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Power Outage, Cambria, San Luis Obispo County, CA, USA

2 years ago

Cambria, California, United States

While PG&E shut off the power to 246 customers in San Luis Obispo County because of gusty winds that could increase the risk of wildfires, another 5,196 customers also lost power during Monday’s wind event.

In addition, the lights went out in parts of Cambria for 1,223 PG&E customers at 1:40 p.m.

Shortly after 3 p.m., 410 PG&E customers lost power in rural Santa Margarita.

At 4:35 p.m., 3,531 PG&E customers in parts of Pismo Beach, Grover Beach and Arroyo Grande lost power.

Source: calcoastnews.com/2021/10/5432-customers-without-power-in-san-luis-obispo-county/
Source publication date: 2021 10 11

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More than 10,700 PG&E customers were hit with power outages on Sunday 4th morning in Cambria, Morro Bay, Los Osos, San Luis Obispo, Paso Robles, Arroyo Grande, Templeton and Pismo Beach. The largest outage, 6,695 customers lost power in Los Osos, according to PG&E.

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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.

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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

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