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Power outage, Terre Haute, IN 47802, USA

2 weeks ago

Terre Haute, 47802 Indiana, United States

Out as of 17:15, 7/24/2022

128


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According to the Hawaiian Electric Company, over a thousand customers are without power in the Kalihi area. On Wednesday, Aug. 10 around 4:30 p.m. customers lost power, reported HECO. Cities affected are Iwilei, Kalihi, Kalihi Valley, Kapalama, Liliha and Palama.

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According to Overton Power District No. 5, a fire affecting the 230KV transmission power line has caused a system-wide power outage that is affecting Mesquite, Bunkerville, Logandale, Moapa and Overton, Nevada.The outage also includes Lincoln County (Panaca, Pioche, Alamo, Caliente), and Scenic, Arizona.

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According to Overton Power District No. 5, a fire affecting the 230KV transmission power line has caused a system-wide power outage that is affecting Mesquite, Bunkerville, Logandale, Moapa and Overton, Nevada.The outage also includes Lincoln County (Panaca, Pioche, Alamo, Caliente), and Scenic, Arizona.

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According to Overton Power District No. 5, a fire affecting the 230KV transmission power line has caused a system-wide power outage that is affecting Mesquite, Bunkerville, Logandale, Moapa and Overton, Nevada.The outage also includes Lincoln County (Panaca, Pioche, Alamo, Caliente), and Scenic, Arizona.

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According to Overton Power District No. 5, a fire affecting the 230KV transmission power line has caused a system-wide power outage that is affecting Mesquite, Bunkerville, Logandale, Moapa and Overton, Nevada.The outage also includes Lincoln County (Panaca, Pioche, Alamo, Caliente), and Scenic, Arizona.

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According to Overton Power District No. 5, a fire affecting the 230KV transmission power line has caused a system-wide power outage that is affecting Mesquite, Bunkerville, Logandale, Moapa and Overton, Nevada.The outage also includes Lincoln County (Panaca, Pioche, Alamo, Caliente), and Scenic, Arizona.

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According to Overton Power District No. 5, a fire affecting the 230KV transmission power line has caused a system-wide power outage that is affecting Mesquite, Bunkerville, Logandale, Moapa and Overton, Nevada.The outage also includes Lincoln County (Panaca, Pioche, Alamo, Caliente), and Scenic, Arizona.

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A power outage Thursday morning, affecting over 1,500 customers in College Station along Harvey Mitchell Parkway, Texas Avenue, Rock Prairie Road and Welsh Avenue. A cause for the outage has not been determined yet, but crews responded quickly.

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Source: kbtx.com
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Recent Interesting Reports

Alberta Health Services (AHS) is investigating an outbreak of Salmonella infections across the province linked to reptiles and feeder rodents. As of July 22, 2022 , a total of 12 cases have been identified in 4 of 5 AHS Zones (North, Edmonton, Central, and Calgary). Investigation findings... See More have identified exposure to both snakes and feeder rodents (used as reptile food) as a likely source of the outbreak. Investigation into the facilities carrying feeder rodents is still ongoing.

Even if snakes and rodents appear to be healthy, clean and show no signs of illness, they can still carry Salmonella bacteria. Having indirect contact by touching their environments can put you at risk for developing a Salmonella infection.

To prevent direct or indirect spread of Salmonella to yourself or others, AHS advises following these simple steps to help reduce your risk of becoming ill from contact with reptiles (including snakes), rodents and their environments:

- Always wash your hands immediately after touching a reptile or rodent, and anything they eat, or after being in the area where they live, play or touch.
- Regularly clean with soapy water followed by a household disinfectant any surfaces or objects your reptile or rodent touches.
- Never kiss a pet rodent or reptile.
- Reptiles or rodents in homes, daycare centres, schools or other facilities with children aged 5 years and under is not recommended.
- Always supervise children when they touch or play with reptiles or rodents. Do not let them put reptiles and rodents or their supplies near their face or share their food or drinks with pets. Make sure they thoroughly wash their hands after touching reptiles or rodents.
- Do not clean or bathe reptiles and rodents in the kitchen sink or in bathroom sinks or bathtubs.
- Keep reptiles and rodents and all their food, containers and toys away from the kitchen and other places where food is made or eaten.
- Do not keep frozen feeder rodents in the same fridge or freezer as human food. Freezing rodents does not kill Salmonella.
- Always defrost and prepare frozen feeder rodents outside the kitchen, using dedicated utensils and containers.
- Be aware of the specific needs of your reptile. Stress for a reptile can increase shedding of Salmonella.
- Always keep reptiles and live rodents in habitats specifically designed for them.
- If you choose to have a reptile or rodent in your home, talk to your health care provider or veterinarian about the right reptile or rodent for your family, especially if your family includes children, pregnant women, immunocompromised individuals, or adults 65 years of age and over.

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.

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This product was found to contain the undeclared active pharmaceutical ingredient tadalafil. Tadalafil, which is a phosphodiesterase type-5 (PDE-5) inhibitor, is the active ingredient in an FDA-approved prescription drug, used to treat erectile dysfunction (ED). Product was sold through our website, wholesaleonline1.com Mar 2022 to July 2022... See More and ­ distributed in any US State. To date, wholesaleonline1.comhas not received any reports of adverse events related to this recall.

The product comes in a black box and contains 12 sachets of 15 grams of honey with different expiration dates stamped on the back side. This undeclared ingredient (tadalafil) may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to dangerous levels. Men with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.

The recall was initiated after FDA laboratory analysis confirmed that Dose Vital VIP Vital Honey contains the undeclared active pharmaceutical ingredient Tadalafil. Consumers who have purchased Vital Honey on wholesaleonline1.com are urged to immediately discontinue use and return the recalled product for a full refund.

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: MKS Enterprise LLC
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Well we got the treats and my dogs had diarrhea and vomiting and they won’t stop | Symptoms: Diarrhea, Vomiting See Less
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Dream bones killed my 11 yr old dog yesterday! Rubie was my life & loved her so much. I gave these bones to her because she loved them & they caused a blockage & perforated her bowel which she became septic & died within 2days. I plan... See More on destroying every dream bones bag I see in the stores until they stop selling them. I can only hope by doin this it might save atleast one dogs life. SAVE A DOG & DESTROY THESE BONES!! See Less
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Vi-Jon, LLC is revising a previously reported list of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry that were voluntarily recalled to the consumer level to include product that was distributed in the United States, Canada and Panama. This includes all lots of Cherry... See More Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution, 10 FL OZ (296 mL) within expiry. To date, Vi-Jon, LLC is aware of 3 (three) reports of serious adverse reactions potentially related to this recall. Vi-Jon, LLC is in the process of investigating these reports.

On July 14, 2022, Vi-Jon, LLC recalled all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry. The recall was initiated after Vi-Jon, LLCs third party microbial testing identified the presence of Gluconacetobacter liquefaciens.

Risk Statement: Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences. The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle. In addition to the lemon flavor, the recall includes the Cherry flavor and Grape flavor.

On August 3, 2022, the Recall product list has been updated to include the products noted below.

CANADA Equate Canada 300 mL Lemon Magnesium Citrate
NPN # NPN 80015316
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CANADA Life 300 mL Lemon Magnesium Citrat
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CANADA Life 300 mL Cherry Magnesium Citrate
NPN # NPN 80015316
UPC # 057800856405

CANADA Personnelle 300 mL Lemon Citrate
NPN # NPN 80015316
UPC # 055989029306

PANAMA CRUZ BLANC 10OZ LEMON MAG CIT
NPN # N/A
UPC # 308697403082

The product was distributed in the United States, Canada and Panama to wholesale and retail outlets. Vi-Jon, LLC is continuing their investigation into the cause of the problem.

Vi-Jon, LLC is notifying its customers by phone and email and is arranging for return or destruction of all recalled product. Consumers that have this recalled product should stop using and return any remaining product to the place of purchase.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

In case you experienced harm from these products, 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: Vi-Jon, LLC
Brand name: Multiple brand names
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Reason of the recall: Microbial contamination with Gluconacetobacter liquefaciens
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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

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The Parks & Recreation Department has been testing the water at Cascade Lake and the bacteria levels were elevated. The specific bacteria that was showing elevation was E. Coli. Excessive rainfall, extreme heat in shallow bodies of water, which Cascade Lake is relatively shallow, and wildlife can... See More all be common causes for bacteria levels to increase. Parks & Recreation has voluntarily closed the beach until test results return to an acceptable level.

In case you are experiencing E. coli symptoms such as watery diarrhea (often bloody), vomiting; stomach cramps; and mild 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: rochestermn.gov
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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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458


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