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Boil Water Advisory Lifted, White Sulphur Springs, WV, USA
1 year ago
White Sulphur Springs, 24986 West Virginia, United States
City of White Sulphur Springs has LIFTED the boil water advisory for affected customers.
Source: twitter.com
Published: 2022-05-02
12
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The public works department announced Sunday 24th its boil water advisory — which affected the whole water system — had been lifted. Residents no longer need to boil their water before drinking or cooking.
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A precautionary boil water advisory has been issued for residents living in the White Sulphur Springs area of Greenbrier County. The advisory was originally made on Tuesday, January 16, 2024, due to a water main break in the Route 92 area of White Sulphur Springs.
Source: wvnstv.com ... See More
Published: 2024-01-17 See Less
12
There will be a planned power outage in the White Sulphur Springs area to upgrade equipment. The outage is scheduled for Wednesday, October 25, 2023, from 8:30 a.m. to 2:00 p.m.
Outage link: outages.firstenergycorp.com
Source: wvnstv.com
Published: 2023-10-17 See Less
12
White Sulphur Springs Boil Water Advisory LIFTED in Old White Trail, Villa Ave, Greenbrier Ave,& Park St.
Source: nixle.us
Published: 2023-03-01 See Less
12
White Sulphur Springs Boil Water Advisory effective immediately for Old White Trail, Villa Ave, Greenbrier Ave, and Park St only. Boil all water before consuming.
Source: nixle.us
Published: 2023-02-28 See Less
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City of White Sulphur Spring has LIFTED the boil water advisory for ALL customers.
Source: twitter.com
Published: 2023-01-25 See Less
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Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA... See More SOFT pads were used. These reports of patient burn injuries described up to and including third-degree burns requiring intervention which may lead to prolonged hospital stay, scarring, and additional surgeries in both pediatric and adult patients. Severe burns could lead to potentially long-lasting impacts on patients especially under the age of 12 years.
Since that notification, we have continued to monitor device performance through post market surveillance, investigated every event reported and evaluated potential root cause of these events. Megadyne recently received a report of pediatric use that included a serious 3rd degree patient burn. We are providing this additional broad public communication to increase awareness that MEGADYNE™ MEGA SOFT™ Universal and Universal Plus products should not be used for patients under the age of 12 years.
The list below contains the specific product and codes in scope.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Patient Return Electrode, Product Code: 0845, UDI-DI: 10614559103906.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Dual Patient Return Electrode, Product Code: 0846, UDI-DI: 10614559104248.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Plus Patient Return Electrode, Product Code: 0847, UDI-DI: 10614559104842.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Plus Dual Patient Return Electrode, Product Code: 0848, UDI-DI: 10614559104859.
Customers should review and follow the instructions provided in the December 2023 recall notification (link given below). Mega Soft Universal and Universal Plus Reusable Patient Return Electrodes pads may continue to be used for patients over 12 years of age.
Confirm that personnel using the Mega Soft Universal and Universal Plus pads understand the intended use is changing to patients aged 12 years and older and have stopped using the pads on patients under the age of 12 years. Hospitals using this product should confirm receipt of the recall notification using the business reply form provided with the initial recall notification.
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: Megadyne Medical Products, Inc.
Brand name: Megadyne
Product recalled: Mega Soft Universal and Universal Plus Reusable Patient Return Electrodes
Reason for the recall: Limit use to patients aged 12 years or older.
FDA Recall date: February 29, 2024
Recall link of December 2023: jnjmedtech.com
Source: fda.gov See Less
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