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Boil Water Advisory, Olive St, Shadyside, OH 43947, USA

1 month ago

Olive Street, Shadyside, 43947 Ohio, United States

Water will be turned off around 2:30 p.m. Tuesday from West 38th to West 40th streets and from Central Avenue to Daisyview in Shadyside. This is for a valve replacement. The water will be off until the work is done. There will be a 48-hour boil order in place.

Source: twitter.com
Published: 2022-09-06

100


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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.

Source: twitter.com
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WV American Water has expanded the boil water advisory in the Lake Drive area of Glade Springs to include Lake Dr between Long Dr and Teaberry Ct; Resort Dr; Chestnut Hill Lodge; and the Manor Houses.

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A boil order has been issued until further notice for buildings on Illinois College campus along Mound Road from Lincoln Ave. to Park Street. This is due to a water main break at Lincoln and Mound Ave.

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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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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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Electric power was knocked out to parts of Logan early this morning (Friday, Oct. 7) when a large dump truck whose driver had neglected to lower the vehicle’s dump bed tore down traffic lights and utility lines above state Route 93/Mulberry Street at the intersection with Front... See More Street. Power was out to many nearby businesses as of around 9:30 a.m. Friday.

Outage link: outagemap.aepohio.com.s3.amazonaws.com
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Recent Interesting Reports

Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This voluntary... See More recall only affects products with lot# GS046745. No other Clopidogrel or Atenolol products marketed by GSMS, Inc. are impacted. Both products are being recalled out of abundance of caution.

-Recalled products:
Product Description: Clopidogrel 75mg Tablets, 1,000 Count Bottle, GSMS NDC: 51407-032-10, Lot #: GS046745, Expiration Date: 12/2023
Product Description: Atenolol 25mg Tablets, 1,000 Count Bottle, GSMS NDC: 60429-027-10, Lot #: GS046745, Expiration Date: 12/2023

Atenolol tablets are indicated for the treatment of hypertension, to lower blood pressure. Clopidogrel is prescribed to lower the risk of having a stroke, blood clot, or serious heart problem for patients who have had heart attack, severe chest pain, or circulation problems as indicated in the product labeling. For more drug label information about clopidogrel bisulfate visit: DailyMed - CLOPIDOGREL- clopidogrel bisulfate tablet, film coated (nih.gov). For more drug label information about atenolol visit: DailyMed - ATENOLOL tablet (nih.gov)

Patients who suddenly stop taking atenolol, as would happen if clopidogrel were misplaced in the atenolol-labeled bottle, are at increased risk for ischemic (angina, myocardial infarction), hypertensive and arrhythmic adverse events relating to rapid withdrawal of beta antagonism. Further, patients who are on atenolol are frequently on concomitant anticoagulant and antiplatelet medications and would be at increased risk for bleeding if clopidogrel were added to the regimen. To date, GSMS, Inc. has not received any reports of adverse events related to the use of the products as part of this recall.

The lot under GSMS, Inc.’s voluntary recall has been primarily sold to AmerisourceBergen, and McKesson. AmerisourceBergen and McKesson are instructed to immediately stop distribution, quarantine all remaining products in their control, and return the recalled product to GSMS, Inc. They are also instructed to provide their customers, i.e., pharmacies and consumers, a copy of GSMS, Inc.’s recall notification, recall response form, and letter to consumers, patients, and caregivers.

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

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: Golden State Medical Supply, Incorporated
Brand name: Golden State Medical Supply, Incorporated
Product recalled: Clopidogrel 75mg Tablets, Atenolol 25mg Tablets
Reason of the recall: Due to Label Mix-up
FDA Recall date: September 29, 2022

fda.gov
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466


This package was delivered addresses to me, I didn’t order it but it came from an online seller at 1555 N. Chrisman Riad in Tracy, CA 95304 See Less
819


She began to have diarrhea 3 days ago after eating the first Dream bone. We didn't relate the problem. She got a second one the next day and the diarrhea continued for 3 days. Last night blood began to pour from her. Today they are trying to see where the bleeding is coming from to save her. | Symptoms: Diarrhea, Bloody Stool See Less
301


I received an empty bubble mailer approximately 4 x 6 from an online seller at 188 South Mountain House Parkway, Tracy, CA 95377. Said it was mailed from zip code 90021. Received on 9/28/2022. See Less
3.1K


GL
G...........l
I received the same package today. My package was empty as well.
Reply 1 week ago
YX
anonymous7118
I did too.
Reply 1 week ago
X6
anonymous7123
Mee too!!
1 Reply 1 week ago
DE
d.................w
Mine had a very low quality large caffeine and gasoline shirt
Reply 1 week ago
WF
w.....9
I did too on 9/29
Reply 1 week ago
H9
anonymous7127
Mine came today as well
Reply 1 week ago
LI
l.............e
I did to today.
Reply 1 week ago
KR
k..............3
I just got the same thing
Reply 1 week ago
I3
anonymous7132
Same
Reply 1 week ago
AN
a..........d
I did also
Reply 1 week ago
DA
d.........a
I received an empty package with nothing in
Reply 6 days ago
WN
anonymous7149
Same here. Empty envelope
Reply 6 days ago
UF
anonymous7156
same what is up with this? i wonder if it is a scam of some kind.
Reply 6 days ago
IA
anonymous7161
Empty envelope
Reply 6 days ago
CM
c....6
I did also today, same story, did you by any chance order anything from on facebook? I did thats why I'm asking so I'm wondering if its connected to that
Reply 5 days 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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466


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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Last 30 days