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Power Outage, Buncombe County, NC, USA

1 year ago

North Carolina, United States

More than 3,000 Western North Carolina residents were left without electricity Friday afternoon after strong storms. According to the Duke Energy Outage Map, about 3,300 customers were without power Reported outages by county: Avery: 59Buncombe: 318Burke: 1Cherokee: 108Graham: 173Haywood: 76Henderson: 6Jackson: 87Macon: 463Madison: 33McDowell: 1Mitchell: 3Polk: 7Rutherford: 73Swain: 1,876Transylvania: 16

Outage link: outagemap.duke-energy.com/#/current-outages/ncsc
Source: www.erienewsnow.com/story/46441735/storms-bring-hail-downed-trees-and-power-outages-to-western-north-carolina
Published: 2022-05-07

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Colorado Springs Utilities reported about 1,199 customers without electricity in downtown Colorado Springs on Thursday afternoon, Mar 28. The outage started at 3:57 p.m. The estimated time for restoration was listed at 7:47 p.m. The cause of the outage was not determined. Power has been already restored... See More to the area.

Outage link: s3.amazonaws.com/outagemap.csu.com/external/default.html
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According to The Public Service Company of Oklahoma, a power outage in north Tulsa on March 28 affected more than 15,000 customers after a transmission line equipment failure. Crews worked to fix the issue. Power was restored at about 2:00 p.m.

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Outage link: outagemap.ma.nationalgridus.com/
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Outage link: www.outagemap-xcelenergy.com/outagemap/?state=CO
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A Walmart in southeast Missouri was closed due to a power outage. According to a post on the Poplar Bluff Walmart social media page, the location is closed until further notice. According to the outage map, power was restored to the area.

Outage link: ebill.ozarkborder.org/maps/OMSWebMap/
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There were reports of a power outage in Charlotte. Duke Energy reported about 460 customers without electricity in the Sardis Woods area in Charlotte on Thursday afternoon, Mar 28. The outage started at 2:42 p.m. The estimated time for restoration is 6:30 p.m. The outage was caused... See More by an object coming into contact with power lines. Crews are working to safely restore power to the area.

Outage link: outagemap.duke-energy.com/#/current-outages/ncsc
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Outage link: outagemap.duke-energy.com/#/current-outages/ncsc
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Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulates in the product... See More solution. The lot was distributed nationwide to wholesalers and hospitals from June 16, 2022, through October 17, 2022. To date, Par has not received any reports of adverse events related to this recall.

Administration of an injectable product that contains particulate matter may result in local irritation or swelling in response to the foreign material. If the particulate matter reaches the blood vessels it can travel to various organs and block blood vessels in the heart, lungs, or brain which can cause stroke and even lead to death.

Treprostinil Injection is formulated for subcutaneous or intravenous infusion. The product is a prostacyclin vasodilator indicated for the treatment of pulmonary arterial hypertension to diminish symptoms associated with exercise and for patients who require a transition from epoprostenol to reduce the rate of clinical deterioration.

Treprostinil Injection 20mg/20mL (1mg/mL) is distributed in 20mL multidose vials as sterile solutions in water for injection, individually packaged in cartons under NDC #42023-206-01. Only Lot 57014, expiration date 04/2024 is affected by this recall. Vials from the affected lot bear the attached label.

Par is providing written notification to wholesale accounts and the hospital location that has received the affected lot and is arranging for the return of all existing inventory of Lot 57014 through Inmar, Inc. Wholesale distributors and hospital pharmacies that have the product being recalled should immediately discontinue the use and stop distribution immediately.

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 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: Endo International, Par Pharmaceutical
Brand name: Par Pharmaceutical
Product recalled: Treprostinil 20mg/20mL Injection
Reason for the recall: Potential Presence of Silicone Particulate Matter
FDA Recall date: March 12, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-pharmaceutical-issues-voluntary-nationwide-recall-one-lot-treprostinil-injection-due-potential
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