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The Kansas Department of Health and Environment (KDHE) has rescinded a boil water advisory for the City of Olsburg public water supply system located in Pottawatomie County. The advisory was issued because of a loss of pressure in the system.
(SEND ON 09/24)A water system shutdown next week is prompting a boil water advisory for the Town of New Windsor Water System. A water leak repair and valve replacement project will begin at about 9 a.m. Monday, Sept. 26. Due to the possibility for untreated water and... bacteria to enter the system, affected residents are being advised to boil their water for 2-3 days after water is restored. Affected communities include Vails Gate Heights Drive, Mountain View Village, Old Forge Hill Road, Vails Gate School, and Big V Plaza Businesses.
A boil water notice is in effect for parts of Marion County. The notice is in effect for residents east of Big Oaks Subdivision on FM 729 to the Alley Creek Park area, all county roads off of FM 729 within this service area, Deer Cove, Woodland... Shores and Alley Creek Park. A line break on FM 729 has caused a drop in water pressure meaning that residents should boil their water, according to Mims Water Supply Corp.
A boil water advisory is in place for multiple Pittsburgh neighborhoods after a water main break. The Pittsburgh Water and Sewage Authority said an 8-inch water main broke on Steuben Street at around 8:15 p.m. Thursday. The advisory is in effect to protect approximately 600 homes from... contaminants that may have entered the water when pressure was low.
WATER MAIN BREAK. If pressure has been restored & you are experiencing cloudiness, run faucet to flush lines until water clears. Anyone with boil water advisory will be notified door to door: Affected 1294-1726 Hartford Ave, Horseshoe Ave, Manning Dr, Sherman Rd, Hollow Dr.
City of Fairmont Water Dept. has issued a boil water advisory for Firehouse Rd. Deerhaven Dr., Ross St., East Ln., Sabina St., Trey Ln., and the surrounding area.
Residents living near Acacia Road and State Road A1A were placed under a 72-hour boil water notice after a water main break Thursday.
A boil water notice has been issued for N.E.W. Water Supply due to electrical issues at a plant on Friday. The customers affected are on FM 711, CR 203, CR 205, CR 223, Harmony, Fountain Town, and Woodland Acres Communities.
A scheduled potable water main shutdown on Everest Parkway has been rescheduled for Monday, Oct. 3 at 9 a.m. in an abundance of caution due to a tropical storm possibly affecting the city of Cape Coral next week. The work was originally scheduled for Monday, Sept. 26.... Residents who will be affected will be notified via phone, email, text message, and door tags. Following the restoration of access to drinking water, we advise users to boil water for one minute or use bottled water as a precaution until the advisory has been lifted.
Recent Interesting Reports
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.
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.
Veterans Park Bathing Beach closed due to high levels of E. coli, Veterans Waterfront Park, 98-158 W Spring St, Port Austin, MI 48467, United States
3 weeks ago
Veterans Park Bathing Beach in Port Austin is closed until further notice due to high levels of E. coli.
The Huron County Health Department collected the latest bathing beach sample results on Aug. 29. According to Health Department, the samples collected can not exceed 300 E. coli... colonies per 100 ml of water.
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
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
Spot and Tango announced the recall of 4 batches of their Chicken and Brown Rice UnKibble Dog Food because samples tested positive for Salmonella bacteria.
The recalled product is Chicken and Brown Rice UnKibble Dog Food, with the codes:
-Lot Code T-22220 and SKU Number U-C-004
-... Lot Code T-22223 and SKU Number U-C-005
- Lot Code T-22220 and SKU Number U-C-006
- Lot Code T-22228 and SKU Number U-C-003
No other Spot & Tango products are affected by this recall.
Salmonella can affect animals eating the product and there is risk to humans from handling contaminated products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.
Dogs with Salmonella infections will most likely not exhibit any symptoms, though in rare cases they may be lethargic and have diarrhea (which may be bloody), fever, and vomiting. Some dogs may have only decreased appetite, fever, and abdominal pain. Infected but otherwise healthy dogs can be carriers and infect other animals or humans through the fecal-oral route.
If you have the recalled product in your home, please stop feeding it to your dogs and dispose of it immediately.
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.
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!!!!
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