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Boil Water Advisory Lifted, Gerrardstown, WV, USA
10 months ago
Gerrardstown, 25420 West Virginia, United States
Berkeley County PSD has LIFTED the boil water advisory for 91 to 477 Huckleberry Dr., 28 to 209 Myrtle Drive, and 43 to 401 Persimmon Lane in Glenwood Forest Development of Gerrardstown, West Virginia 25420.
Source: twitter.com
Published: 2023-01-17
13
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Berkeley County PSD has LIFTED boil water advisory for Glenwood Lane and Tipperary Trail, all customers located on Tipperary Trail, Sugar Maple Lane, Peanut Trail, Birch Trail and Almond Trail of Glenwood Forest, Gerrardstown, W.V. 25420.
Source: twitter.com
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13
Berkeley County PSD has issued a boil water advisory for the beginning at the intersection of Glenwood Lane and Tipperary Trail, all customers located on Tipperary Trail, Sugar Maple Lane, Peanut Trail, Birch Trail and Almond Trail of Glenwood Forest, Gerrardstown, W.V. 25420.
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Berkeley County PSWD has issued a boil water advisory for the Bentley Drive and Gerrardstown areas.
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Boil Water Advisory, Cove Road, Weirton, WV, USA
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Source: weirtondailytimes.com
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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
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4375 SOUTH LEE STREET
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