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Raleigh County PSD Coal City has LIFTED the boil water advisory for affected customers.
Source: twitter.com
Published: 2022-07-01
36
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The system-wide boil water advisory for customers of the Milton Water and Sewer has been lifted effective 8:58 am March 18, 2024.
Source: 953wiki.com
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The boil water advisory, originally scheduled for March 17, has been canceled, according to DuBois City officials.
Source: gantnews.com
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The Columbia Water laboratory staff has repealed a boil water advisory for customers of Dutch Square Blvd to I-20, Longcreek Rd, Garner Ln, and Diamond Ln, Devonwood Dr, Grays Inn Rd, Wimbeldon Rd, Ashford Ln, Cromwell Manor Dr, Sutton Rd, Chamberlain Dr, Chesterfield Dr, Cambout St, and... See More Riverwind Dr.
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Officials with the Bossier Parish Consolidated Waterworks/Sewerage District No.1 and the Louisiana Department of Health have rescinded the boil advisory issued Wednesday, March 13, for Country Place Subdivision Water System customers.
Source: bossierpress.com
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92
Raleigh County PSD has LIFTED the boil water advisory for the customers of Airport, Arnett, and Coal City.
Source: twitter.com
Published: 2023-03-01 See Less
36
Raleigh County PSD has LIFTED the boil water advisory for the Coal City area.
Source: twitter.com
Published: 2022-08-23 See Less
36
Raleigh County PSD Coal City has LIFTED the boil water advisory for affected customers.
Source: twitter.com
Published: 2022-07-29 See Less
36
Raleigh County PSD has issued a boil water advisory for Independence Road in Coal City.
Source: twitter.com
Published: 2022-07-22 See Less
7
Customers experienced power outages due to a car crash on Athens Road late Wednesday night into Thursday morning, Mar 14 in Princeton. The crash caused the pole to snap in half leaving one part in the road blocking traffic from both ways. Customers in that area lost... See More power throughout the night due to the crash. The broken pole has since been replaced and power is now restored in the area.
Outage link: d2oclp3li76tyy.cloudfront.net
Source: wvnstv.com
Published: 2024-03-14 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
303
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