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Boil Water Advisory, Glenwood, AR, USA

4 weeks ago

Glenwood, Arkansas, United States

The North Pike County Rural Water system is currently under a boil order until further notice. According to officials with the North Pike County Rural Water system, the boil order is due to a main break on the Glenwood water system.

Source: southwestarkansasradio.com
Published: 2022-09-08

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The Nelsonville Water Department has issued a boil order for the following areas in Buchtel, Marietta Avenue, Akron Avenue, North Akron Avenue, Lauderback Road, Water Street, Euclid Avenue and Franklin Avenue until 3:30PM, Friday, October 7, 2022, unless notified otherwise. This boil order is due to a... See More fire hydrant and valve repair.

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The City of White Hall water customers are on a boil order until further notice due to a water main break.

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Town in Barton County is under a boil advisory after a water main break. Officials with Mindemines said the break occurred on Main St.

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St. Martin parish Water Works District #3 has issued a subsequent boil advisory as of Thursday, October 6, 2022. Officials are informing the public of several main line water leaks in the City of Cade that are affecting Duchamp Road and all roads connected to Duchamp. The... See More boil advisory is in effect until further notice.

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A Mississippi County community is currently under a boil order advisory over issues with their water system. The Arkansas Department of Health said as of 5 p.m., Thursday, Oct. 6, the city of Dyess is under the order over “treatment interruptions” in their water system. This also... See More affects the rural water system.

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Recent Interesting Reports

I received an order I had placed and paid for the product as well as postage that had a fraudulent postage label and was I required to pay an additional $4.80 to accept the package. See Less
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East Windsor, New Jersey, Eugia US LLC (formerly AuroMedics Pharma LLC) has initiated a voluntary recall of lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial to the consumer level from the U.S. market due to... See More a product complaint for the presence of a dark red, brown and black particulate inside the vial.

Risk Statement: The administration of an intravenous product containing particulates has the potential to result in inflammation, allergic reactions, or circulatory system complications which could be life-threatening. To date, Eugia US LLC has not received reports of any adverse events or identifiable safety concerns attributed to the product consumed for this lot.

AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), contains acyclovir, a synthetic nucleoside analog, active against herpes viruses. Acyclovir Sodium Injection is indicated for the treatment of initial and recurrent mucosal and cutaneous herpes simplex (HSV- 1 and HSV-2) in immunocompromised patients and initial clinical episodes of herpes genitalis in immuno-competent patients. It is packaged in a glass vial labeled with NDC 55150-154-10. The lot being recalled is AC22006 with an expiration date of 08/2023. Eugia US LLC shipped the entire lot to wholesalers nationwide from June 8, 2022, through June 13, 2022.

The product label is as shown below: Eugia US LLC is notifying its direct consignees by recall letters and is arranging for return/ replacement of all recalled products. Wholesale customers and health professionals that have the product lot which is being recalled should immediately place the recalled lot on hold.

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 experienced 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.

Company name: Eugia US LLC
Brand name: Auromedics
Product recalled: Acyclovir Intravenous Product
Reason of the recall: Presence of a dark red, brown and black particulate inside the vial
FDA Recall date: September 27, 2022

Source: fda.gov
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The package was empty inside. It contained simply bubble wrap on bothe sides, but no contents or paper. I just came home and opened my mailbox received my electric bill a couple of standard Flyers and this manila envelope from an online seller. I was not expecting... See More any packages and I have not ordered any packages. Due to my nervous nature as it is I got outside and ripped the top of the package open and held it away from my face and pinched it open to see no contents inside just the simple bubble wrap that is on the inside of the envelope. I left it outside and I'm about to dispose of it in the trash receptacle. I'm in Crawfordville, FL, USA See Less
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GA
anonymous7079
Us too
Reply 1 week ago
L8
anonymous7082
Received one today from same.
Reply 1 week ago
Proper Trade LLC/My Stellar Lifestyle is voluntarily recalling Wonder Pill lot 20210912 and lot 31853-501, expiry 09/24, packaged in 10-count blisters co-packaged in a carton and in 60-count bottles to the consumer level. Proper Trade LLC/My Stellar Lifestyle was notified by Amazon that laboratory analysis has found... See More the product to be tainted with tadalafil, an ingredient in FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The presence of tadalafil in Wonder Pill capsules makes this product an unapproved drug for which the safety and efficacy has not been established and therefore, subject to recall.

Consumers with underlying medical issues who take the Wonder Pill with undeclared tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, Proper Trade LLC/ My Stellar Lifestyle has not received any reports of adverse events related to this recall.

The product is marketed as a dietary supplement for male sexual enhancement and is packaged in 10-count blisters co-packaged in a carton, ASIN B0B6CWC9NK, and packaged in a 60-count bottle. The affected lots include lot numbers’ 20210912 & 31853-501, Expiry 09/24. The product can be identified by the labels below. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com and Walmart at www.walmart.com, nationwide in the USA.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.

Proper Trade LLC/ My Stellar Lifestyle is notifying its customers by this press announcement and sending Amazon & Walmart messages to its customers and is arranging for return of all recalled products. Consumers that have Wonder Pill capsules which is being recalled should stop using the product.

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. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company name: Proper Trade LLC/My Stellar Lifestyle
Brand name: My Stellar Lifestyle
Product recalled: Wonder Pill Capsules
Reason of the recall: Product contains undeclared tadalafil
FDA Recall date: September 28, 2022

Source: fda.gov
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I did not order anything and yet today September 29, 2022 I received a empty package from 188 South mountain parkway Tracy, CA 95377 I'm in total shock. Why would anyone send an empty package.. See Less
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PO
p.........a
I did too
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anonymous7196
I just got one today
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This company has alot of violations they work without gloves. They also sell rotten crabs and fish to people who buy. They don’t throw anything away. The old stuff like rice with mouth poop and Rouches they mix with new ones and sell it. They leave the... See More fish out in the heat. They have a mouse and rouches problem big time. They have no Ventilations for the food or Meats. They have under age people working and Undocumented. Please send someone thats going to do the Job right in not get paid in leave.Thanks please send someone as soon as possible See Less
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I mailed a check for my deposit on a condo 9/14 and sent via certified mail. As of 9/14 the check arrived at Teterboro Distribution Center, NJ. As of 9/18, the tracking states that the letter is “in transit, arriving late, moving through network”. We are now... See More 3 business days further out with no more updates. This is a time sensitive matter and I have called USPS multiple times today. No resolution or concern on their end. They have opened a case and will “have an answer in 2-3 business days.” I have even tried calling the distribution center at 201-375-4180 - of course, no answer. I have called and left a message for consumer affairs at 732-819-3260, can’t get a live representative. No one has an answer for the delay. My fear is this is a large excuse for, we lost your letter/check. All I want is my letter delivered. If the USPS is this incompetent and can’t locate it, I want a refund for the wasted postage. I want some kind of resolution. This is absolutely horrific and holding up the purchase of my condo. See Less
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It looks they are all hitting expiry, packets i had in the house, and have seen while shopping. Not sure if it means that they will be less reliable, or not work at all. Either way, not good timing heading into fall, where covid may flare up again. See Less
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Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to a limited number of stores in AZ, CA, GA, ID, IN, MT, NM, NV, OR, TX, and UT on... See More or around May 1, 2022 through June 21, 2022 due to product being stored outside of labeled temperature requirements. To date, Family Dollar is not aware of any consumer complaints or reports of illness related to this recall.

- Products covered by this retail level recall include:

998277 COLGATE OPTIC WHITE STAIN PREVENTION TOOTHPASTE 2.1OZ
998909 COLGATE OPTIC WHITE CHARCOAL TOOTHPASTE 4.2OZ
999043 COLGATE OPTIC WHITE MOUTHWASH 16 FL OZ
999088 COLGATE OPTIC WHITE HIGH IMPACT TOOTHPASTE 3OZ
999749 COLGATE OPTIC WHITE TOOTHPASTE ICY FRESH 3.2OZ
999750 COLGATE OPTIC WHITE STAIN FIGHTER TOOTHPASTE CLEAN MNT 4.2OZ

In case you experienced harm from these 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.

Company name: Family Dollar
Brand name: Colgate
Product recalled: Toothpaste
Reason of the recall: Product was stored outside of labeled temperature requirements
FDA Recall date: September 16, 2022

Source: fda.gov
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Last 30 days