IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)
Boil Water Advisory, Pine Harbor, Marion County, TX
February 1, 2021 12:00 PM
Pine Harbor, 75657 Texas, United States
The Texas Commission on Environmental Quality has required the Pine Harbor Subdivision public water system in Marion County. to notify all customers to boil their water before consumption (e.g., washing hands/face, brushing teeth, drinking, etc.). Children, seniors, and persons with weakened immune systems are particularly vulnerable to harmful bacteria, and all customers should follow these directions).
To ensure the destruction of all harmful bacteria and other microbes, water for drinking, cooking, and ice making should be boiled and cooled before drinking water or human consumption purposes. The water should be brought to a vigorous rolling boil and then boiled for two minutes.
Recent Interesting Reports
February 15, 2021 4:47 PM
“The cashier is felling sick. Every one got flu in this restaurant. This place infected with COVID 19
I got full sick. All employees are sick and needed fully attention ”
January 29, 2021 10:45 AM
“The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 43 pounds of not-ready-to-eat (NRTE), heat treated, not fully cooked chicken enchilada products due to misbranding and an undeclared allergen. FSIS is issuing this public... health alert out of the utmost of caution to ensure that consumers with allergic reactions to soy are aware that these products should not be consumed. A recall was not requested because the chicken enchilada products are no longer available in commerce.
The NRTE product labeled as “HyVee mealtime CHICKEN ENCHILADAS” was produced on Jan. 3, 2021. The following product is subject to the public health alert: [View Label (PDF only)]
62.4-oz. (3-lbs. 14.4-oz.) heat and serve container of “HyVee mealtime CHICKEN ENCHILADAS” with lot code “21003” and “Best If Use By: 01/10/2021” date on the product label. The products bear establishment number “P51558” inside the USDA mark of inspection. These items were distributed to HyVee retail locations in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.
The problem was discovered when a HyVee retail store employee identified the labeling issue and reported it to the establishment.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
For more info: fsis.usda.gov
Source: FSIS ”
February 15, 2021 1:00 AM
“I ordered 2 chainsaws from an ad on the internet which popped up while playing cards on my phone from a web company called Blackcass.com. I thought that I was ordering rechargable woodcutter/chainsaws, but received two chains instead. They would not refund my money or allow me to return and get a re... fund. They said that I had ordered the chains when I only see a big picture of a chainsaw. Their website is misleading to say the least. I would say I was scammed. They also scam people on their website with another chainsaw they are selling that has the well known brand name of Stihl on the saw. Then they send you an off brand saw made in China. Fraud indeed! ”
February 11, 2021 6:25 PM
“I did very well with my first shot of Moderna. I had no reaction except a very sore arm at the injection sight. ”
February 6, 2021 5:43 PM
“I have read the other reports and totally agree this is a scam. I thought I purchased the Stihl battery cutter shown with a hand saw in the bubble. It said $29.99 so that's what I sent. The orange handled saw arrived but not the cutter. I emailed the company and they said that was what I bought. I h... ad to click the cutter box it showed $89.99. I really liked what was advertised so I paid it. (The hand saw definitely wasn't worth $29.99 and I thought it was a gift for getting the cutter) When the cutter arrived, it was a cheap black handsaw. Came in a cardboard box not a nice carrying case. It had a small slip on guard but not the guard and shield as advertised. There was no chain saw oil. They both had charger base and battery. I emailed them back saying this was fraud. Jennifer from the company emailed back and said she was sorry about my being disappointed. I was not to send the product back. I was to send a picture of what I got, tracking number and SKU from box. I took these pictures and sent a picture of what I was promised. There was no SKU # on box. She emailed me back and said I should not return it because it could get lost going to Hong Kong and without the product there would not be a refund. She said it probably wouldn't pass customs. I should give it as a gift and person will really like it! I wrote to the Better Business Bureau and hope to find out next step. Her comments make me fearful to return. ”
I only got a chain from the Blackcass company. I ordered a little battery chainsaw , Spokane, WA, USA
February 10, 2021 6:03 PM
“On 1/20/21 I ordered the little battery chainsaw which is advertised on Facebook all the time. It cost $37.98. I only got a chainsaw blade today. ”
February 11, 2021 5:22 PM
“Got my second Moderna Covid-19 vaccine shot, no side effects this time. A little tired and thirsty but so far so good. ”
February 3, 2021 1:00 PM
“Company name: Apotex Corp
Brand name: Apotex Corp.
Product recalled: Enoxaparin Sodium Injection, USP
Reason of the recall: Packaging error resulting in incorrect dosage listed
FDA Recall date: February 03, 2021
Recall details: Apotex Corp is voluntarily recalling two (2) batches of Enoxaparin... Sodium Injection, USP to consumer level due to a packaging error resulting in some syringes barrels containing 150 mg/mL markings (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength) on the syringe barrel and vice versa. The packaging error was discovered during a customer complaint investigation. To date, Apotex has not received any reports of adverse events related to use of these two batches. The affected product is manufactured by Gland Pharma Limited, Hyderabad, India.
Health Hazard Assessment: Incorrect syringe barrel marking could lead to miscalculation and inaccurate dose administration to patients. In one recalled batch (batch CS008, strength 100 mg/mL), if a consumer used a 150 mg/mL concentration packaged in a barrel corresponding to a l00 mg/mL concentration, patients could receive 3.75 mg of Enoxaparin, instead of 3 mg of Enoxaparin. In another recalled batch (batch CT003, strength 120 mg/0.8mL), if a consumer used a 100 mg/mL concentration packaged in a barrel corresponding to a 150 mg/mL concentration, patients would receive 2 mg of Enoxaparin rather than 2.5 mg of Enoxaparin. Accidental overdosage following administration of enoxaparin sodium injection may lead to bleeding complications. Alternative, if the dose administered is less than prescribed, the patient may be subject to developing some blood clotting conditions.
Enoxaparin Sodium injection is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE), Treatment of Acute Deep Vein Thrombosis, prophylaxis of ischemic complications of unstable angina and non-Q-wave myocardial infarction, when concurrently administered with aspirin and Treatment of Acute ST-Segment Elevation Myocardial Infarction.
The affected Enoxaparin Sodium Injection, USP can be identified by NDC numbers stated on carton and label of the product.
Product: Enoxaparin Sodium Injection, USP
Batch #: CS008
Strength: 100 mg/mL
Syringe Barrel Measurement Markings: 100 mg/mL
Pack Size: 10 x 1mL Single Dose Syringes
NDC NumberOn Carton: 60505-0795-4
NDC Number On label: 60505-0795-1
UPC Code on Carton: 360505079544
UPC Code on label: (01)10360505079510
Product: Enoxaparin Sodium Injection, USP
Batch # : CT003
Strength: 120 mg/0.8mL
Syringe Barrel Measurement Markings: 150 mg/ mL
Pack Size: 10 x 0.8 mL Single Dose Syringes
NDC NumberOn Carton: 60505-0796-4
NDC Number On label: 60505-0796-0
UPC Code on Carton: 360505079643
UPC Code on label: (01)10360505079602
The two (2) affected batches of Enoxaparin Sodium Injection, USP were distributed by Apotex nationwide in the USA to Wholesalers and Warehousing Chains. Apotex Corp. is currently notifying its affected direct account Wholesalers and Warehousing Chains, via mail (FedEx Standard Overnight) by mailing a recall notification letter and is arranging for return of all recalled product.
Check the full recall details on fda.gov
Source: FDA ”
February 2, 2021 10:30 PM
“I am a female, 26 years old.An RN at Riley Children’s hospital. I received the moderne vaccine. The first dose, the physical shot was less painful than flu vaccine. Only symptom was sore arm for 2 days. Second dose, much worse. Woke up 24 hrs later feeling fatigued, nauseous, headache, and developed... large red circular rash around injection site. Lasted 24 hours. Was hot to touch and very painful. No fevers. Better the next day. ”
February 23, 2021 1:16 PM
“I ordered the Mini chain saw and the picture on the right is what i got. What the hell am i supposed to do with a chain without the saw. I am on social security and can not afford to give idiots my money. Some bastard out there is getting rich off trusting people. I want my d**n money back or i get... a lawyer. I hate a f*****g thief! ”