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Boil Water Advisory, Crescent Drive, Killeen, TX, USA
1 month ago
Crescent Drive, Killeen, 76543 Texas, United States
Killeen city officials issued a boil-water notice for a large neighborhood in north Killeen, the city announced Monday afternoo. The affected addresses are:
3200 - 3613 Crescent Drive
2601 - 2813 Boswell Drive
2901 - 3108 Blue Ridge Drive
3400 - 3611 Northcrest Drive
2801 - 2804 Northcrest Circle
3400 - 3611 Westview Drive
3400 - 3613 Warfield Drive
3402 - 3407 Boswell Circle
15 hours ago
There is a precautionary Boil Water Advisory in effect within the potable water system in Cypress Lakes. The precautionary boil water notice will remain in effect until a satisfactory bacteriological survey is received. Customers will be notified once the boil advisory has been rescinded.
15 hours ago
Charlotte County Utilities has declared a precautionary boil water notice for all customers. The boil water notice will remain in effect until further notice.
The Turkey Creek Water System has issued a boil advisory for the area between JNOG Lewis Jr. Dr. and I-49 due to routine line maintenance.
11 hours ago
A Precautionary Boil Water Noitce Advisory has been issued to all 314 FGUA Tangerine System customers in Mount Dora, following a loss of power to the treatment plant, and a generator malfunction. The loss of pwer and generator failure caused a system-wide loss of pressure currently being... experienced in the system.
11 hours ago
The Florida Governmental Utility Authority (FGUA) has experienced a loss of water service to all Rosalie Oaks System customers due to a loss of electrical service at the Rosalie Oaks Water Treatment Plant due to Hurricane Ian. The service was first reported as interrupted at approximately noon... today. Following restoration of service, a Precautionary Boil Water Notice Advisory will be in effect, and will be rescinded once water samples taken to a Florida Department of Health-certified laboratory indicate that the water is safe to drink, typically 48 hours after restoration of water service.
11 hours ago
The Chuluota water system has experienced a loss of power due to Hurricane Ian. Power was restored, however, the current pressure dropped below 20 PSI and requires a boil water notification and clearance. A Precautionary Boil Water Notice Advisory will be in effect.
11 hours ago
City of Winter Springs water customers are under a Boil Water Advisory. As a precaution, it is advised that all water used for drinking, brushing teeth, or food prep/cleanup be boiled.
11 hours ago
Ringling Bridge is open to all now. Water & sewer services have been restored. A boil water notice is in effect for the barrier islands until at least 1 pm Saturday.
Recent Interesting Reports
bought product from Stuncloth, freshlook colorblend Gray contacts. Instead sending me what I ordered and PAID for I received MAXIY BROWN CONTACTS. This what I ordered AND IT WAS ALSO CONFIRMED IN THE EMAIL I RECEIVED BELOW. Items in this shipment Freshlook Colorblends Colored Contacts Lenses Non... Prescription (Buy 3 get 1 Free) × 2 Gray. I WANT MY MONEY BACK, OR THE PRODUCT THAT ORDERED AND PAID FOR!!!!
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... 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
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... 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.
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.
1 week ago
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 inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being stored outside... of labeled temperature requirements. This notice covers the recall of Over-the-Counter Medical Devices. An earlier notice issued July 21, 2022 covered a related recall of Over-the-Counter Pharmaceutical Products. To date, Family Dollar has not received any consumer complaints or reports of illness related to this recall. This recall is being conducted out of an abundance of caution.
- Recalled products:
900260 900260 CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT
900794 900794 LS SKYN NON LATEX LUBRICATED CONDOM 3CT
901260 901260 VERIQUICK PREGNANCY TEST 1CT
902343 902343 FIRST RESPONSE 2 CT
903409 903409 SKYN ORIGINAL NON LATEX CONDOM 12CT
903415 903415 SKYN ELITE NON LATEX CONDOM 12CT
939504 939504 VERIQUICK PREGNANCY TEST 1 CT
900752 900752 AT HOME MARIJUANA TEST STRIP
902816 902816 TROJAN ULTRA RIBBED LUBED 3CT
903756 903756 VERIQUICK PREGNANCY TEST 2 CT
999763 999763 TROJAN ULTRA THIN CONDOM LATEX 3CT
998221 998221 SKYN ELITE LARGE NON LATEX CONDOM 12CT
998869 998869 PREFERRED UTI TEST 1 CT
900265 900265 LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT
900531 900531 CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO
999009 999009 B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ
902274 902274 GS SALINE SOLUTION 12FL OZ
901443 901443 KY JELLY LUBRICANT 2 FL OZ
901960 901960 OPTI FREE REPLENISH MULTI PURPOSE 2 OZ
999801 999801 SIMPLY SALINE NASAL MIST 3.1 OZ
900457 OPTI FREE PURE MST DSINFCTNG SLTN 4FL OZ
902139 902139 DENTEMP ONE STEP .077OZ
906018 906018 FIXODENT ORG CREAM 2.4OZ
998762 998762 DRTALBOT TDDLR TTHPSTE BRSH TUTTI FRUTTI
905076 905076 CURAD STRNG WATRPRF STRIP 1IN 20CT
906312 906312 GS DENTURE CLEANSER GRN TAB 40CT
999619 999619 FIXODENT ADH CREAM ULTRA MAX HOLD 2.2OZ
999037 999037 CURAD FIRST AID KIT
903377 903377 POLIGRIP POWER MAX HOLD 2.2OZ
999417 999417 NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ
900737 900737 TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT
901239 901239 FIXODENT ORG CREAM TRAVEL .75OZ
906131 906131 POLIDENT DENTURE CLNS TAB 28CT
900334 900334 POLIGRIP ADH CREAM FREE 2.4OZ
906023 906023 GS DENTURE CLEAN OVRNT TAB 40CT
901634 901634 POLIDENT DENTURE CLEANSERS 84 CT
901777 901777 POLIDENT OVERNIGHT WHITENING TAB 28CT
906402 906402 FIXODENT ADH CREAM WITH SCOPE 2OZ
999632 999632 POLIGRIP EXTRACARE ADHESIVE CREAM 2.2OZ
900085 900085 SUPER POLIGRIP ADH CREAM .75OZ
900723 900723 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ
This recall goes to the retail store level. Not all of the products listed were sent to all stores. Family Dollar has notified its affected stores asking them to check their stock immediately and to quarantine and discontinue the sale of any affected product. Customers that may have bought affected product may return such product to the Family Dollar store where they were purchased without receipt.
This recall does not apply to Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont, Washington, Alaska, or Hawaii as Family Dollar does not have any stores in Alaska or Hawaii and no Family Dollar stores in any of the other states received any products subject to this recall. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products.
Company name: Family Dollar
Brand name: Multiple brand names
Product recalled: Various OTC medical products
Reason of the recall: Product was stored outside of labeled temperature requirements.
FDA Recall date: September 16, 2022
13 hours ago
I received this package and nothing is in it the tracking number is 9400136206335672417717 I paid for this item I want what I paid for
Received an empty package - from 188 South Mountain house Parkway Tracy CA 95377, 188 South Mountain House Parkway, Tracy, CA, USA
9 hours ago
Although I received an empty package from 188 South Mountain house Parkway Tracy CA 95377 the 1st class postage says mailed from zip 90021 on September 24, 2022.
I got this covid booster, and flu shot at the same time. Zero side effects so far, and I am on day 3 now. I assume by now I am in the clear. The picture says moderna, but he assured me it was the pfizer.
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... 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
My Yorkie is in the hospital fighting for her life after eating Dream bones. She's bleeding from the rectum severely., Huntsville, Alabama, USA
1 week ago
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