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Walmart
Updated: January 14, 2021 12:00 PM
Covid-19 OSHA Complaint, WALMART SUPERCENTER, 1550 W Newlands Dr E, FERNLEY, NV, 89408, USA
WALMART SUPERCENTER, 1550 W Newlands Dr E, FERNLEY, NV, 89408, USA
January 14, 2021 12:00 PM
“1. Failure to comply with the mandate for employees to wear face coverings. The night shift employees never wear face coverings during merchandise stocking and supervisors are not enforcing the mandate. 2. Failure to comply with social distancing measures by maintaining a minimum six-foot distance b... See Moreetween employees in public spaces. The employer is not enforcing social distancing between employees during the night shift. 3. Failure to comply with the mandate for persons/patrons to wear face coverings while in the Employer's business establishment. The employer is not enforcing the mandate requiring patrons to wear face coverings before entering the store. 4. The store is not being sanitized as required during the night shift and throughout the day to prevent the potential spread of COVID-19. 5. Employees are being retaliated against if they approach supervisors to express concerns related to safety and/or health related to the current pandemic.
Alleged Hazards: 5, Employees Exposed: 50
Source: Osha.gov | Receipt Date: 2020-12-11 See Less”
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Covid-19 OSHA Complaint, Walmart, 2900 Main Street, SUSANVILLE, CA, 96130, USA
Walmart, 2900 Main Street, SUSANVILLE, CA, 96130, USA
January 14, 2021 12:00 PM
“3205: Employer not enforcing that customers wear facial coverings.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-15 See Less”
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Covid-19 OSHA Complaint, Walmart Supercenter #2537, 1515 Dana Drive, REDDING, CA, 96003, USA
Walmart Supercenter #2537, 1515 Dana Drive, REDDING, CA, 96003, USA
January 14, 2021 12:00 PM
“3205: Social Distancing is not being enforced.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-14 See Less”
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Covid-19 OSHA Complaint, Walmart, 2717 Rock Island Place, BISMARCK, ND, 58504, USA
Walmart, 2717 Rock Island Place, BISMARCK, ND, 58504, USA
January 14, 2021 12:00 PM
“For employees potentially exposed to COVID-19 infections from employees with confirmed COVID-19 positive test result being allowed to work.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-08-03 See Less”
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Covid-19 OSHA Complaint, Walmart Supercenter, 2200 17th Street, SPIRIT LAKE, IA, 51360, USA
Walmart Supercenter, 2200 17th Street, SPIRIT LAKE, IA, 51360, USA
January 14, 2021 12:00 PM
“1. Employer is not cleaning and disinfecting the entire store to follow COVID protocols. 2. Break rooms, registers, and other employee areas not cleaned regularly to keep employees safe.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-08 See Less”
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Covid-19 OSHA Complaint, WALMART NEIGHBORHOOD MARKET, 45 Sutters Mill Road, SAINT PETERS, MO, 63376, USA
WALMART NEIGHBORHOOD MARKET, 45 Sutters Mill Road, SAINT PETERS, MO, 63376, USA
January 14, 2021 12:00 PM
“Employee is exposed to hazardous chemicals causing irritation face, eyes and skin Employees are not provided information concerning chemicals they are exposed to Employee is exposed to heat hazards Employees are exposed to struck by hazards due to the cart return opening not being properly marked /... See Moremitigated as hazard.
Alleged Hazards: 4, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-12-08 See Less”
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Covid-19 OSHA Complaint, Walmart, 190 E. Round Grove Rd., LEWISVILLE, TX, 75067, USA
Walmart, 190 E. Round Grove Rd., LEWISVILLE, TX, 75067, USA
January 14, 2021 12:00 PM
“Recommended CDC guidelines are not being followed where several out breaks of COVID has occurred with staff members.
Alleged Hazards: 1, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2020-12-09 See Less”
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Covid-19 OSHA Complaint, Walmart Supercenter #524, 200 Business Park Blvd, KENEDY, TX, 78119, USA
Walmart Supercenter #524, 200 Business Park Blvd, KENEDY, TX, 78119, USA
January 13, 2021 12:00 PM
“1. Employees are not being informed of potential exposures to Covid-19 when other employees have tested positive. 2. The employer is not conducting daily health screenings. 3. The employer is not conducting routine cleaning or deep cleaning after notification of positive cases. 4. The employer is no... See Moret enforcing the facial covering policy.
Alleged Hazards: 4, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2020-12-16 See Less”
Helpful
Covid-19 OSHA Complaint, Walmart, 929 S Pine St, VIVIAN, LA, 71082, USA
Walmart, 929 S Pine St, VIVIAN, LA, 71082, USA
January 13, 2021 12:00 PM
“Eight to nine people have contracted COVID at work. When tested Positive Store Manager made them continue working which resulted in more positive results for others.
Source: Osha.gov | Receipt Date: 2020-11-04 See Less”
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Covid-19 OSHA Complaint, Walmart, 10617 East Washington Street, INDIANAPOLIS, IN, 46229, USA
Walmart, 10617 East Washington Street, INDIANAPOLIS, IN, 46229, USA
January 13, 2021 12:00 PM
“Employer not enforcing social distancing|Other not following CDC guidelines of distancing -- allowing anyone and everyone in store -- have constant traffic inside store -- something needs to be done
Source: Osha.gov | Receipt Date: 2020-04-14 See Less”
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Recent Interesting Reports
Moderna COVID-19 Vaccine, no symptoms yet., Long Island City, Queens, NY, USA
Long Island City, Queens, NY, USA
January 14, 2021 8:51 PM
“I am a teacher and am authorized to get the Moderna vaccine. I made an appointment in Ridgewood 2 days ago. Appoint was at 5:20 but didn't get my shot until 7:40. The lines are extremely long at night. But the nurse said they are empty in the morning. Once you get inside it is very fast, everyone is... See Morevery helpful and you can sign up for your second vaccine. They make you wait 15 mins to make sure you're ok before you leave. I have no side effects from the shot and feel fine. See Less”
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January 8, 2021 6:01 PM
“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... See Morelac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.
Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.
Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.
Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019
Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lot, and to return the product to Fresenius Kabi.
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”
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Totally false advertising. Blackcass.com Chainsaw, Orlando, FL, USA
Orlando, FL, USA
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”
Helpful
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”
Helpful
1 person found this review helpful
BlackCass hand-held saw, Jackson, Ohio, USA
Jackson, Ohio, USA
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”
Helpful
January 14, 2021 11:44 AM
“I wonder how many people were duped by this disreputable company! Guess I should know better than to order from a company I know nothing about! Shame on them for taking hard earned money during this day and time. And shame on Facebook for allowing them to advertise. See Less”
Helpful
1 person found this review helpful
Sent wrong item and is a bad item!, Langlois, OR, USA
Langlois, OR, USA
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”
Helpful
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”
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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”
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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”
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