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Power Outage, East Killarney Circle, Wichita, KS, USA

4 weeks ago

East Killarney Circle, Wichita, 67206 Kansas, United States

Power out a few minutes ago.

279


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Nearly 4,000 Evergy customers are without power on this hot and muggy afternoon. According to the energy provider’s outage map, one area impacted runs from 13th Street N. to 25th Street N. and from Amidon to I-135. The other is located in the Schweiter neighborhood, between Lincoln... See More and Harry, from I-135 to George Washington Boulevard.

Outage link: outagemap.evergy.com
Source: kwch.com
Published: 2022-05-09
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Tornado has ripped through parts of Sedgwick and Butler Counties on Friday evening, leaving hundreds of people without power. Evergy’s website reports that 23,098 customers are without power, with 336 total outages.

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Safely Power Outage AD
The Kansas Department of Health and Environment (KDHE) has issued a boil water advisory for the Eberly Farms, Inc. public water supply system located in Sedgwick County. This advisory is not related to COVID-19.

Source: kwch.com
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The Kansas Department of Health and Environment (KDHE) has issued a boil water advisory for the Eberly Farms, Inc. public water supply system located in Sedgwick County.

Source: twitter.com
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On December 2nd a team lead came to me and told me to fill out the covid vaccine status form. When the device I was filling it out on crashed multiple times, the team lead told me to just falsify my response instead of finding a way... See More to fill out the form honestly. There was one other employee present, but I feel that this action put the entire store at risk.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2022-01-10
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1. Multiple known COVID positive employees being allowed to work in building in close proximity to others. Some are symptomatic. Protection like masking is being left up to the employees who are positive, so a number of them are walking around without any protection at all. 2.... See More The COVID positive employees are being allowed to continue working in building, without masks or any other protection methods


Source: Osha.gov | Receipt Date: 2022-01-26
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A power outage on the westside plunged thousands of Wichitans into the dark around 10:15 Sunday morning. The outage closed several businesses in the New Market Square area, like the Dillons at 21st and Maize, for a couple of hours. A problem at a substation caused the... See More outage that affected about 2,700 customers.

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Location is in the paint booths: 1. Supplied airhood used, fresh air has stopped flowing and employee(s) have difficulties to breathe. 2. Not performing blood testing for hexavalent chromium. 3. No fit- testing for respirator use nor medical surveillance. 4. Chromium out all over the floor. 4.... See More Employees exposed to cuts: Razor blades everywhere. 5. Not testing air quality to verify safe use. Supplied air unit has never tested, maintained. 6. Employees exposed to chemicals; it smells.] 7. No training on Hazard Communication. 7. Training on respirator use has never been given. 8. Poor housekeeping practices. No sanitation cleaning products to use for removing paint and stuff from hands etc. 9. Employees not using PPE properly, or at all. No training on PPE use. Employees painting with their hoods off. 10. No vacuum system. 11. Painters are changing filters with no HAZMAT certification. 12. Covid-19 incidents is not being reported.

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A boil water advisory has been issued for the City of McFarland in Wabaunsee County by the Kansas Department of Health and Environment on Wednesday. The KDHE is advising local residents of McFarland that the public water supply system is now in a boil water advisory.

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The OMMA alerted growers and processors about the recall and they are required to inform dispensaries, who will inform the patients who purchased the product. Any patient in possession of a recalled product should return it to the dispensary.

In case you experience harm from marijuana 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. If symptoms persist, seek medical care.

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Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary recall was initiated due to dissolution test failure detected during routine stability testing. No other... See More lots are impacted.

The recalled product is:
Anagrelide Capsules, USP 0.5 mg
NDC: 0172-5241-60
Lot # GD01090
Exp. Date 05/2022

Administration of this product with lower dissolution – taking longer to dissolve once ingested -- may result in decreased effectiveness or ineffectiveness of the drug to exert its platelet-reducing effect. Failed dissolution can result in a slower rate and extent of drug release leading to less anagrelide available in the body. For seriously ill patients with elevated platelet counts, less available anagrelide in the body could increase the risk of clotting (blood coagulation), and clotting or bleeding events such as a heart attack or stroke, which could be life-threatening. To date, Teva has not received any product quality complaints or adverse event reports, of this nature, for the recalled lot.

Anagrelide capsules are indicated for the treatment of patients with thrombocythemia, secondary to myeloproliferative neoplasms, to reduce the elevated platelet count and the risk of thrombosis and to ameliorate associated symptoms including thrombo-hemorrhagic events. Information about the affected lot is listed in the table below. It is packed in bottles with 100 Capsules. Teva distributed 4224 bottles nationwide from 07-30-2020 through 09-02-2020 to its wholesale, distributor and retail customers under the label for Teva Pharmaceuticals USA, Inc.

Company name: Teva Pharmaceuticals USA
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Product recalled: Anagrelide Capsules
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Natural Organics, Inc., is voluntarily recalling four lots of NaturesPlus Keto Living Sugar Control Capsules 90 count, because it was found to contain gluten. People who have allergies to wheat or gluten run the risk of serious or life-threatening allergic reactions if they consume these products. There... See More have been no reported incidents of illness or adverse reactions in connection with these products to date.

Individuals with Gluten intolerance may experience minor to severe reactions after consuming this product. This could include upset stomach, diarrhea, fatigue, skin reactions and more. It was discovered during routine testing that the product contains gluten. It was subsequently discovered that a raw material that is normally gluten free tested positive for gluten.

Gluten is a general name for the proteins found in wheat (wheatberries, durum, emmer, semolina, spelt, farina, farro, graham, KAMUT® khorasan wheat and einkorn), rye, barley, and triticale – a cross between wheat and rye.

The listed products were distributed nationwide to consumers, retail stores and to the following foreign countries: Kenya, Spain, Trinidad, United Arab Emirates, and the United Kingdom. The capsules are packaged in white jars and black caps; with labels having orange, white and black print bearing the product codes, lot numbers and “Best By” or “BBE” (Best Before End) dates are printed on the bottom of the bottle.

The lots affected are:

- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. 82004, UPC Code 097467820043, Lots 1362073, Best By 10/2025 and 1365200, Best By 10/2025
- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. Ue82004, UPC Code 097467820043, Lots 1361754, BBE 10/2025 and 1364325, BBE 10/2025

Consumers who may have purchased affected lots of NaturesPlus Keto Living Sugar Control Capsules are advised to return them to the place of purchase. No other Natural Organics, Inc. products are affected by this recall. Natural Organics, Inc. has removed all affected products within existing inventory.

This voluntary recall is announced in accord with FDA guidelines. We are initiating recall notices to our accounts and consumers who received inventory of the recalled products with instructions for returning the recalled products and for notifying their customers of the recall. Consumers with questions may contact the company Monday – Friday, from 8:00 am to 4:30pm EDT.

Company name: NATURAL ORGANICS, INC
Brand name: NaturesPlus
Product recalled: Keto Living Sugar Control Capsules
Reason of the recall: Undeclared Gluten
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Source: fda.gov
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