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Boil Water Advisory, Bunnell, Fla, USA
2 weeks ago
Bunnell, Florida, United States
A boil water order has been issued for customers in Bunnell in Flagler County. According to City officials, there was a power outage that temporarily shut down the water treatment plant and interrupted service to the entire city on Monday night.
Source: wftv.com
Published: 2023-11-14
12
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Boil Water Advisory, Bunnell, FL, USA
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A power surge this morning briefly knocked the Bunnell water plant off line, interrupting water service city-wide, Bunnell City Manager Alvin Jackson said. The interruption resulted in a cautionary boil-water advisory for residents and businesses across the city. Water service was restored, but since the water pressure... See More fell during the interruption, a precautionary boil water notice was issued, and will be in effect for up to three days, depending on testing.
Source: flaglerlive.com
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Boil Water Advisory, Bunnell, FL, USA
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Boil water notice issued in Bunnell after storms
Source: spotonflorida.com
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Power Outage, Bunnell, FL, USA
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Severe storms on Saturday caused a power outage
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Source: clickorlando.com
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Employee test positive for Covid-19, Bunnell Elementary School, 305 N Palmetto St, Bunnell, FL 32110, USA
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I fed my puppy a dream bone twist and now she's throwing up and very weak, Illinois, USA
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Noah’s Wholesale, LLC is voluntarily recalling one lot of rock# 03032021, exp:12/2027, 1200 mg/capsule, to the consumer level. FDA analysis has found the product to be tainted with Sildenafil. The product was distributed locally through convenience stores and some island jobbers (small wholesale distributors to retail). Noah’s... See More Wholesale has not received any reports of adverse events related to this recall to date.
Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) found in FDA-approved products for the treatment of male erectile dysfunction. The presence of sildenafil in this product renders the rock an unapproved drug for which the safety and efficacy have not been established and, therefore, subject to recall.
Risk Statement: Consumption of products with undeclared sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life-threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.
The Rock is marketed as a dietary supplement for male sexual enhancement and is packaged as a single pill in a blister pack. It is labeled as ORIGINAL THE ROCK, Male sexual performance, with the following UPC 6 61799 95052 7. Distributed by: Steele Products, Hallandale, FL. The Rock affected lot is lot#03032021, Exp:12/2027. The product can be identified by the red and black lettering on a white-flat small cardboard package with one red capsule seen through a clear blister window.
Noah’s Wholesale is notifying its distributors and customers by phone, emails, and through their sales representative and is arranging for a full refund/credit of all recalled products. Consumers who have the recalled product should stop using the product and return it to the place of purchase or discard the product immediately. Distributors and retailers should stop selling the product and contact Noah’s Wholesale LLC for a refund process.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
In case you experience harm from this product, 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.
Company name: Noah’s Wholesale, LLC
Brand name: Noah’s Wholesale, LLC
Product recalled: Dietary Supplement with undeclared Sildenafil
Reason of the recall: Undeclared drug, Sildenafil
FDA Recall date: November 21, 2023
Source: fda.gov See Less
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Hi,I did received a package from this company a drone that I didn't order..Iam a62 year old senior don't know how to even operate my E- mails... Please help I just want to return it...but no address provited..Just credit my account, accorndently...
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SugarMDs, LLC is voluntarily recalling Lot: 22165-003 Advance Glucose Support Supplement in 60, 120 and 180 count bottles to the consumer level. FDA analysis has found the product to be tainted with glyburide and metformin. The product was distributed Nationwide in the US -through internet sales via... See More amazon and their website. To date, SugarMDs LLC has not received any reports of adverse events related to this recall.
Glyburide and Metformin are active ingredients found in several FDA-approved prescription drugs used to treat type 2 diabetes. Products containing glyburide and metformin cannot be marketed as dietary supplements. Advanced Glucose Support Supplement is an unapproved new drug for which safety and efficacy have not been established and, therefore, subject to recall.
Risk Statement: Glyburide may pose serious and potentially life-threatening risks to consumers because this ingredient may result in unsafe drops in blood sugar levels (hypoglycemia). Common symptoms of hypoglycemia include fast heartbeat, shaking, sweating, nervousness or anxiety, irritability or confusion, dizziness, drowsiness, headache and hunger. Hypoglycemia may quickly become severe, resulting in seizures, coma or death. Metformin may pose a serious risk to consumers because this ingredient can cause a rare but serious side effect called lactic acidosis (a build-up of lactic acid in the blood) that can cause death if untreated. Symptoms of lactic acidosis include nausea, vomiting, fatigue, body aches, respiratory distress, abdominal pain and fast, deep breathing. Metformin may also cause hypoglycemia when taken together with other medications to lower blood sugar.
This tainted Advanced Glucose Support is marketed as a dietary supplement and is packaged in:
- 60 count bottle : UPC code 00195893927678 (UPC code located below the "Supplement Facts" panel)
- 120 count bottle: UPC code 00195893546978
- 180 count bottle: UPC code 00195893999576
An example product label can be found in the picture attached. The affected Advanced Glucose Support lots include the following: Lot# 22165-003 EXP: 09/2024
SugarMDs LLC is notifying its distributors and customers by email and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using and return to place of purchase for a full refund. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experience harm from this product, 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.
Company name: SugarMDs, LLC
Brand name: Dr. Ergin’s
Product recalled: SugarMD Advanced Glucose Support, Dietary Supplement
Reason of the recall: Undeclared Glyburide and Metformin
FDA Recall date: November 15, 2023
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