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Power Outage, Princess Anne Rd & N Landing Rd, Virginia Beach, VA 23453, USA
1 month ago
Virginia Beach, 23453 Virginia, United States
Dominion Energy customers in the North Landing area experienced a power outage that lasted several hours because a vehicle crash resulted in a broken pole, causing the outage. The following intersections were affected: Holland at Nimmo, Holland at Princess Anne, Indian River at West Neck, Indian River at North Landing. As of 6:30 p.m., around 2,500 customers were without power.
Outage link: outagemap.dominionenergy.com
Source: wtkr.com
Published: 2022 04 25
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A line of strong thunderstorms moved through the Charlotte area early Friday, knocking out power for more than 2,000 Duke Energy customers. As of 8:40 a.m., about 1,650 customers were without electricity in north Charlotte, along Statesville Road, from Interstate 485 to about Stumptown Road, according to... See More Duke Energy’s outage map. Nearly 500 along Ardrey Kell Road near Tom Short Road in south Charlotte also are affected. About 300 customers in northwest Charlotte and about 600 in along Unity Church Road on Lake Norman in Denver, N.C., are also without power.
Outage link: outagemaps.duke-energy.com
Source: charlotteobserver.com
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Power Outage, Saginaw Charter Township, MI, USA
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Power Outage, Hoodsport, Washington 98548, USA
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The Mason County public utility district (PUD) said a power outage Friday morning was caused by theft or vandalism on high-voltage lines. At 5:29 a.m. power had been restored in Hoodsport and they were working to restore power from the winery to Tillicum Beach and Galloway Lane... See More in Brinnon.
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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
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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
FDA Recall date: May 06, 2022
Source: fda.gov See Less
Missing/delayed package, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
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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.
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