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Boil Water Advisory Lifted, Beacon Dr, Weirton, WV 26062, USA
2 weeks ago
Beacon Drive, Weirton, 26062 West Virginia, United States
Weirton Area Water Board has LIFTED the boil water advisory for Beacon Dr; East Parkway; Union Ave; Leech St; Fernwood Ave; Chrystal Ln; Patterson Dr; and Kent Way.
Beckley Water Co. has LIFTED the boil water advisory for Midway Road; Carter Avenue; Blue Room Road; Valley View Road; Ballard St; Roselawn Avenue; Brammer Avenue; Broadway Avenue; 118 1st Avenue and 246 1st Avenue.
City of Fairmont Water Dept. has LIFTED the boil water advisory for LOCUST AVENUE, RHEA TERRACE and the surrounding area.
Customers with Blue Granite Water Company were under a boil water advisory for two days, directly related to repairs made to the water distribution center. The advisory was lifted Friday for the affected neighborhoods of Bradford Estates, Keystone Commons and Planters Station Subdivision.
The Town of Coushatta Friday lifted a boil water advisory. The advisory was issued Thursday following a water main break which caused low pressure.
The Kansas Department of Health and Environment (KDHE) has rescinded a boil water advisory for the Neosho County Rural Water District 12 public water supply system located in Neosho County. The advisory was issued because of a loss of pressure in the system. Failure to maintain adequate... pressure may result in a loss of chlorine residuals and bacterial contamination.
10 hours ago
Boil-water notices have been lifted for parts of several Killeen roads. According to the city, customers affected are between 1900 and 2604 East Veterans Memorial Boulevard, 609-900 South WS Young Drive, 502 E. Veterans Memorial Blvd., 116, 204 and 207 Blake St. and 203 and 205 10th... St.
The towns of North Attleborough and Plainville said Friday their water has been “deemed safe for public use” after it was contaminated. The boil water advisory for both towns were lifted at about 4 p.m.
Recent Interesting Reports
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.
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
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!!!!
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
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.
A package delivery with "fraudulent postage applied", had to pay five dollars to get package, Amazon SJC7, 188 South Mountain House Parkway, Tracy, CA, USA
1 week ago
Ordered product awhile ago, paid overseas postage charge plus product price, should not have to pay $5.00 postage on something I already paid for.
My Yorkie is in the hospital fighting for her life after eating Dream bones. She's bleeding from the rectum severely., Huntsville, Alabama, USA
2 days 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
Lake Byllesby beach in Cannon Falls, MN closed due to E. coli, Lake Byllesby Beach, Echo Point Rd, Cannon Falls, MN 55009, USA
2 weeks ago
Lake Byllesby beach has been closed until further notice by Dakota County due to high E. coli levels. Beach water testing will resume on Tuesday, Sept. 6 when the lab reopens. Dakota County will notify the public when E.coli levels are safe for beach visitors.
Philips Respironics CPAP or Bi-Level PAP therapy masks - recalled due to potential risk of serious injury, USA
2 weeks ago
These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.
Royal Philips’ (NYSE: PHG; AEX: PHIA) subsidiary Philips Respironics is alerting... users of certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps that these devices should not be used by or near patients and their household members, caregivers and bed partners who have metallic implanted devices or metallic objects (such as metallic splinters) in the body. The magnetic headgear clips are used to attach the headgear straps to the masks, which is a method that is commonly used in the sleep therapy devices industry.
This is a voluntary notification to users of specific CPAP or Bi-Level PAP therapy masks containing such magnetic clips to inform them of the updated instructions and labeling. All users should read and follow Philips Respironics’ voluntarily updated warning and added contraindication described below. This represents a new and industry-leading practice.
Contraindication: Use of the mask is contraindicated for patients and their household members, caregivers and bed partners that may be in close vicinity to patients using the masks, that have implanted devices that may be affected by magnets, including but not limited to:
- Implantable cardioverter defibrillators (ICD)
- Magnetic metallic implants/electrodes/valves placed in upper limbs, torso, or higher (i.e., neck and head)
- Cerebral spinal fluid (CSF) shunts (e.g., ventriculo peritoneal (VP) shunt)
- Aneurysm clips
- Embolic coils
- Intracranial aneurysm intravascular flow disruption devices
- Metallic cranial plates, screws, burr hole covers, and bone substitute devices
- Metallic splinters in the eye
- Ocular implants (e.g., glaucoma implants, retinal implants)
- Certain contact lenses with metal
- Implants to restore hearing or balance that have an implanted magnet (such as cochlear implants, implanted bone conduction hearing devices, and auditory brainstem implants)
- Magnetic denture attachments
- Metallic gastrointestinal clips
- Metallic stents (e.g., aneurysm, coronary, tracheobronchial, biliary)
- Implantable ports and pumps (e.g., insulin pumps)
- Hypoglossal nerve stimulators
- Devices labeled as MR (Magnetic Resonance) unsafe
- Magnetic metallic implants not labeled for MR or not evaluated for safety in a magnetic field
Patients should stop using the affected mask if the implant/medical device is contraindicated against the mask magnets. Patients should consult their physician immediately to determine if another mask can be used for their therapy. In the interim, switch to a non-magnetic mask if available, for continued therapy.
Patients should properly dispose of the mask that has magnets after an alternative is obtained. These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.
Warning: Magnets with a magnetic field strength of 400 mT are used in the mask. With the exception of the devices identified in the contraindication, ensure that the mask is kept at least 6 inches (approx. 15 cm) away from any other medical implants or medical devices that can be impacted by the magnetic fields to avoid possible effects from localized magnetic fields. This includes household members, caregivers, and bed partners that may be in close vicinity to patients that use the masks.
Impacted masks include: More than 17 million masks containing magnetic clips have been distributed by Philips Respironics to date. As of August 30, 2022, Philips Respironics has received 14 reports of patients suggesting that the mask magnets may have impacted their medical devices including pacemaker interference, pacemaker failure leading to replacement, need of shunt adjustment, resetting of automatic implantable cardioverter defibrillator (AICD), seizures, defibrillator shutting off periodically, arrhythmia, irregular blood pressure, change in heartbeats, and cognitive issues.
Patients may contact their Durable Medical Equipment (DME) provider, which supplied the masks affected by this notice. This voluntary medical device corrective action has been reported to the regulatory agencies in the countries where these masks are available.
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: Royal Philips’ subsidiary Philips Respironics
Brand name: Philips
Product recalled: Certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps
Reason of the recall: potential risk of serious injury