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Power Outage, Lewisburg, WV, USA

1 week ago

Lewisburg, 24901 West Virginia, United States

A scheduled power outage will occur on Wednesday, October 13.

Source: wvdn.mynews360.com
Source publication date: 2021 10 09

13


Related Reports

As of 11:40 p.m., FirstEnergy reported 430 customers without power in Cuyahoga County. There is also 126 without power in Ashtabula County, 347 without power in Lake County, 155 without power in Geauga County and 155 without power in Trumbull County.

Source: fox8.com
Source publication date: 2021... See More 10 21 See Less
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As of 11:40 p.m., FirstEnergy reported 430 customers without power in Cuyahoga County. There is also 126 without power in Ashtabula County, 347 without power in Lake County, 155 without power in Geauga County and 155 without power in Trumbull County.

Source: fox8.com
Source publication date: 2021... See More 10 21 See Less
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As of 11:40 p.m., FirstEnergy reported 430 customers without power in Cuyahoga County. There is also 126 without power in Ashtabula County, 347 without power in Lake County, 155 without power in Geauga County and 155 without power in Trumbull County.

Source: fox8.com
Source publication date: 2021... See More 10 21 See Less
503


Around 2 p.m. Thursday, Southern California Edison (SCE) officials were made aware of a power outage in Canyon Country, according to SCE’S outage map.
Initial reports were that a freight train had caused power lines to fall near the Santa Clarita Metrolink Station.
As of 3 p.m.... See More Thursday, about 1,439 residents are without power in the Canyon Country area.

Source: hometownstation.com
Source publication date: 2021 10 21
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A power outage affected 470 customers in Blocksburg

Source: lostcoastoutpost.com
Source publication date: 2021 10 22 See Less
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The entire Wymore community will experience a power outage Monday morning while maintenance is performed on a substation.
The power outage starts Monday, Oct. 25 and is expected to last at least three hours, though could be longer.

Source: beatricedailysun.com
Source publication date: 2021 10 22 See Less
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A crash in Greensboro Friday morning is causing power outages for hundreds of people.
As of 5:30 a.m., 893 Duke Energy customers are without power.

Source: wxii12.com
Source publication date: 2021 10 22 See Less
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The City of Lewisburg has issued a boil water advisory for Rolling Hills.

Source: twitter.com
Source publication date: 2021 09 29 See Less
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A boil water advisory has been issued by the City of Lewisburg.

Source: twitter.com
Source publication date: 2021 09 02 See Less
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Central Boaz PSD has issued a boil water advisory for all customers.

Source: twitter.com
Source publication date: 2021 10 22 See Less
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Recent Interesting Reports

Shipment arrived at Teterboro Center on 10/14. No movement since. Teterboro Center is located about 5 minutes from my house. 10/17 update says "Processing Exception, Other Delay Your shipment has potentially been delayed due to emergency or other conditions at 6:50 pm on October 17, 2021." See Less
5.1K


This is the 2nd package that just arrives at teterboro and just stops moving what’s the point of charging for next day air if you can’t get it done .. worse thing about this is that’s it’s anxiety medication i desperately need See Less
5.1K


HA
Hate USPS
I wonder if we could all group together and file a class action lawsuit. I saw another post here with two tracking #s stuck from October 1st and Sept 28th that haven’t moved yet.
Reply 1 week ago
Company name: Bryant Ranch Prepack
Brand name: Bryant Ranch Prepack
Product recalled: Methocarbamol 500mg
Reason of the recall: Bottles labeled as Methocarbamol 500mg tablets were found to contain Methocarbamol 750mg tablets.
FDA Recall date: October 19, 2021
Recall details: Burbank, CA, Bryant Ranch Prepack is voluntarily recalling... See More 1 lot of Methocarbamol 500mg, Tablets to the consumer level. The bottles labeled as Methocarbamol 500mg Tablets have been found to contain Methocarbamol 750mg Tablets.

Risk Statement: If a patient takes a 750mg Tablet of Methocarbamol instead of the prescribed 500mg Tablets, it potentially could result in Excessive Central Nervous System depression which may result in nausea, sedation, fainting, falls, seizure, coma, and death. Bryant Ranch Prepack has not received any reports of adverse events related to this recall.

The product is used together with rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions and is packaged in a white round bottle with a red and white label, which reads Methocarbamol 500mg packaged in counts of 30 (NDC:7133517952), 60 (NDC: 7133517954), and 90 (NDC:7133517957) pills. The affected Methocarbamol 500mg lots include the following Lot Number 163935/ Exp. Date 10/22. The product can be identified by red and white label with a yellow border at the top and bottom of the label, top of the label reads “Packaged by Bryant Ranch Prepack”, labels are pictured below. The Methocarbamol 500mg was distributed Nationwide to multiple physician offices.

Bryant Ranch Prepack is notifying its distributors and customers by letter and email and is arranging for return of all recalled products. Consumers that have the bottles labeled as Methocarbamol 500mg Tablets which is being recalled should stop using immediately and return to place of purchase and/or contact their physician. Distributors/Physicians should stop distribution and contact Bryant Ranch Prepack to return the product immediately.

Check the full recall details on fda.gov

Source: FDA
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Shipment was supposed to arrive Friday.  Now I received the following message : Your shipment has potentially been delayed due to emergency or other conditions at 6:46 pm on October 17, 2021. | Symptoms: Other See Less
5.1K


GR
Grinsler
Same here. Mine arrived at Teterboro 10/14 @ 3:35 pm. 10/17 update says "Processing Exception, Other Delay Your shipment has potentially been delayed due to emergency or other conditions at 6:50 pm on October 17, 2021."
Reply 5 days ago
MI
Mitch
Same very important documents are there What the hell is going on
Reply 2 days ago
October 11, 2021 – Tuffy's Pet Foods is issuing a voluntary recall of approximately 1,600 cases of Pure Vita Salmon Entree Dog Food in a Tetrapak carton following notification from the product manufacturer of potentially elevated levels of Vitamin D. No illnesses or injuries have been reported... See More from consumers to date.

Consuming elevated levels of vitamin D in dog food can cause adverse reactions in dogs of all sizes, including symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. When ingested at excessive levels, vitamin D can lead to serious health issues in dogs including renal dysfunction. While no reports of illness or injury have been reported from consumers to date, Tuffy’s is acting out of an abundance of caution and is removing the specific lots of product listed below from distribution.

Consumers should stop feeding the product listed below to their pets immediately. Tuffy’s recommends consumers whose dogs have consumed the potentially affected product and are exhibiting any of the above-mentioned symptoms contact their veterinarian.

- Pure Vita Salmon Entrée Dog Food TetraPak (12.5 oz. per carton). UPC: 0 73893 96202 1. Lot numbers: 0629101N1 /
0901101N1. Best By dates: 29 Jun 2023 / 1 Sep 2023.

The recalled product was distributed exclusively within the United States to distributors and retail stores.  The recalled product is limited to Pure Vita Salmon Entrée Dog Food in a Tetrapak carton, bearing UPC Code "0 73893 96202 1" (found on side of the carton).  Products included in the recall are identified by the "Best by Dates" and “Lot Numbers” (found on the top of the carton) as listed above. No other Pure Vita dog or cat foods, or treats are affected by this announcement.

Consumers who purchased the Pure Vita Salmon Entrée dog food product subject to this voluntary recall (as identified above) are urged to return the product to their retailer for a full refund.

For consumer information or questions regarding this voluntary recall, please contact Tuffy’s Pet Foods, Inc. at (800) 525-9155 from Monday-Friday, 8:00am-5:00pm Central Time

Company name: Tuffy’s Pet Foods, Inc.
Brand name: Nutri Source
Product recalled: Pure Vita Salmon Entrée Dog Food
Reason of the recall: Elevated Levels of Vitamin D
FDA Recall date: October 12, 2021

Check the full recall details on fda.gov

Source: FDA
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1 Share


I was a premium TokyoTreat subscriber for 6 months, 35$/month, I got only 2 boxes, first when I subscribed, last one after I unsubscribed. Looks like real scam to me, they steal my money See Less
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FROMM FAMILY FOODS is issuing a voluntary recall of approximately 5,500 cases of Fromm Shredded can Entrée dog food due to potentially elevated levels of Vitamin D.

Consumers should stop feeding the products listed below to their dogs. Potential adverse reactions could occur in all size dogs. ... See More No reports of illness or injury have been reported from consumers to date, however Fromm management has determined it is prudent to pull these four lots out of distribution.

Affected recalled products were distributed at neighborhood pet stores nationwide.

Products are packaged in 12 oz. cans with Best By Date 08/2024. A full list of affected products is:
- Four-Star SHREDDED BEEF IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11877, 12 oz. per can, UPC: 7270511876, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11881, 12 oz. per can, UPC: 7270511880, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11879, 12 oz. per can, UPC: 7270511878, Best By Date 082024
-Four-Star SHREDDED TURKEY IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11883, 12 oz. per can, UPC: 7270511882, Best By Date 082024

Dogs ingesting elevated levels of Vitamin D may exhibit symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. Vitamin D when consumed at very high levels can lead to serious health issues in dogs including renal dysfunction. Consumers who have dogs that have consumed any of the affected products and are exhibiting these symptoms should contact their veterinarian.

Check the full recall details on fda.gov

Company name: Fromm Family Foods
Brand name: Fromm Four-Star Nutritionals
Product recalled: Shredded Entrée canned dog food
Reason of the recall: Elevated levels of Vitamin D
FDA Recall date: October 01, 2021

Source: FDA
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Coppertone, owned by Beiersdorf, is voluntarily recalling specific lots of five Coppertone aerosol sunscreen spray products manufactured between the dates of January 10, 2021 and June 15, 2021 to the consumer level.  Coppertone has identified the presence of benzene in these lots of products Twelve lots of... See More Coppertone spray products are impacted by this voluntary recall, specifically:

- Product Description: CT P&S BABY SPF50 SPRAY 5OZ 12S . Lot: TN0083J UPC: 72140028817. Manufacturing Date: 44470.
- Product Description: CT P&S BABY SPF50 SPRAY 5OZ 12S . TN0083J: TN0083K 72140028817: 72140028817. Manufacturing Date: 44501.
- Product Description: CT P&S KIDS SPF50 SPRAY 5OZ 12S . TN0083K: TN00854 72140028817: 72140028824. Manufacturing Date: 44531.
- Product Description: CT P&S KIDS SPF50 SPRAY 5OZ 12S . TN00854: TN00855 72140028824: 72140028824. Manufacturing Date: 1/14/2021.
- Product Description: CT SPORT MIN SPF50 SPRAY 5OZ 12S . TN00855: TN008KU 72140028824: 72140028701. Manufacturing Date: 3/15/2021.
- Product Description: CT SPORT MIN SPF50 SPRAY 5OZ 12S . TN008KU: TN008KV 72140028701: 72140028701. Manufacturing Date: 3/16/2021.
- Product Description: CT P&S SPF50 SPRAY 5OZ 12S . TN008KV: TN00BR2 72140028701: 72140028800. Manufacturing Date: 3/31/2021.
- Product Description: CT P&S BABY SPF50 SPRAY 5OZ 12S . TN00BR2: TN009GH 72140028800: 72140028817. Manufacturing Date: 3/31/2021.
- Product Description: CT P&S KIDS SPF50 SPRAY 5OZ 12S . TN009GH: TN00857 72140028817: 72140028824. Manufacturing Date: 44351.
- Product Description: CT SPORT SPRAY SPF50 1.6OZ 24S . TN00857: TN00BU3 72140028824: 41100005069. Manufacturing Date: 44352.
- Product Description: CT P&S SPF50 SPRAY 5OZ 12S . TN00BU3: TN00CJ4 41100005069: 72140028800. Manufacturing Date: 6/15/2021.
- Product Description: CT P&S KIDS SPF50 SPRAY 5OZ 12S . TN00CJ4: TN00CJV 72140028800: 72140028824. Manufacturing Date: 6/15/2021.

Benzene is classified as a human carcinogen. Exposure to benzene can occur through inhalation, oral, and skin and it could, depending on the level and extent of exposure, result in an increased risk of cancers including leukemia, and blood cancer of the bone marrow and other blood disorders which can be life-threatening.

Daily exposure to benzene at the levels detected in these affected Coppertone aerosol sunscreen spray products would not be expected to cause adverse health consequences based on generally accepted exposure modeling by numerous regulatory agencies.

Out of an abundance of caution, we are recalling certain lots of these specific aerosol sunscreen spray products. To date, Coppertone has not received any reports of adverse events related to this recall.

The voluntarily recalled sunscreen spray products are packaged in aerosol cans. The products were distributed nationally in the United States through various retailers. Consumers should stop using these specific Coppertone aerosol sunscreen spray products and dispose of them appropriately.

Coppertone is also notifying its retailers by letter and is arranging for returns of all voluntarily recalled lots of sunscreen spray products. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these aerosol sunscreen spray products.

The FDA and other medical authorities recognize the public health benefits of sunscreens and strongly advise the use of sunscreen along with other protective measures from the sun.

Company name: Coppertone, owned by Beiersdorf
Brand name: Coppertone
Product recalled: Coppertone aerosol sunscreen spray products
Reason of the recall: Presence of benzene
FDA Recall date: September 30, 2021

Check the full recall details on fda.gov

Source: FDA
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The FSAI announced the recall of certain batches of Emergen-C Energy Release and Immunity Support Food Supplement due to the presence of the unauthorized pesticide ethylene oxide. Ethylene oxide is a pesticide that is not permitted for use in foods sold in the EU but is approved... See More for use by other countries outside the EU.

The recalled products are:
- Emergen-C Energy Release & Immunity Support Super Orange, Mega Pack 24 sachets, Lot # FUB03, Best before 01/24.
- Emergen-C Energy Release & Immunity Support Super Orange, Mega Pack 24 sachets, Lot # NT489, Best before 10/23.
- Emergen-C Energy Release & Immunity Support Super Orange, 8 sachets, Lot # GU393, Best before 10/23.

Although the consumption of the contaminated product does not pose an acute risk to health, there is an increased risk if there is continued consumption of contaminated food over a long period of time. Therefore, exposure to this substance needs to be minimised.

For more recall details check on FSAI website: fsai.ie

Source: FSAI
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