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Boil Water Advisory
Recent Interesting Reports
1 week ago
DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.
I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so... far today and STILL pieces of DreamBone Twist Sticks
The Procter & Gamble Company (NYSE: PG) is voluntarily recalling all lots with expiry through September 2023 of specific Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products sold in the United States, and listed in the table below, to the... consumer level due to the presence of benzene detected.
Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Based on exposure modeling and the cancer risk assessments published by the Environmental Protection Agency (EPA) (IRIS database), daily exposure to benzene in the recalled products at the levels detected in our testing would not be expected to cause adverse health consequences. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. To date, The Procter & Gamble Company has not received any reports of adverse events related to this recall and is conducting this recall out of an abundance of caution.
The affected products are used as antiperspirants and hygiene products and are packaged in aerosol cans. See the link below for Product names and UPC codes and images for further descriptions. They are recalling all lots with expiry through September 2023 of the products listed in the link below.
Company name: The Proctor & Gamble Company
Brand name: Old Spice Secret
Product recalled: Old Spice and Secret Aerosol Sprays
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 23, 2021
Check the full recall details on fda.gov
I am a 42-year-old biologist. I had very good health overall before the injection. I did suffer from seasonal allergies, but otherwise enjoyed a full and active life. I took the first Moderna injection on March 17, 2021. I took the injection because I believed it was... needed to protect myself, my family, and others in my community. I believed the FDA, CDC, and doctors that it was safe, effective, and the right thing to do. I was told that the potential side effects were possible arm pain, headache, and flu like symptoms. The CDC backed up these claims on their website by listing the side effects as minor. I took the first injection on March 17, 2021, at 9:00 a.m. at the pharmacy. A rash appeared on my arm and torso within a couple of hours. Some veins in my arms popped. There was pain on my left arm, like I had been punched. I took Allegra and slept all day from the fatigue. It only got worse from there. My doctors ignored reactions from the injection and unbelievably recommended a second shot! They said it was needed to be safe. I took the second Modern injection on June 17, 2021. After the second injection, I got dizzy right away. I stayed at the pharmacy for thirty minutes because I thought I might faint. I was fearful before the second shot. Enough that I took an EpiPen (although expired) with me as a precaution after the last reaction. Two days after the second injection, I could not even get out of bed. As the day progressed, I couldn’t perform my work on the computer. My eyesight became so blurred that I couldn’t read my email. I was dizzy when I got up. I had no choice but to stay down. That lasted at least two weeks. I still deal daily with fatigue, dizziness, memory problems, nerve pains, joint pains, burning of skin, numb ringing ears, headaches, and tingling sensations in my body. My face droops. My right hand tremors. Everyone involved in the coercion of this injection has badly harmed my daily life, my family, my work, and my health. They have taken ME away. They have taken me away from everything that made my life happy and fulfilling. Before the injection, I lived a normal, active and happy life. I worked full time, took care of my family, rescued dogs, and enjoyed a variety of physical activities. Now, I have an unnamed mysterious disorder which the doctors have told me they suspect is a variation of Guillain Bare. I suddenly have gastro issues and tachycardia. My headaches go back and forth between vestibular migraines and hemiplegic migraines. Those insane migraines take me out for hours, and sometimes days. The extreme inflammation on my brain from cytokine storm affects how I think, walk, and talk. I am unable to do the most basic tasks. Driving is completely out of the question! I cannot even drive myself anywhere, which has rendered me completely dependent on others. The effects of these shots are so extreme and never-ending. So far, no effective treatments have been found to help me. I have seen numerous specialists. I have tried special diets. I have undergone blood tests, PCP visits, neurological visits, ENT visits, cardiologist visits, immunologist visits, and many more. I have found no answers or guidance. There is no trajectory of improvement. No one knows if I will ever get better. This makes me feel really helpless and hopeless sometimes. As soon as I mention that symptoms are “vaccine” related, I feel completely ignored. No doctors want to talk about the possibility of vaccine injury. It took me six months to prove to my family doctor that I have been reacting to the “vaccine”. I spent countless hours, between the migraines and fatigue, researching desperately on my own. I even went over my medical records over the years to understand what is going on with my body. Being ignored by the medical community as well as friends and family that did not have an adverse reaction to the injection has taken a mental toll on me. At least those that live with me know the day-to-day issues and have never doubted the source. Side effects need to be acknowledged more publicly. More research needs to be done before we can push this into our kids or make mandates. Long term data is imperative and the only conscionable thing to do. | Symptoms: Other, Headache, Dizziness, Fatigue, Gas, Joint Pain
2 weeks ago
I have been applying since the beginning of the month I went to two different appointments and every three hours the system messes up and thinks that I haven’t done my steps
MaryRuth’s, a leading omni-channel health and wellness brand that offers vitamins, minerals, and supplements for the entire family, today announced that, out of an abundance of caution, it is voluntarily recalling two lots of its liquid probiotic for infants (1oz) due to the possibility of contamination by... Pseudomonas aeruginosa.
Pseudomonas aeruginosa is a microorganism found in the environment that, if ingested, can cause infection in immunocompromised individuals or, rarely, in very young infants. P. aeruginosa infections in immunocompromised infants are generally limited to hospital settings. In such settings, there is the chance that the infant’s immature gut will not be able to prevent P. aeruginosa from gaining access to the blood, and from there it can disseminate elsewhere in the body, resulting in the possibility of serious adverse health consequences.
This recall only affects two lots of the product, Lot #100420218 and Lot #100520218, UPC barcode number 856645008587. Lot numbers are located on the side of the bottle and on the bottom of the outer container in which the product is sold. No other lots or any other MaryRuth’s products are affected by this recall. This product is distributed nationwide through Target, Amazon, and direct sales from the company’s website.
The company is asking consumers to throw away product from both affected lot numbers. The company discovered the potential issue with one of its manufacturing partners during routine laboratory testing.
The only product complaint the company has received with respect to the affected product lots was one report of temporary diarrhea in an older infant after consuming the product, which the company does not believe was related to the presence of the microorganism.
Company name: MaryRuth’s
Brand name: MaryRuth’s
Product recalled: liquid probiotic for infants
Reason of the recall: Potential contamination with Pseudomonas aeruginosa
FDA Recall date: October 29, 2021
Check the full recall details on fda.gov
Nag Champa Incense Caused Abnormal Allergic Reaction In Dog With This Particular Package of It, Archimage, Monroe Avenue, Rochester, NY, USA
2 weeks ago
Usually is fine. Not this time. I decided to burn Nag Champa incense to meditate. As I was meditating, our dog started sniffling and then began throwing up large amounts of mucous. Her lips were swollen and pulled back slightly. She is ok now, but I've never... experienced anything like this using incense before this happened. I often use it for meditation. I called the vet who confirmed this is an allergic reaction and they informed me to monitor her and ensure she is safeand healthy, not vomiting anymore. They instructed me to open all the windows and doors, turn on ceiling fans,and run the furnace heat to pull remaining particulate into the HEPA filter on the furnace and then to replace the filter tomorrow to ensure it doesn't just recirculate the particulate if any happens to get through. Also said to wash hard surfaces in the room it was burned on and vacuum up any furniture,carpet, or rugs there to remove any settled particulate. I'm not sure what went wrong here. I've never had this happen with her or any other dog when burning this.
But even I am sniffling and nauseous after having burned it and my throat is sore. I took benedryl to
prevent an attack in me personally.
Nag Champa incense sticks.
Label information: Nag Champa Agarbatti Satya Sai Baba. Mfrs. Shrinivas
Sugandhalaya(BNG)LLP.1/9,8th Cross, Magadi Road, Bengaluru-560023, India. Certified green
product. Export Quality.2021 Series. Hand Rolled in India. UPC 8904245400491.Warning: insist for this label to avoid imitation buy from reputed dealers only. Earth. Contains seals with hologram over each side of the box with official logo. NetWt.40g. Quality assurance labels are not actual stickers demonstrating actual checks, but are instead printed onto the package to appear as if they were actual quality assurance stickers and are offset with a white background to trick a consumer. There are three which areas follows. Fake QA sticker1: Quality Assurance Management ISO 9001(check mark symbol)
Fake QA sticker2: Environmental Management ISO 14001(check mark symbol) Fake QA sticker 3: Occupational Health &
Safety OHSAS 45001 (check mark symbol).
Customer care number+917022000111
Item purchased at Archimage. Not their fault. They only buy reputable authentic items and this has to be a bad or contaminated batch here. | Symptoms: Nausea, Other
FOR IMMEDIATE RELEASE – November 19, 2021 – American Screening LLC of Shreveport, Louisiana is voluntarily recalling 153,336 units of Hand Sanitizer, containing 70% ethyl alcohol gel to the consumer level. The hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk... of consumption.
Risk Statement: Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute. To date, American Screening LLC has not received any reports of adverse events related to this recall.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in an eight ounce bottle. The affected hand sanitizer lots include the following expiration dates of 5/21/2022 and 05/24/2022 for black capped bottles and no lot numbers or expiration dates for clear capped bottles. The product can be identified by its shape (small water bottle), with a black flip top cap or clear cap with blue pouring spout with the weight of measure of eight (8) ounces/237mL, UPC 8 4005051579 2.
The Hand Sanitizer was sold to customers & distributors Nationwide via the internet at americanscreeningcorp.com and/or in-house sales.
Consumers & distributors that have this hand sanitizer which is being recalled should stop distribution/use and return to place of purchase or discard. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to ingesting the hand sanitizer packaged in the 8 oz. water bottle style.
Company name: American Screening LLC
Brand name: American Screening
Product recalled: Hand Sanitizer
Reason of the recall: Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption
FDA Recall date: November 19, 2021
Check the full recall details on fda.gov
Arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm., USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
1 week ago
I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT
1 week ago
Package was supposed to be delivered November 6, 2021.
After days of endless calls finally told it left teterboro post office November 5 but was never delivered or tracked since.
CHICAGO, IL – November 19, 2021 - Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of four lots of Levetiracetam Injection, USP, to the user level. The lack of container closure integrity, found in reserve sample vials may result in a non-sterile product.
Risk Statement: Intravenous... administration of a product intended to be sterile that is not sterile could result in serious systemic infections which may be life threatening.
To date, Sagent has not received reports of any product complaints or adverse events associated with this issue. Levetiracetam Injection, USP 500 mg per 5 mL, is used in the treatment of certain types of seizures and is packaged in a 5mL single-does vial. The Levetiracetam Injection, USP, label and affected lot numbers with Expiration Dates and NDC number can be found in the table below.
Product: Levetiracetam Injection, USP / Lot Number: B0G85VB /Expiration Date: Jun-2022 / NDC Number: 25021-780-05 / Distribution Dates: May 2021 - August 2021.
Product: Levetiracetam Injection, USP / Lot Number: B0K88VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: March 2021 - November 2021.
Product: Levetiracetam Injection, USP / Lot Number: B0K89VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: August 2021 - November 2021.
Product: Levetiracetam Injection, USP / Lot Number: B1G194A /Expiration Date: Jun-2023 / NDC Number: 25021-780-05 / Distribution Dates: October 2021.
Product was distributed Nationwide from March to November 2021.
Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Levetiracetam Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: November 22, 2021
Check the full recall details on fda.gov