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Boil Water Advisory, Breckenridge, Texas, USA

2 years ago

Breckenridge, 76424 Texas, United States

A boil water notice has been issued for all City of Breckenridge water customers.

Source: ktxs.com/news/local/boil-water-notice-issued-for-the-city-of-breckenridge-water-customers
Source publication date: 2021 09 29

1


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A precautionary boil water advisory has been issued for customers who get drinking water from the Runnelstown Utility District, located in Perry County. The notice will affect customers on Hinton Loop, Conway Road, and Pumping Station Road.

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The Walnut Bayou Water System issued a boil advisory on March 28, 2024, for areas in Tallulah, La., effective immediately. The affected areas are 772 – 2260 Hwy 80 West, 335 Gregory Rd, Butts Dr, 126 Cox Rd, 149 Hilderbrand Rd, Eldorado Plantation Dr, Averett Rd, 317... See More Fred Morgan Rd, 123 Lance Morgan Rd, Quebec Rd, 108 – 377 West Bear Lake Rd, Bedgood Rd.

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Residents of Fore Acres, Hillside Acres and Courtney Acres should boil water they use for drinking, cooking, and brushing teeth, Marion County Utilities announced Wednesday 27th. The public utility issued a precautionary boil water notice Wednesday because of a water main repair.

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Comfy Platform shoes is a rip off I ordered UGGS BOSTON SLIPPERS FOR MEN received a knock off that fits a woman 8.5
The only phone number I can find ONLINE for: COMFY PLATFORM SHOES doesn’t work to contact seller. I ordered The brand : UGGS style... See More BOSTON SLIPPERS for men Size 9 in men’s (I’live on disability my grandson is Freshman in highschool this was his Christmas Present See Less
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The City of Breckenridge has declared a Boil Water Notice effective Wednesday, March 1, 2023, for several blocks in the north-central portion of the city. The notice is for the area from North Rose Avenue to North Parks Street and from West Second Street to West Lindsey... See More Street, including Breckenridge High School and Junior High.

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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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