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Boil Water Advisory, Godby Branch Rd, Chapmanville, West Virginia 25508, USA

3 days ago

Godby Branch Road, 25508 West Virginia, United States

Boil water issued for Godby Branch and Wheatley Branch until further notice.

Source: twitter.com
Source publication date: 2021 11 23

89


Related Reports

PUD No. 1 of Clallam County is advising all water customers in Clallam Bay to boil their drinking water following the completion of the emergency water main construction along Highway 112 in accordance with Department of Health guidelines.

Source: twitter.com
Source publication date: 2021 11 23 See Less
8


Boil water from Stollings to Earling until further notice.

Source: twitter.com
Source publication date: 2021 11 23 See Less
89


A boil water advisory remains in effect for some customers of Waterworks District #3 in Iberia Parish.

The boil water advisory is in effect for the following areas:

Myers Road
Hunter Drive
Coteau Road from Coteau Elementary to Sandoz Road
Sandoz Road between Coteau Road and Hunter... See More Drive

Source: katc.com
Source publication date: 2021 11 24
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120


The City of Pennsboro has issued a boil water advisory for areas around Creed Collins School, Collins Ave, Reedwood St, Clayton St, to High St due to a water line break.

Source: twitter.com
Source publication date: 2021 11 24 See Less
8


Logan County PSD has issued a boil water advisory for all of Dog Patch/Laurel Wood Apts.

Source: twitter.com
Source publication date: 2021 11 24 See Less
89


City of Logan Water Dept. has issued a boil water advisory for Middleburgh to 3 Mile Curve including Logan County PSD.

Source: twitter.com
Source publication date: 2021 11 24 See Less
89


Bossier City issued a boil advisory Wednesday afternoon for portions of the city due to 4 water main breaks.

A contractor working near the city water main caused a break in Golden Meadows.

Three smaller mainline breaks from water flushing efforts happened in:

- The Robert E.... See More Lee Place neighborhood (Lillian St., Robert E. Lee St., Chaney St., and Loop St.)
- Near Waller Baptist Church (Patricia Drive between Bobbie St. and Waller Ave., Melanie Street, and Margaret Street from Melanie Street to Loreco Street).
- The 2500 Block of Melrose Avenue.

Source: arklatexhomepage.com
Source publication date: 2021 11 24
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71


Bossier City issued a boil advisory Wednesday afternoon for portions of the city due to 4 water main breaks.

A contractor working near the city water main caused a break in Golden Meadows.

Three smaller mainline breaks from water flushing efforts happened in:

- The Robert E.... See More Lee Place neighborhood (Lillian St., Robert E. Lee St., Chaney St., and Loop St.)
- Near Waller Baptist Church (Patricia Drive between Bobbie St. and Waller Ave., Melanie Street, and Margaret Street from Melanie Street to Loreco Street).
- The 2500 Block of Melrose Avenue.

Source: arklatexhomepage.com
Source publication date: 2021 11 24
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102


As a result of loss of pressure on a water main caused by a leak, a Boil Water Notice has been issued for water customers in South Elkins in the area bounded by Bond Lane, Ward Avenue, the Tygart River, and Whiteman Avenue.

Source: twitter.com
Source publication... See More date: 2021 11 24 See Less
38


As a result of loss of pressure on a water main caused by a leak, a Boil Water Notice has been issued for water customers in South Elkins in the area bounded by Bond Lane, Ward Avenue, the Tygart River, and Whiteman Avenue.

Source: twitter.com
Source publication... See More date: 2021 11 24 See Less
38


Recent Interesting Reports

Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... See More no illnesses reported to date.

During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.

The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.

The full list of affected products is on the link below.

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.

Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements

Check the full recall details on the FDA website: fda.gov

Source: FDA
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101


Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products.

Risk Statement: Benzene is... See More classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.

To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See the link below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically the ones listed in the link below.

The products were distributed nationwide in the United States through various retailers. Consumers, distributors, and retailers that have product which is being recalled should stop using or selling these specific Odor-Eaters® spray products and dispose of them appropriately.

Company name: Odor-Eaters®, owned by Blistex Inc.
Brand name: Odor-Eaters®
Product recalled: Oder Eaters spray products
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 17, 2021

Check the full recall details on fda.gov

Source: FDA
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101


FOR IMMEDIATE RELEASE – November 19, 2021 – American Screening LLC of Shreveport, Louisiana is voluntarily recalling 153,336 units of Hand Sanitizer, containing 70% ethyl alcohol gel to the consumer level. The hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk... See More of consumption.

Risk Statement: Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute. To date, American Screening LLC has not received any reports of adverse events related to this recall.

The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in an eight ounce bottle. The affected hand sanitizer lots include the following expiration dates of 5/21/2022 and 05/24/2022 for black capped bottles and no lot numbers or expiration dates for clear capped bottles. The product can be identified by its shape (small water bottle), with a black flip top cap or clear cap with blue pouring spout with the weight of measure of eight (8) ounces/237mL, UPC 8 4005051579 2.

The Hand Sanitizer was sold to customers & distributors Nationwide via the internet at americanscreeningcorp.com and/or in-house sales.

Consumers & distributors that have this hand sanitizer which is being recalled should stop distribution/use and return to place of purchase or discard. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to ingesting the hand sanitizer packaged in the 8 oz. water bottle style.

Company name: American Screening LLC
Brand name: American Screening
Product recalled: Hand Sanitizer
Reason of the recall: Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption
FDA Recall date: November 19, 2021

Check the full recall details on fda.gov

Source: FDA
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MaryRuth’s, a leading omni-channel health and wellness brand that offers vitamins, minerals, and supplements for the entire family, today announced that, out of an abundance of caution, it is voluntarily recalling two lots of its liquid probiotic for infants (1oz) due to the possibility of contamination by... See More Pseudomonas aeruginosa.

Pseudomonas aeruginosa is a microorganism found in the environment that, if ingested, can cause infection in immunocompromised individuals or, rarely, in very young infants. P. aeruginosa infections in immunocompromised infants are generally limited to hospital settings. In such settings, there is the chance that the infant’s immature gut will not be able to prevent P. aeruginosa from gaining access to the blood, and from there it can disseminate elsewhere in the body, resulting in the possibility of serious adverse health consequences.

This recall only affects two lots of the product, Lot #100420218 and Lot #100520218, UPC barcode number 856645008587. Lot numbers are located on the side of the bottle and on the bottom of the outer container in which the product is sold. No other lots or any other MaryRuth’s products are affected by this recall. This product is distributed nationwide through Target, Amazon, and direct sales from the company’s website.

The company is asking consumers to throw away product from both affected lot numbers. The company discovered the potential issue with one of its manufacturing partners during routine laboratory testing.

The only product complaint the company has received with respect to the affected product lots was one report of temporary diarrhea in an older infant after consuming the product, which the company does not believe was related to the presence of the microorganism.

Company name: MaryRuth’s
Brand name: MaryRuth’s
Product recalled: liquid probiotic for infants
Reason of the recall: Potential contamination with Pseudomonas aeruginosa
FDA Recall date: October 29, 2021

Check the full recall details on fda.gov

Source: FDA
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101


Package was supposed to be delivered November 6, 2021.
After days of endless calls finally told it left teterboro post office November 5 but was never delivered or tracked since. See Less
5.3K


The Procter & Gamble Company (NYSE: PG) is voluntarily recalling all lots with expiry through September 2023 of specific Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products sold in the United States, and listed in the table below, to the... See More consumer level due to the presence of benzene detected.

Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Based on exposure modeling and the cancer risk assessments published by the Environmental Protection Agency (EPA) (IRIS database), daily exposure to benzene in the recalled products at the levels detected in our testing would not be expected to cause adverse health consequences. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. To date, The Procter & Gamble Company has not received any reports of adverse events related to this recall and is conducting this recall out of an abundance of caution.

The affected products are used as antiperspirants and hygiene products and are packaged in aerosol cans. See the link below for Product names and UPC codes and images for further descriptions. They are recalling all lots with expiry through September 2023 of the products listed in the link below.

Company name: The Proctor & Gamble Company
Brand name: Old Spice Secret
Product recalled: Old Spice and Secret Aerosol Sprays
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 23, 2021

Check the full recall details on fda.gov

Source: FDA
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101


Usually is fine. Not this time. I decided to burn Nag Champa incense to meditate. As I was meditating, our dog started sniffling and then began throwing up large amounts of mucous. Her lips were swollen and pulled back slightly. She is ok now, but I've never... See More experienced anything like this using incense before this happened. I often use it for meditation. I called the vet who confirmed this is an allergic reaction and they informed me to monitor her and ensure she is safeand healthy, not vomiting anymore. They instructed me to open all the windows and doors, turn on ceiling fans,and run the furnace heat to pull remaining particulate into the HEPA filter on the furnace and then to replace the filter tomorrow to ensure it doesn't just recirculate the particulate if any happens to get through. Also said to wash hard surfaces in the room it was burned on and vacuum up any furniture,carpet, or rugs there to remove any settled particulate. I'm not sure what went wrong here. I've never had this happen with her or any other dog when burning this.

But even I am sniffling and nauseous after having burned it and my throat is sore. I took benedryl to
prevent an attack in me personally.

Product:
Nag Champa incense sticks.
Label information: Nag Champa Agarbatti Satya Sai Baba. Mfrs. Shrinivas
Sugandhalaya(BNG)LLP.1/9,8th Cross, Magadi Road, Bengaluru-560023, India. Certified green
product. Export Quality.2021 Series. Hand Rolled in India. UPC 8904245400491.Warning: insist for this label to avoid imitation buy from reputed dealers only. Earth. Contains seals with hologram over each side of the box with official logo. NetWt.40g. Quality assurance labels are not actual stickers demonstrating actual checks, but are instead printed onto the package to appear as if they were actual quality assurance stickers and are offset with a white background to trick a consumer. There are three which areas follows. Fake QA sticker1: Quality Assurance Management ISO 9001(check mark symbol)
Fake QA sticker2: Environmental Management ISO 14001(check mark symbol) Fake QA sticker 3: Occupational Health &
Safety OHSAS 45001 (check mark symbol).
Customer care number+917022000111

Item purchased at Archimage. Not their fault. They only buy reputable authentic items and this has to be a bad or contaminated batch here. | Symptoms: Nausea, Other
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279


I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT See Less
5.3K


CHICAGO, IL – November 19, 2021 - Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of four lots of Levetiracetam Injection, USP, to the user level. The lack of container closure integrity, found in reserve sample vials may result in a non-sterile product.

Risk Statement: Intravenous... See More administration of a product intended to be sterile that is not sterile could result in serious systemic infections which may be life threatening. 

To date, Sagent has not received reports of any product complaints or adverse events associated with this issue. Levetiracetam Injection, USP 500 mg per 5 mL, is used in the treatment of certain types of seizures and is packaged in a 5mL single-does vial. The Levetiracetam Injection, USP, label and affected lot numbers with Expiration Dates and NDC number can be found in the table below. 

Product: Levetiracetam Injection, USP / Lot Number: B0G85VB /Expiration Date: Jun-2022 / NDC Number: 25021-780-05 / Distribution Dates: May 2021 - August 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K88VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: March 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K89VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: August 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B1G194A /Expiration Date: Jun-2023 / NDC Number: 25021-780-05 / Distribution Dates: October 2021.

Product was distributed Nationwide from March to November  2021.

Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Levetiracetam Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: November 22, 2021

Check the full recall details on fda.gov

Source: FDA
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