Product recalled: Wash-Free Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: December 23, 2020
Recall details: Shane Erickson, Inc. is voluntarily recalling lot 2020/05/11 and MFG:... See More2020/05/10 L/N: 20200510-3 of imc Wash-Free Hand Sanitizer 50 ml, 100 ml, 300 ml and Wash Free Hand Sanitizer 300 ml lot 2020/05/11 and Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml lot 2020/05/11 listed in the table below to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, Shane Erickson, Inc. has not received any reports of adverse events related to the product(s) of this recall. Recalled Products:

- IMC Wash-Free Hand Sanitizer 50 ml, 1.7 oz (8 19845 00597 8). Lot: 43962. Expiration date: 45056
- IMC Wash-Free Hand Sanitizer 100 ml, 3.4 oz (8 19845 00598 5). Lot: MFG: 2020/05/10 L/N: 20200510-3. Expiration date: N/A
- IMC Wash-Free Hand Sanitizer | Wash-Free Hand Sanitizer | Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml, 10.14 oz (8 19845 00599 2). Lot: 43962. Expiration date: 45056

The product is used as a hand sanitizer for handwashing to decrease bacteria on the skin when soap and water are not available. All products are packaged in a plastic bottle. The 50 ml are in a HDPE opaque white bottle with a blue cap, the 100 ml is in a clear PET bottle with a clear cap and the 300 ml are in a clear PET bottle with a black pump. The product can be identified by checking the product size, UPC details, lot number and expiration date on the bottle containing the product. The product can also be identified by this information on the back label: Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, YUEWEIXIAOZHENGZI (2020) - 04 - No. 0023.

Some of the product has custom front labels (see examples below) the back label on the custom labels have the same identification information as previously mentioned above. The hand sanitizer was distributed Nationwide in the USA to wholesale and retail customers.

Shane Erickson, Inc. is notifying its distributors and customers by mail/email and is arranging for the return of all recalled products. Consumer, distributors, and retailers that have product, which is being recalled, should stop use or distribution and return to place of purchase. Consumers with questions regarding this recall can contact Shane Erickson, Inc. by phone at 952.252.1254 [Call: 952.252.1254] or email sales@imcsuccess.com Monday through Friday from 8:00 am to 5:00 pm Central Time Zone.

Check the full recall details on fda.gov

Source: FDA See Less”

January 8, 2021 12:49 PM

“On December 14, 2020 I ordered the Blackcass battery operated chainsaw. On January 8, 2021 I received a chain with two handles attached. See Less”