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A Boil Water Notice is in effect for all Lexington Water Customers.
Source: cityoflexingtontx.com
Published: 2023-02-02
3
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According to city officials in Escanaba, a boil water advisory has been issued due to construction. Affected areas include 600, 700, and 800 blocks of 20th Street. 600, 700, 800, 900, 1000, 1100, 1200 blocks of 19th Street. 1,800 and 1,900 blocks of 6th Avenue S. 1,900,... See More 2000, 2,100 blocks of 8th Avenue S. 1,800 blocks of 10th Avenue S, and 1,100 S South Street.
Source: uppermichiganssource.com
Published: 2024-03-27 See Less
8
The City of Centralia has issued a boil order for residents on North Pine Street from Broadway to McCord.
Source: southernillinoisnow.com
Published: 2024-03-27 See Less
13
On Wednesday, March 27, 2024, there will be a water outage until 3:00 p.m. in the areas of Government Avenue from Clark Avenue to Holcomb Boulevard, including Bills Avenue South to Stuart Avenue. This will also include Holcomb Boulevard from Ogden Avenue going North to the railroad... See More tracks, including Bradford Circle. The purpose of this water outage is to repair a hydrant. After repairs, a boil water advisory will be in place.
Source: wxxv25.com
Published: 2024-03-27 See Less
27
Boil Water Advisory, Hope Drive, Fremont, IN, USA
10 hours ago
Portions of Fremont are under a boil advisory for water after a water main break occurred on Wednesday morning. Customers under the boil advisory are those who live in the Nicholas Trail, Rachel Lane, Hope Drive, and Springhill Court areas of the town’s north end, near Fremont... See More Community Church. The break occurred near Nicholas Trail and Rachel Lane.
Source: kpcnews.com
Published: 2024-03-27 See Less
10
Boil Water Advisory, County Road 2118, Rusk, TX, USA
10 hours ago
Due to a water main line leak, the Texas Commission on Environmental Quality has required the Rusk Rural Water Supply Company PWS# 03 70054, public water system to notify all customers to boil their water before consumption. The affected areas include FM 1248 (not all of FM... See More 1248-lf correct number is on account customer will receive a call) County Roads: 2107,2109,2110,2111,2115,2117,2118,2119,2120,2121.
Source: thecherokeean.com
Published: 2024-03-27 See Less
7
I received a product that I did not order. It's a sugar product, for energy , idk , called VERTI Biorbose
From Humble House , the address on the package was ,
Fullfillment House
Po box 5708
Tampa FL. 33675 - 5708
It cane with a clear... See More wrapping, no instructions, couldn't even read what was on the container See Less
239
Power Outage, Fayette County, KY, USA
3 weeks ago
Thousands in Kentucky are without power after a widespread line of severe storms and tornado watches impacted the state Wednesday 28 morning. There are 335 customers without power in Fayette County, according to LG&E & KU’s power outage map.
Outage link: lge-ku.com
Source: kentucky.com
Published: 2024-02-28 See Less
238
Received a pair of cheaply made denim jeans which were not ordered. See Less
238
Power Outage, Paris Pike, Lexington, KY, USA
2 months ago
An equipment failure at a Kentucky Utilities (KU) substation on Paris Pike left 1,200 customers in Scott County without power on Sunday morning Jan 21. The power outage began at 6:55 a.m. and lasted until 9:20 a.m. after a breaker malfunctioned.
Outage link: stormcenter.lge-ku.com
Source: news-graphic.com
Published:... See More 2024-01-22 See Less
238
I received a package with a doll house book shelf in it and i did not oder and do not know how they got my address 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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