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Boil Water Advisory Lifted, Barnesville, OH, USA

2 years ago

Barnesville, 43713 Ohio, United States

The Barnesville Water Department has lifted the precautionary boil advisory due to emergency waterline repairs for all service connections on Hunts Avenue, Carrie Avenue, South Highland Avenue, Hilles Avenue, and Dewey Avenue, and any others experiencing a loss in pressure.

Source: twitter.com
Published: 2022 01 17

16


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The Barnesville Water Department issued a precautionary boil advisory on Wednesday morning 27th due to waterline repairs for all service connections on East Main Street between Henderson Street and Warren Avenue and any other locations experiencing a loss in pressure.

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A boil water order has been issued for some areas in Barnesville. According to The Barnesville Water Department, a main water valve will be replaced on Cherry Street. The affected area is Cherry Street and North Arch Street from East Walnut Street to the dead end. The... See More boil advisory will be in place for 48 hours once water service is restored.

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The Barnesville Water Department has issued a precautionary 48 hour boil advisory due to emergency waterline repairs for all service connections on South Chestnut Street from Main Street to South Street, and any others experiencing a loss in pressure.

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I purchases a cordless lawn trimmer paid 38.90 plus tax was charge to my credit card and never received, Bye a cordless Lawn Trimmer on July 9 2023 and never received and my credit card was charge 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
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