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18 hours ago
Thousands are without power in Virginia due to severe weather. 8,718 Appalachian Power customers in Virginia without power:
Bedford - 1,660
Franklin - 1,013
Montgomery County - 764
Buchanan - 604
Wythe - 488
Roanoke County - 203
Floyd - 95
Henry - 87
Giles - 76... Roanoke City - 37
Galax - 24
Grayson - 15
Carroll - 15
Pulaski - 9
Patrick - 5
Bland - Less than 5
Lynchburg - Less than 5
Outage link: outagemap.appalachianpower.com.s3.amazonaws.com
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... 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
Outage link: outagemaps.duke-energy.com
15 hours ago
Nearly 6,500 Consumers Energy customers in Saginaw County lost power Friday morning. The outage was reported at 10:51 a.m.
Outage link: consumersenergy.com
11 hours ago
More than 2,000 Westmoreland County homes and businesses are currently without power. Approximately 33% of Northern Neck Electric Cooperative customers have been affected.
Outage link: nnec.ebill.coop
11 hours ago
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... in Brinnon.
Outage link: scripts.masonpud3.org
The boil order put in place for Weir Avenue Wednesday has been lifted, according to the Weirton Area Water Board.
Weir Avenue, from Lee Avenue to Pennsylvania Avenue, is under a boil order following work on a water line today.
Recent Interesting Reports
St. Paul, Minnesota, Fagron Inc. (“Fagron”) is voluntarily recalling two lots of SyrSpend SF Cherry to the hospital, pharmacy, and distributor level out of an abundance of caution. The affected lots are potentially contaminated with Burkholderia gladioli.
Burkholderia gladioli is an opportunistic pathogen most commonly affecting patients... with respiratory disease. Patients with compromised immune systems such as those with Cystic Fibrosis are at higher risk. Burkholderia gladioli also can cause complications after transplants. Exposure to contaminated product could lead to adverse events, which could be severe for at-risk individuals.
Fagron has received three complaints regarding an undesirable smell associated with the product. To date, Fagron has not received any reports of adverse events related to the product being recalled. Fagron sells this product for the extemporaneous compounding of prescriptions for oral dosing. The affected lots with expiration dates are listed below.
Item number: 805359
Size: 500 mL
NDC number: 51552-1123-5
Expiration date: 08/31/2024
Item number: 802496
Size: 4 L
Expiration date: 08/31/2024
Fagron has already notified its distributors and customers by phone, e-mail, and/or letter and is arranging for return of all recalled products. Hospitals, pharmacies, and distributors that possess affected product should quarantine this material and await further instructions from Fagron or Fagron’s recall coordinator. Please immediately discontinue use or distribution of the recalled product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Company name: Fagron Inc.
Brand name: Fagron
Product recalled: SyrSpend SF 500mL and 4L
Reason of the recall: Potential contamination with Burkholderia gladioli
FDA Recall date: May 02, 2022
Heartland farms about dog food I purchased. I bought the big bag of heartland farms dog food yesterday and tonight my dogs got sick and got diarrhea | Symptoms: Diarrhea
Driver completely destroyed my yard as well as my cement planter that is my property marker. They decided to use my yard as a short cut through to the main road. They took out my cement planter in the process. It had a flagged reflector so there... was absolutely no reason they could of not seen it there. When approaching the van, they decided to hop back into the van and sped off while destroying my yard in the process. They endangered my mothers safety when she went to approach the situation. Their reckless driving is a safety concern and could of caused my mother bodily harm
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... 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
FDA Recall date: May 06, 2022
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... lots are impacted.
The recalled product is:
Anagrelide Capsules, USP 0.5 mg
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
Brand name: Teva
Product recalled: Anagrelide Capsules
Reason of the recall: Dissolution Test Failure
FDA Recall date: May 23, 2022
2 weeks ago
I just opened My package and the sunglasses are in many pieces broken and I wanted to wear them next week on My trip to Annapolis to see My Granddaughter Graduate the Naval Academy
It's a sexual supplement, called Captain Boss Bully Ruby 10000. My wife and I both took one each. We both started shaking horribly uncontrollably, our heads started throbbing, and we started sweating profusely. I started throwing up she didn't. Both of us had problems with our eyes.... Eyes were bloodshot red and super glassy. Don't know what's in those but it's nothing like the pink pussycat pill or the Rhino pills. | Symptoms: Nausea, Vomiting, Sweating, Shaking
Last 30 days