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Power outage, 148 Signal Hill Dr, St. Louis, MO, USA

2 weeks ago

148 Signal Hill Drive, St. Louis, 63121 Missouri, United States

Power went off at 1:25pm and still off at 4:44 pm. When are you going to turn the power back on in 63121?

859


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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.

Outage link: hawaiianelectric.com
Source: khon2.com
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Route 37 Eastbound apparently has no power from Route 166/Main Street to Vaughn Avenue, with traffic lights out at Peter Avenue, Washington Street, and Vaughn Avenue. Wawas at River Avenue and Hooper Avenue have both gone dark and are closed.

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A transformer fire was in the first block on Ashley Meadows Drive when turning off of Old Tar Road. It appeared the affected areas, in addition to Ashley Meadows, were Main Street Village and Winterfield. Power was out from 6:50 p.m. until 8:10 p.m.

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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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Recent Interesting Reports

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), 100 mL Single Patient Use Glass Fliptop Vial; lot DX9067, to the user level due to a visible particulate observed in a single vial during annual examination of retain... See More samples. The product lot was distributed nationwide to wholesalers/ hospitals/Department of Defense in the United States from June 10, 2020 through June 26, 2020.

The recalled product is:
- Propofol Injectable Emulsion, USP 100 mL Single Patient Use Glass Fliptop Vial, NDC: Vial: 0409-4699-54 Carton: 0409-4699-24, Lot Number: DX9067, Expiration Date Presentation: 01 MAY 2023, Configuration/Count: 1 g/100 mL, Single Patient Use Glass Fliptop Vial Case of 10 Units.

Risk Statement: Patients receiving the impacted product are at risk of experiencing life-threatening adverse clinical effects including but not limited to: blockage of blood vessels, including decreased blood flow to the brain, heart attack, pulmonary embolus, and tissue necrosis. Hypersensitivity reactions and transmission of infectious disease can also occur.

To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for this lot. Propofol is an intravenous general anesthetic and sedation drug for use in the induction and maintenance of anesthesia or sedation. Propofol Injectable Emulsion, USP is a terminally sterilized (TS) product. It is a sterile, nonpyrogenic emulsion containing 10 mg/mL of propofol suitable for intravenous administration supplied in a single patient use fliptop vial.

Wholesalers or hospitals with an existing inventory of the lot, which is being recalled, should stop use and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or hospital level/institution, please notify any accounts or additional locations which may have received the recalled product from you. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.

Company name: Hospira Inc, A Pfizer Company
Brand name: Hospira
Product recalled: Propofol Injection Emulsion, USP
Reason of the recall: Potential presence of visible particulate
FDA Recall date: July 13, 2022

Source: fda.gov
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I ordered 2 Stihl battery operated chainsaws on 7/15/22 order #22071603394 What I received today was 2-10packs of F*CKING tooth brushes from China!!!!!! I called my credit card company and told them about YOUR HUGE SCREW UP and they are looking into IT!! You can refund my... See More $65.12 to my credit card IMMEDIATELY! My package came from 1555 N Chrisman Rd Tracy, CA WHICH is your address.

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Shopaax.com in Newark, DE is voluntarily recalling all lots of Kingdom Honey Royal Honey VIP because it contains undeclared Sildenafil, the active ingredient in the FDA-approved prescription drug Viagra, used to treat erectile dysfunction. FDA approval of Viagra is restricted to use under the supervision of a... See More licensed health care professional. The use of products with the undeclared active ingredient may pose a threat to consumers because the active ingredient 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.

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Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

Company name: Shopaax.com
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Source: fda.gov
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Smyrna, TN, Vi-Jon, LLC is expanding its voluntary recall to include all lots of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry to the consumer level.  This expansion includes all lots of Cherry Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution,... See More 10 FL OZ (296 mL)  within expiry. 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 product was distributed Nationwide to wholesale and retail outlets. To date, Vi-Jon, LLC is aware of 3 (three) reports of serious adverse reactions potentially related to this recall.

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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: Vi-Jon, LLC
Brand name: Multiple Brands
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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.

Source: recalls-rappels.canada.ca
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Niagara Region Public Health's beach monitoring program operates annually from Victoria Day to Labour Day. The goal of is to reduce the risk of illness and injury associated with attending the beach. As of August 04, 2022, the Niagara Region Public Health has flagged 4 beaches as... See More unsafe for swimming.

These beaches are:
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