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Boil Water Advisory, Morrison Rd, Norton, Virginia 24273, USA
2 weeks ago
Morrison Road, Norton, 24273 Virginia, United States
The Wise County Public Service Authority (PSA) has issued a boil water advisory amid waterline repairs on Wednesday. The following areas are under the advisory. Kentucky Ave SE North of Ramsey Road to US58 Bear Creek Road (Norton) Armagosa Road Pendleton Road Wise-Norton Road and adjacent streets Freeman Road Bennett Road Wyatt Road Morrison Road Pine Crest Drive Wayland Drive Industrial Park Road
Source: wjhl.com
Published: 2023-11-15
9
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Officials say due to water main repair that started on December 5, the city of Princeton’s Water Utility is issuing a precautionary boil advisory for its water customers who live north of East Broadway and east of North Race Street.
Source: wwbl.com
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According to the Wise County Public Service Authority, residents are advised to boil water due to an order in effect in parts of Norton Wednesday. The boil water advisory is for the areas of Kentucky Ave SE north of Ramsey Road to US58, Bear Creek Road (Norton),... See More Armagosa Road, Pendleton Road, Wise-Norton Road and adjacent streets including Freeman Road, Bennett Road, Wyatt Road, Morrison Road, Pine Crest Drive, Wayland Drive, and Industrial Park Road.
Source: wcyb.com
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Bushutopia Internet GB Scam, Norton, VA, USA
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Was ordering a fence dog lot got a ugly horse scarf I sent them $40.38 for this fence and got something I didn’t order I want a refund See Less
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Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination, USA
2 weeks ago
Bayer is voluntarily recalling one lot of Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles to the consumer/user level. The product is being recalled due to microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing. It was distributed to wholesale distributors and... See More specialty pharmacies nationwide between January 3, 2023, and February 13, 2023. To date, Bayer has not received any adverse events related to this recall.
Risk Statement: Vitrakvi® is indicated for the treatment of solid tumors that are NTRK gene fusion positive, it is expected that patients on Vitrakvi® may be immunocompromised. Although there is little data in the literature on human pathology caused by Penicillium brevicompactum, there are cases of invasive disease caused by similar Penicillium species, particularly in patients with underlying immunosuppression. Therefore, there is a reasonable probability that ingestion of Penicillium brevicompactum in patients on Vitrakvi® with underlying immunosuppression may result in invasive fungal infections of the blood or pneumonia that can be life-threatening.
The impacted lot of Vitrakvi® is packaged in a 100mL glass bottle with NDC# 50419-392-01 and is identified with Lot# 2114228 and an expiration date of February 29, 2024. Product bottle and carton label images and information on the lot number that falls under this recall is attached
Bayer notified all distributors and pharmacies of this recall on November 8, 2023. Bayer has engaged Qualanex to manage the recall of the product down to the consumer level. Qualanex has notified Vitrakvi® distributors via a recall notification letter and will arrange for the return of the recalled lot from distributors, specialty pharmacies, and consumers.
Consumers who have the recalled Vitrakvi® product should immediately stop use of this particular lot of product and contact their physician or healthcare provider if they have any questions, concerns or have experienced any problems related to Vitrakvi® Oral Solution 20 mg/mL.
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: Bayer
Brand name: Bayer
Product recalled: Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles
Reason of the recall: Microbial contamination identified as Penicillium brevicompactum
FDA Recall date: November 21, 2023
Source: fda.gov See Less
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LUCIA
4375 SOUTH LEE STREET
BUFORD, GA
30518
sent:
Unsolicited package, never ordered a set of two peculiar thin, blue foam 8"x 15" pads w/12 circle cuts on each. Service. #unorderedpackage
#uspostalservice
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