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Power outage, Roigan Terrace, Monona, WI, USA

2 months ago

Roigan Terrace, Monona, 53716 Wisconsin, United States

From storm

347


Related Reports

PSO showed around 265 customers initially lost power. Wayne Green with PSO says a bad transformer is to blame.

Outage link: outagemap.psoklahoma.com.s3.amazonaws.com
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An ongoing wildfire burning near Springville has prompted some road closures, evacuation orders and power outages. The power outage is affecting those above Camp Nelson from Rio Vista to Ponderosa.

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The CHP incident website states the fire was reported around 2:30 p.m. on Monday and was located “next to powerline.” Doyle Springs, Camp Nelson, Pierpoint and Ponderosa are also without power at this time.

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Duke Energy is reporting more than 2,500 people are without power Monday evening. At this time, Duke Energy is reporting the cause as unknown.

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Hundreds are without power in Pembroke after a car ran into a couple power poles on 119, according to Pembroke Police. The north side of the city is without power, including schools in the area.

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A planned power outage is scheduled for Thursday night and will impact a few Springfield streets, Ohio Edison announced. The outage is expected to begin around 9-9:30 p.m. and will last for approximately 60 minutes as crews work to repair a substation in the area. Impacted streets... See More include West Rose Street north to the railroad tracks at West High Street, between Dayton Avenue and Yellow Springs Street; and, West Rose Street south to Leffel Lane, between South Yellow Springs Street and Center Boulevard, according to City of Springfield social media post. 2200 residential and commercial customers will be affected.

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Source: springfieldnewssun.com
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According to the BWL outage map, there were three active outages as of 5:30 a.m. Tuesday, with 1,865 customers in the area south of I-496 along South Waverly Road, and stopping north of West Jolly Road. Other areas of the map show an equipment failure along the... See More Grand River, across from Moores Park as well as equipment failure on Moores River Drive near Frances Park. The cause of the third outage is currently unknown.

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A tree down in the road is causing power problems for hundreds of people in Lexington. Russell Cave Road at Dixiana Domino Road is shutdown due to a downed tree and power lines. It’s the result of an earlier crash. Kentucky Utilities estimates more than 300 people... See More without power.

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NorthWestern Energy is planning a power outage affecting customers on the east side of Hauser Lake on Aug. 16. From 8 a.m. to 4 p.m. on Tuesday, NorthWestern Energy customers in the American Bar, Nelson and Eldorado areas will be without power.

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Recent Interesting Reports

The FDA is cautioning pet owners not to feed their pets certain lots of Darwin’s Natural Pet Products raw cat food after samples from these lots tested positive for Salmonella, and they represent a serious threat to human and animal health. These products are manufactured by Arrow... See More Reliance Inc., doing business as Darwin’s Natural Pet Products, and are sold online direct to consumers. These foods have been associated with cases of illness in three kittens in a single household.

The FDA recommended that Arrow Reliance Inc. voluntarily recall these products and notify the public, but the company has not done so.

The affected products are:
- Darwin’s Natural Pet Products Natural Selections Antibiotic & Grain Free Chicken Recipe for Cats, Lot 9116, manufactured on May 2, 2022.
- Darwin’s Natural Pet Products Natural Selections Antibiotic & Grain Free Turkey Recipe for Cats, Lot 9121, manufactured on May 4, 2022.

The products are sold in white and clear plastic packages with blue and green labeling. Each pack weighs two pounds and consists of four separate units. The lot codes are on the front lower left unit of the package.

If you have these lots of Darwin’s Natural Pet Food, or you can’t be sure of the lot code of the products you have, throw them away. Do not feed them to your pets.

Pet foods contaminated with Salmonella are of particular public health importance because they can affect both human and animal health. Pets can get sick from Salmonella and may also be carriers of the bacteria and pass it on to their human companions without appearing to be ill. People who think their pets have become ill after consuming contaminated pet food should first contact their veterinarians.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: fda.gov
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459


I am a resident of 817 Rose Lane and over a period of nearly 4 weeks I’ve reported a dead branch on a tree on the parkway hanging over my driveway and street. It nearly scrapes the top of my car and my lawncare people have to... See More duck the branch to cut my grass. This is dangerous and I have had no active response from public works. Spoke to someone from public works and city hall with no results 3 times. See Less
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The CFIA announced the recall of raw frozen Primal Patties for Dogs Beef Formula because it may be contaminated with Listeria monocytogenes, posing a risk of cross-contamination and illness after handling the pet food. This product was sold in British Columbia. As of August 2, 2022, the... See More company has not received any reports of incidents or illness in Canada.

The recalled product is:
- Primal Patties – Beef Formula, 6 lb, Case UPC: 854495006173, Unit UPC: 850334004164, Lot code number: W10068709, Best by date: 05/22/23.

The lot code number and best by date can be found on the back of the product packaging above the Primal Pet Foods Inc. red oval logo. Only lot code number W10068709 is included is this recall.

Animals that become infected with Listeria monocytogenes could display symptoms similar to humans. Listeria monocytogenes can affect animals eating the product, and there is risk to humans from handling the products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to the products.

Consumers should immediately stop using the recalled product and dispose of the product.

In case you are experiencing Listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care. If symptoms persist, seek medical care.

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That Bay Area Homeless Shelter Is A Horrible Place And They Letting My Partner Be Out On The Street Homeless To Purposely Separate Us While I'm 5 Months Pregnant Going Through A Lot Of Pain Here By Myself
My Partner Ran Out Of Gas On July 13th... See More And Couldn't Make It Back Here Before Curfew Time At 10pm I Was Worried And Didn't Know What He Was Going Through Until The Next Morning Because His Phone Isn't On He Had No Way To Contact Me Or The Shelter He Begged His Mom For A Few Bucks And Made It Back The Morning If July 14th And This Shelter Gave Him No Chance Told Him He Had To Leave That's No Way To Be Treating People We Both Have Tried Numerous Of Times To See If They Would Let Him Back And They Literally Are Keeping Us Separated On Purpose It Seems Because Neither Of Us Have Done Anything Wrong For Him To Be Out On The Streets Like This While I'm Here Alone 5 Months Pregnant See Less
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The Washtenaw County Health Department and the Washtenaw County Parks and Recreation Commission announced that Independence Lake beach has been closed for swimming the due to high levels of E. coli bacteria. The beach will reopen once follow-up tests confirm levels are low enough to safely swim... See More again.

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DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to the consumer level. FDA analysis has found the product to contain undeclared sildenafil. Sildenafil is a phosphodiesterase (PDE-5) inhibitor found in FDA-approved... See More products for the treatment of male erectile dysfunction. The presence of sildenafil in SANGTER makes it an unapproved new drug for which the safety and efficacy has not been established and, therefore subject to recall. To date, DISTRIBUTOR RFR, LLC. has not received any reports of adverse events related to this recall.

The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in a 7-count blister pack within a carton, UPC 0 705632 523285, and was distributed through retail stores in the state of Florida from 02/01/2002 to 07/20/2022 and Nationwide in the USA through our website from 02/01/2002 to 07/20/2022  www.sangter.com.

Distributor RFR, LLC is notifying its distributors and customers through this notice and is arranging for the return of all recalled products. All customers are urged to stop consuming the product marked with this lot, and to contact their physician or health care provider if they have experienced any problems that may be related to taking or using this medication.

Risk Statement: Use of SANGTER with undeclared sildenafil may pose a threat to consumers because it may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population who are most likely to use these products, adult males who use nitrates for cardiac conditions are at the most at risk from these products.

Company name: Distributor RFR, LLC
Brand name: SANGTER
Product recalled: SANGTER Energy Supplement, 3000mg
Reason of the recall: Undeclared Sildenafil
FDA Recall date: August 02, 2022

Source: fda.gov
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459


Ultra Supplement LLC is voluntarily recalling lot number DAP272109, exp 4/1/26 of Sustango capsules packaged in 10-count blisters packaged in a carton to the consumer level. Ultra Supplement was notified by Amazon that laboratory analysis has found the product to be tainted with tadalafil, an ingredient in... See More FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com nationwide in the USA. To date, Ultra Supplement has not received any reports of adverse events related to this recall.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.

The presence of tadalafil in Sustango makes this product an unapproved drug for which the safety and efficacy has not been established and therefore, subject to recall.

Consumers with underlying medical issues who take Sustango capsules with undeclared tadalafil may experience health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. The product is marketed as a dietary supplement for male enhancement and is packaged in 10-count blisters packaged in a carton, ASIN X0024468I9. The affected cartons include Lot DAP272109, Exp. 4/1/26. The product can be identified by the label below.

Ultra Supplement is notifying its distributors and customers by this press announcement and by Amazon Messaging and is arranging for return of all recalled products. Consumers that have Sustango capsules Lot# DAP272109 should stop using the product.

In case you experienced 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.

Company name: Ultra Supplement LLC
Brand name: Sustango
Product recalled: Dietary Supplement for Male Enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 25, 2022

Source: fda.gov
See Less
459


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