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Oroville East, California, United States
Updated: September 14, 2022 11:24 AM
More than 1,600 PG&E customers were without power in the Oroville area, according to the PG&E outage. Just after 11 a.m., the power was restored. At about 7:39 a.m., 1,656 customers lost power along Highway 162. Customers who live near Lincoln Street and Oroville Dam Boulevard were... without power. Some customers who live off Oroville Quincy Highway in Brush Creek and the Berry Creek area were also without power. PG&E said the outage was caused by a guy wire that became wrapped around a power line. Guy wires are support cables that attach to the top of the pole to the ground at an angle to help support the pole. PG&E said a vehicle collided with the guy wire at Olive Highway and Arbol Avenue. Power is estimated to be restored at 11:45 a.m.
Outage link: pgealerts.alerts.pge.com
According to PG&E's Outage Map, 1,534 customers were without power in the Oroville East area.
Outage link: pgealerts.alerts.pge.com
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AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), contains acyclovir, a synthetic nucleoside analog, active against herpes viruses. Acyclovir Sodium Injection is indicated for the treatment of initial and recurrent mucosal and cutaneous herpes simplex (HSV- 1 and HSV-2) in immunocompromised patients and initial clinical episodes of herpes genitalis in immuno-competent patients. It is packaged in a glass vial labeled with NDC 55150-154-10. The lot being recalled is AC22006 with an expiration date of 08/2023. Eugia US LLC shipped the entire lot to wholesalers nationwide from June 8, 2022, through June 13, 2022.
The product label is as shown below: Eugia US LLC is notifying its direct consignees by recall letters and is arranging for return/ replacement of all recalled products. Wholesale customers and health professionals that have the product lot which is being recalled should immediately place the recalled lot on hold.
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. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experienced 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.
Company name: Eugia US LLC
Brand name: Auromedics
Product recalled: Acyclovir Intravenous Product
Reason of the recall: Presence of a dark red, brown and black particulate inside the vial
FDA Recall date: September 27, 2022
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