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Boil Water Advisory, Madison St, Fairmont, WV 26554, USA
3 weeks ago
Madison Street, Fairmont, 26554 West Virginia, United States
City of Fairmont Water Dept. has issued a boil water advisory for Madison St and surrounding area.
Sauquoit residents who live on Paris Hill Road from Oneida Street to the Paris Hill tank are under a boil water advisory until further notice.
A boil water notice has been issued for the city of Buffalo Gap. According to city officials, the notice is in effect for the old Aqua Source customers in the Buffalo Gap area until further notice.
The Slate Springs Water Association in Monroe County has issued a Boil Water Notice until further notice for all of its customers.
A boil water notice has been issued by the Arnold Line Water Association. The notice is expected to affect around 330 customers around the Shears Road Apartments, West Lane, North Lane and South Lane; Hillcrest Drive, including the Magnolia Apartments and Weathersby Road from Lowes to the... intersection of Shears Road and Hillcrest Drive.
12 hours ago
Residents in Ridgetop, Tennessee are urged to boil their water due to it potentially being contaminated with fecal coliform or E. coli.
A boil water order was put into effect at 10:30 a.m., Friday, May 27, for the Parthenon Water Association for its customers on Gum Springs Road, Smith Mountain Road, Lone Beech Road and Murray Road. The order is due to tank maintenance work.
Recent Interesting Reports
1 week ago
I have had two packages that have 'gone missing' with USPS and have now had to refund customers. The packages never seem to leave NJ and both contained the same single items (a CD). The first small media mail package was sent on March 15th, 2022 -->... Departed post office in Pitman, NJ on Mar 15 --> arrived at South Jersey NJ Distribution Center March 15 @ 3:54pm --> March 19th - In transit to next facility and no updates after that. During April: spent a few calls completing the 'missing mail' forms both electronically and speaking to 'investigators' who promise to call back. When I receive call-backs it's to say that my missing mail electronic form 'wasn't fully filled out' or that 'the missing report action has not been updated' or that they are 'now pushing it forward.' No notifications from the USPS since then. My second package that I am going to have to refund the customer for was another small media mail package with CD sent April 25th 2022 --> USPS in possession from Sewell NJ --> April 25 2022 Departed Post Office Sewell NJ --> April 29 2022 "In transit, arriving late". It is now May 17th and still no package to the customer.
Something is very wrong with the billing periods as well as the billing, my bill are always through the roof & when I’m paid up they’re always sending outstanding bills & when I call they always claim I’m behind & that isn’t true every month my bill... is over three hundred but my monthly usage is only one hundred so how is this even possible, I need some help here please investigate fairly & truthfully someone, I and the others who are like me thank you so much, no one is above the law & no one should be taken advantage of.
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
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
Medical marijuana products - recalled due to failed tests for mold, E. coli, yeast, and salmonella, Oklahoma, USA
2 days ago
The Oklahoma Medical Marijuana Authority has recalled 99 medical marijuana products after samples failed tests for mold, E. coli, yeast, and salmonella.
During OMMA’s routine inspections and reviewing of records, it discovered results not accurately reported by the testing lab. See images for the list of the... recalled products and Dispensaries.
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.
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
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
4 weeks ago
I ordered something from MI that went to the teterboro distribution center after passing through the metro NY center, which makes no sense since the final destination is in NY. It has been sitting there for 4 days with no movement. I’m getting really nervous about whether... my package will arrive. I need what’s in that box. No response to my inquiries thus far.
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