Covid-19 OSHA Complaint, Walmart Stores Inc #2619, 910 Joe Mann Blvd, MIDLAND, MI, 48642, USA

2 years ago

Covid-19 OSHA Complaint, Walmart Stores Inc #2619, 910 Joe Mann Blvd, MIDLAND, MI, 48642, USA

910 Joe Mann Boulevard, Midland, 48642 Michigan, United States

1. Pink solution in clear plastic bottles used as disinfectant on checkout belts being used incorrectly by not allowing sufficient time to dry between customers. 2. Kayquat II Sanitizer seems strong, may be getting mixed with water at incorrect ratio. 3. Employees reacting to spray solutions, irritating some hands.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-22

#coronaviruscovid19 #osha #walmart #910joemannboulevard #midland #michigan #us

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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
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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!

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

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A package I did not order, Midland, MI, USA

1 month ago •reported by user-mtzx6294

I received a package with my name and address from “SECOND BROTHER” 166-10 Metcalf Ave Flushing NY 11365 on 2/23/24. I did not order it. I do not know how whoever this is got my name and address.

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user-yzdtb242

Have you ordered anything from fb or google ads but didn't receive item? Plenty of scams that you pay for something else but never get. They say you got it because they sent you that ring. Watch your credit card statements.

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Power Outage, Midland, MI, USA

2 months ago

There were reports of a power outage in Midland County. According to the Consumers Energy outage map, about 1,582 customers are affected by a power outage in the city of Midland on Friday afternoon Feb 9. The outage started at 2.22 p.m. The estimated time for restoration … See More
is 9:30 p.m. It’s unclear what prompted the outage. Crews are working to restore power to the area.

Outage link: www.consumersenergy.com/outagemap
Source: www.consumersenergy.com/
Published: 2024-02-09
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Power Outage, Midland, Midland County, TX, USA

4 months ago

According to Oncor's outage map, there are 2,429 customers affected by a power outage in Midland County on Wednesday morning Dec, 13. The outage affects the Midland area. There is no estimated time for restoration yet. It is unclear the cause of the outage.

Outage link: stormcenter.oncor.com/ … See More

Source: www.oncor.com/us/en/home.html
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Power Outage, Midland, MI, USA

4 months ago

Power outages have been reported near Grand Rapids due to high winds. The most affected areas are Alpine Township, Comstock Park, East Grand Rapids, and Grand Rapids Township. Additionally, the outage map shows power outages affecting 4,719 customers in Midland and 2,021 customers in Mio. Auburn with … See More
1,570 customers affected, and Sandford with 1,239 customers affected.'


Outage link: www.consumersenergy.com/outagemap
Source: www.wzzm13.com/article/news/local/power-outages-west-michigan/69-7da9ae3f-640c-40be-b81f-6bd5f0e64c4a
Published: 2023-12-09
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No way to return or exchange, Midland, TX, USA

5 months ago •reported by user-ftvv2979

I did order the dress I received but it is not the quality or description of what I ordered. There’s no way to return for a refund since the address on the label is a residential home that is not this company. No company name , the … See More
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user-wwpy6342

MY ADDRESS FOR THEM IS 746 GLASGOW AV ,INGLEWOOD CA 90301 !!!!BUT ITS RETURN CENTER NOT SHIPPING AS I CAN SEE

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AvKARE, LLC Atovaquone Oral Suspension - recalled due to potential Bacillus cereus contamination, USA

2 weeks ago •source www.fda.gov

Recall notice

AvKARE, LLC. is voluntarily recalling lot # AW0221A of Atovaquone Oral Suspension, USP 750mg/5mL to the Consumer/User level, due to the potential Bacillus cereus contamination in the product found during stability testing at a 3rd party lab. Atovaquone Oral Suspension, USP was distributed between 03/18/2024 through 03/21/2024 … See More
Nationwide to Wholesalers. To date, AvKARE has not received any reports of adverse events related to this recall.

Risk Statement: In the population most at risk, immunocompromised population, there is a reasonable probability that microbial contamination of Atovaquone Oral Suspension can result in disseminated, life threatening infections such as endocarditis and necrotizing soft tissue infections.

Atovaquone Oral Suspension, USP is indicated for prevention and treatment of Pneumocystis jiroveci pneumonia (PCP) in adults and children 13 years of age and older who cannot tolerate other medicines, such as trimethoprim-sulfamethoxazole.

The product is packaged in a carton. The identified NDC # associated with the product is 50268-086-12, UPC # 5026808612 and the affected lot# is AW0221A with an expiration date of 08/2025.

AvKARE, LLC is notifying its distributors and wholesale customers by mailings and email communications method and is arranging for returns of all recalled Atovaquone Oral Suspension, USP. Wholesalers who have Atovaquone Oral Suspension, USP 750mg/5mL, which are being recalled, should examine their inventory and cease dispensing, return any of the impacted lots to AvKARE, LLC. Consumers that have product which is being recalled should stop using the product and return it to place of purchase.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.  

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Company name: AvKARE, LLC
Brand name: AVpak
Product recalled: Atovaquone Oral Suspension, USP 750mg/5mL
Reason of the recall: Potential Bacillus cereus contamination
FDA Recall date: April 01, 2024

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Package not ordered, Tampa, FL, USA

3 weeks ago •reported by user-dxhj8163

Received a package 3/19/24, Full center in FL. A product I didn't order . Coincidentally I had a charge last week on my card and had it stopped and closed my card.
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user-wxxnw448

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