Covid-19 OSHA Complaint, Walmart, 863 Harvest Ln, Williston, Vermont 05495, USA

3 years ago

Covid-19 OSHA Complaint, Walmart, 863 Harvest Ln, Williston, Vermont 05495, USA

863 Harvest Lane, Williston, 05495 Vermont, United States

Walmart Retail Store, Williston, Vermont:

Concerns over exposure to COVID-19.
Employer not allowing employees to wear facemasks while working.


Alleged Hazards: 2, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-04-09

#coronaviruscovid19 #osha #walmart #863harvestlane #williston #vermont #us

10

Related Reports

Starbucks Metallic Mugs recalled due to burn and laceration hazards, USA

3 weeks ago •source www.nestleusa.com

Recall notice

Nestlé USA has announced a recall of 440,500 Starbucks-branded ceramic mugs due to safety concerns. The mugs, which have a metallic coating, pose a burn and laceration hazard if microwaved or filled with extremely hot liquid. The company has reported 12 incidents of the mugs overheating or … See More
breaking, resulting in 10 injuries. Nestlé USA is currently working closely with the U.S. Consumer Product Safety Commission on this recall.

The recalled mugs were sold in two sizes, 11 oz. and 16 oz., as part of four different gift sets during the 2023 holiday season. They were distributed at Target, Walmart, and Nexcom (military retail outlets) across the U.S. from November 2023 to January 2024. The recall does not affect any other Nestlé USA or Starbucks-branded products.

- Starbucks Holiday Gift Set with 2 Mugs (11 oz.). Retailer: Target.
- Starbucks Classic Hot Cocoa and Ceramic Mug (16 oz.). Retailers: Walmart, Nexcom.
- Starbucks Peppermint and Classic Hot Cocoa Ceramic Mug (16 oz.). Retailer: Target.
- Starbucks Holiday Blend Coffee and Mug (16 oz.). Retailers: Walmart, Nexcom.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: www.nestleusa.com/media/pressreleases/metallicmugrecall
See Less

#target #walmart #nestle #starbucks #us

Starbucks Metallic Mugs recalled due to burn and laceration hazards photo #1
304
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user-wxcdd457

Anyone with any Sense, Knows that any metallic partial on Any container, will cause flames!! It’s not company’s fault. It’s the customers fault! Ignorance to the MAX!

Z

Package received - unknown recipient at my address, The Colony, TX

1 month ago •reported by user-zxmjr615

I received the package from Katie Sanchez, 135 Raritan Center Pkwy, Edison, NJ. Package was addressed to a name I don't know but at my address. I did not order anything from Walmart or Amazon. Package contained a pillow in the shape of a flower, appears to be gently used.

#unorderedpackage #delivery #amazon #walmart #thecolony #texas #us

Package received - unknown recipient at my address photo #1
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Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance, USA

1 month ago •source www.fda.gov

Recall notice

Brassica Pharma Pvt. Ltd. is voluntarily recalling the Eye Ointment products listed below with expiration dates ranging from February 2024 to September 2025. The products are being recalled due to a lack of sterility assurance. These products were distributed nationwide to wholesalers, retailers, and via the product … See More
distributors, Walmart, CVS, and AACE Pharmaceuticals Inc. To date, Brassica Pharma Pvt. Ltd. has not received any reports of adverse events up to 16th February 2024 related to this recall.

For those patients who use these products, there is a potential risk of eye infections or related harm. These products are intended to be sterile. Ophthalmic drug products pose a potentially heightened risk of harm to users because drugs applied to the eyes bypass some of the body’s natural defenses.

The affected products are:
- Product Name: Equate Lubricant Eye Ointment (Mineral Oil 42.5%, White Petrolatum 57.3%, Lanolin Alcohols), Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: Equate, NDC: 79903-026-35, UPC Code: 681131395298.
- Product Name: Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%, Microcrystalline Wax, Stearic Acid, Wheat Germ Oil), Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: Equate, NDC: 79903-028-35, UPC Code: 681131395304.
- Product Name: CVS Health Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%, Microcrystalline Wax, Stearic Acid Wheat Germ Oil, Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: CVS Health, NDC: 76168-707-35, UPC Code: 050428634141.
- Product Name: Lubricant PM Ointment, Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: AACE Pharmaceuticals, NDC: 71406-124-35, UPC Code: 371406124356.
For Lot number and expiry dates, you can visit the link below.

Brassica Pharma Pvt. Ltd. Is notifying its distributors AACE Pharmaceuticals Inc and its retailers Walmart and CVS. These distributors shall be further notifying the wholesalers and retailers via mail of this recall and arranging for return of all impacted products listed above. Consumers, distributors and retailers that have any product which is being recalled should cease distribution of the product. Consumers should stop using the recalled Eye Ointment and may return any of the above listed products to the place of purchase.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Brassica Pharma Pvt. Ltd.
Brand name: Multiple brands
Product recalled: Eye ointment products
Reason of the recall: Due to Potential Lack of Sterility Assurance.
FDA Recall date: February 26, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/brassica-pharma-pvt-ltd-issues-voluntary-nationwide-recall-equate-lubricant-eye-ointment-equate-stye
See Less

#cvspharmacy #recall #walmart #drugs #us

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance photo #1
303

H&Natural Brand Products - recalled due to Yellow oleander, USA

1 month ago •source www.fda.gov

Recall notice

San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native … See More
to Mexico and Central America. H&NATURAL TejoRoot and H&NATURAL Brazil Seed were distributed Nationwide to via internet on their site, Amazon.com, and Walmart.com. The company has received one report of gastrointestinal illness, including painful symptoms in conjunction with internal bleeding in connection with H&NATURAL TejoRoot, and has not received any reports of adverse events in connection with H&NATURAL Brazil Seed.

Risk Statement: Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

The recalled dietary supplements can be identified by the H&NATURAL logo and the following descriptions:
- Tejo Root, Raiz de Tejocte, H&Natural, Healthy, and Natural, Dietary Supplement, 10g pills, is packaged in a box or bottle, with UPC (196852946921)
- Brazil Seed Pure Natural Semilla de Brasil, H& Natural, Healthy and Natural, 0.167g seeds, packaged in a box or bottle, with UPC (195893047529) (196852820641) (195893698721) (195893236893)(196852134618) (195893336975)

Recalled lots are labeled with the following expiration dates, 3/24 and 5/24.

Consumers that have the recalled H&NATURAL TejoRoot or H&NATURAL Brazil Seed lots should stop using the products. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

In case you experience harm from extraneous materials, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: G.A. Mart dba H&Natural
Brand name: H&Natural
Product recalled: Brazil Seed Pure Natural Semilla de Brasil & Tejo Root, Raiz de Tejocte
Reason of the recall: Product contains yellow oleander, a poisonous plant
FDA Recall date: February 23, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ga-mart-issues-voluntary-nationwide-recall-hnatural-tejoroot-and-hnatural-brazil-seed-dietary
See Less

#amazon #walmart #dietarysupplements #recall #us

H&Natural Brand Products - recalled due to Yellow oleander photo #1
303
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I am reporting a seller in Walmart.com names Charles Kosanke., Antlers, OK, USA

3 months ago •reported by user-ddkz4334

I ordered a 4XL Tshirt from Walmart.com and received a size Large Tshirt from Charles Kosanke in Katy, TX. This shirt was NOT what I ordered. I've reported it with Walmart.com and the seller with no response.

#scam #onlineshopping #onlinescam #delivery #walmart #antlers #oklahoma #us

2
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Boil Water Advisory, West Noble Avenue, Williston, FL, USA

4 weeks ago

According to Williston City officials, a boil water notice has been issued after a water main broke on West Noble Avenue and has been repaired since Mar 16 in the morning. According to officials, the water system still needs time to pressurize.

Source: www.wcjb.com/2024/03/16/boil-water-notice-residents-williston/
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Boil Water Advisory, Williston, FL, USA

4 months ago

Authorities have issued a boil water advisory for customers in Williston after someone ran over a fire hydrant. The accident caused pipes to start leaking in two different places. Once water is restored, a boil water notice will go into effect for one week to 30 days … See More
until water quality is restored.

Source: www.wcjb.com/2023/11/30/boil-water-notice-effect-some-williston-residents/
Published: 2023-12-01
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#boilwateradvisory #williston #florida #us

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I purchased 5 of your large lighter smoking sets and none of them light., York, PA, USA

3 weeks ago •reported by user-wdvb9628

When I opened the first lighter, it flickered and then lit. When I tried to operate the other 4 lighters, none of them worked. Went back to the first lighter, and it.would not re-light. Plus the lighter boxes are very hard to open,,one of the box lids tore at the top. What do you suggest?

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Received package did not order., Willcox, Arizona, USA

3 weeks ago •reported by user-rknz8593

I received a package through U S Postage paid from this agency. The contents of the package was two thin metal wafer with a glue backing. I did not order any item from this dealer/agency.

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user-wxhfr592

Me too, same exact thing. Something is up

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Scam, Lexington, KY 40503, USA

2 weeks ago •reported by user-prkj4722

I did not get my parcel . In my mail box I just found parcel bag but bag was empty . Please find my parcel. I didn't get my parcel. When I check my mail box I just found empty parcel bag having usps tracking number 9261292700545500070679****. But where is my parcel?

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ForeverMen Natural Energy Boost - recalled due to undeclared allergens, USA

1 week ago •source www.fda.gov

Recall notice

FAonline INC, is voluntarily recalling all lots within expiry of the ForeverMen capsules to the consumer level. FDA analysis founds these products to be tainted with sildenafil and Tadalafil. Sildenafil/Tadalafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of sildenafil in the … See More
ForeverMen products renders them unapproved drugs for which safety and efficacy have not been established, therefor subject to recall. ForeverMen was distributed to consumers nationwide via the Internet. To date, Happy Together Inc. has not received any reports of adverse events related to this recall.

Risk Statements: Men with diabetes, high blood pressure, high cholesterol, or heart disease, may be on medications that if taken with these products could lower blood pressure to dangerous levels that could be life threatening. The products affected are men with diabetes, high blood pressure, high cholesterol, or heart disease.

The product is marketed as dietary supplements for male sexual enhancement and is packaged in a blister card. 10 count box. We are notifying the public through this public announcement due to lack of ability to identify customers who may have received the product. FAonline INC. is notifying its customers that have the ForeverMen products to stop use and properly discard the product.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: FAonline Inc
Brand name: ForeverMen
Product recalled: Natural Energy Boost
Reason of the recall: Product is tainted with sildenafil and tadalafil
FDA Recall date: April 02, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/forevermen-supplements-recalled
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ForeverMen Natural Energy Boost - recalled due to undeclared allergens photo #1
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