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Boil Water Advisory fully lifted in Baltimore, officials say no further contamination detected
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The Kansas Department of Health and Environment (KDHE) has rescinded a boil water advisory for the Neosho County Rural Water District 12 public water supply system located in Neosho County.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.
2 days 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.
The boil advisory for the City of Marksville customers has been lifted. The advisory still remains in place for Spring Bayou customers. If you have any questions, please contact Spring Bayou Water System.
Wheeling Water Dept. has LIFTED a boil water advisory for Mt. St. Joseph's; Oglebay Speidel Golf Course; Oglebay Central Receiving; and 3 Beever Lane.
Recent Interesting Reports
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.
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.
My Yorkie is in the hospital fighting for her life after eating Dream bones. She's bleeding from the rectum severely., Huntsville, Alabama, USA
4 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
3 weeks ago
DeWitt Park beach is closed to swimming by Kenosha County Public Health, testings showed elevated E.coli levels.
The result at DeWitt that triggered the closure was >2,419 E.coli/100 mL. That location was scheduled to be resampled Tuesday. More results are expected to be available Wednesday.
One of You’re big rig 3 axle trucks is driving down this road Country Club drive Roseville CA, 8:15 am. 09/09/2022 (he was also speeding). this is not a truck route! Amazon is in violation of the FMCSA rules.
2 weeks ago
5 days ago, I began usage of CVS Salicylic Acid Wart Removal Strips that contain 40%
salicylic acid. I have used them for about 5 days. Over the last five days around day two
I began having bouts of nausea but never attributed it to this. The... following day began
stomach cramps and pain. Today my left side of my back is burning deep inside
around the kidney area. I have excessive thirst not being fixed by drinking water. My
vision is blurry and I also have an awful taste in my mouth. The taste in my mouth is
exactly what the scent of these strips is. I looked up and then contacted a poison
control center and it is suggested this may be a case of Salicylic Acid poisoning from
this product. The occurrences over this short span ae far too coincidental for this to not
be the case. Upon further research it is nearly identical to a case in 2008 in which a
pediatric patient exposed to a similar product experienced similar symptomatology that
was determined to be a poisoning by this type of product. These products are not safe.
The product has been used on the left pointer finger below the middle knuckle. There is
some area of skin that has sloughed off and was bright pink earlier and is now white.
The finger itself feels off like neurologically off and partially numb currently. It has now
been 24 hours since I began this report and the symptoms are beginning to subside
slightly. It is a slow subside though. The only thing different today is my kidney does
not hurt constantly now it is off and on but much less intense and easing as time goes
on more so. The nausea has subsided. The taste however still remains in my mouth but
is slightly less than before but not enough yet. The other remaining symptoms include
stomach cramping, some nausea off and on but no longer constant, bloating, I
experienced measured tachycardia as well as a burning sensation along the left hand
side of the mid back right below the rib cage ending. This pain has subsided but is still
occasionally present for a split second then gone. | Symptoms: Cramps, Blurry vision
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.
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