IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)
Boil Water Advisory Lifted, Benwood, West Virginia, USA
3 weeks ago
Benwood, West Virginia, United States
Benwood Utilities has LIFTED the boil water advisory for affected customers on S. Benwood and Browns Run areas.
The Cadiz Water Department announced Thursday morning that customers who reside on Lincoln Avenue, West Avenue, Kennedy Drive, and Short Street are no longer under the order. The order was lifted after water in the area was determined to be safe following testing.
A boil advisory for people living in the Rockway area of Springfield Twp. was lifted Thursday afternoon.
A boil advisory for parts of Danville was lifted late Thursday afternoon, according to water officials. The advisory was issued yesterday.
Type: Boil Advisory Lift
System Name - WSID#: Village Quest, LA1055070
Area Affected: All
Lift Date: 05/23/2022
Ronceverte Boil Water Advisory for Brier Hill Tank customers is LIFTED
Boiling is no longer required before consuming.
11 hours ago
A boil water advisory for the City of McFarland has been lifted. On Saturday, May 28, the Kansas Department of Health and Environment says it rescinded a boil water advisory for the City of McFarland public water supply system in Wabaunsee Co.
Columbia Water Customers located at Harrogate Rd Columbia Water laboratory staff advises the water customers of Harrogate Rd, located in Richland County, they no longer need to boil their water prior to drinking or cooking.
Recent Interesting Reports
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
Last thing eaten was a sandwich at a Law Enforcement Appreciation meeting. 5/19/2022 in Englewood Fl. Next day feeling very sick, felt cold but no fever., then vomitting, heavy trembling, somewhat incoherent. | Symptoms: Vomiting, Shaking
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
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
I purchased 2 battery powered chainsaws on June 29, 2021. (The receipt is attached) What I received 6 to 8 weeks later was not what I have ordered. Both my receipts shows item description and booths says battery powered chainsaws ×2. Wheni have contacted the store they... kept telling me it was shipped and showed to be delivered. Picture of what I received is attached. Would you kindly explain to me if what I received is a battery powered chainsaw please let me know how to use it becaus I clearly cannot see battery or chain on it. Was all the pieces sent for it. Honestly it does not look anythin like chainsaw to me. But i do wear eyeglasses and have a disability. But still I kow what chainsaw looks like. Product from China - Hahdiy.
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.
Medical marijuana products - recalled due to failed tests for mold, E. coli, yeast, and salmonella, Oklahoma, USA
3 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