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Power Outage, La Cadena Ave & West Huntington Drive, Arcadia, CA 91007, USA

11 months ago

Arcadia, 91007 California, United States

Electrical fire causes power outage at Santa Anita Mall in Arcadia. Traffic lights in the area were also impacted, leaving shoppers and diners who had to evacuate caught in major traffic jams.

Outage link: sce.com
Source: news.yahoo.com
Published: 2023-03-25

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The City of Frederick is preparing for an schedule power outage to repair a substation. It’s going to last about 12 tonight March 19th, until about 6 o’clock in the morning.

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Multiple power outages Monday morning affected more than 1,500 Duke Energy customers. The outages were spanned to West Lafayette in the area of State Street and River Road, according to Duke's online power outage map. The outages were caused by a vehicle damaging Duke's equipment. Power has... See More been restored to the area.

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A power outage was reported in Fort Wayne, after a car crash due to exceeding the speed limit. According to the Police, the SUV crashed through a fence and into a utility pole, causing a fire and a power outage in the area of Lower Huntington Road.... See More Power has been restored to the area.

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A power outage has been reported in Honeydew today March 18 at 11:11 a.m. Customers affected: 114. Cause of the outage: Planned Shutdown. The estimated restoration time is today, March 18 at 4:00 p.m.

Outage link: pgealerts.alerts.pge.com
Source: lostcoastoutpost.com
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I received a package with a small strawberry tag in it i did not order. I want my full refund from Lisa Holland at 11819 Goldring Rd Arcadia, CA 91006 I did order some Christmas items not a strawberry tag with a gold ring to attach it to something who knows what. See Less
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A pair of sunglasses that I did not order.
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Arcadia, Ca 91006
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I received a small package from Lisa Holland in Arcadia California and it’s a case with sunglasses. I do not wear sunglasses so I would not have ordered these. I have the protector built into my eyeglasses. I have no idea how they got my information.

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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: fda.gov
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