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Boil Water Advisory in place, Sophia, WV, USA
January 27, 2021 12:00 PM
Sophia, West Virginia, United States
Boil water advisory for Raleigh County PSD for Arnett customers, Garnet Lane to and including Pine Branch, due to a water main line break.
Customers are advised to bring all water to a full rolling boil, let it boil for one minute and let cool before using, or use bottled water.
Boiled or bottled water should be used for drinking, making ice, brushing teeth, washing dishes, bathing, and food preparation until further notice. Boiling kills bacteria and other organisms in the water.
Source: register-herald.com
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Recent Interesting Reports
Public Health Alert for HyVee mealtime CHICKEN ENCHILADAS Due to Undeclared Allergen, Georgia, USA
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... See Morehealth 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 See Less”
Covid 19 vaccine symptoms, Indianapolis, IN, USA
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... See Morelarge red circular rash around injection site. Lasted 24 hours. Was hot to touch and very painful. No fevers. Better the next day. See Less”
Blackcass.com or funny456, scam, Houston, TX, USA
February 11, 2021 11:05 AM
“Dont order any thing from black cass or funny 456 both r scams i order two saws and got two chains thats it i order a fold up scooter from funny456 and got a charger to what i do not know both arw full of crap and iam out money See Less”

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... See MoreSodium 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 See Less”
Black Cass chain saw scam., Glencoe, Arkansas, USA
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... See Morea lawyer. I hate a f*****g thief! See Less”
blackcass atg-26 battery chainsaw, Indianapolis, IN, USA
February 12, 2021 3:09 PM
“Blackcass, 2020 Hot Selling-GTA 26 Battery-Powerd Wood Cutter is what I ordered- said it was a stihl model- including case- did not recieve that- have an off brand no case :(not stihl gta-26 model See Less”
February 10, 2021 10:00 PM
“Company name: NDAL MFG INC
Brand name: ManukaGuard
Product recalled: Allercleanse Nasal Spray
Reason of the recall: Due to Yeast Contamination
FDA Recall date: February 10, 2021
Recall details: NDAL MFG INC is voluntarily recalling one lot of Manukaguard Allercleanse, nasal spray to the consume... See Morer level. The Allercleanse nasal sprays have been found to be contaminated with yeast.
Risk Statement: The use of Allercleanse (manuka honey) nasal spray contaminated with yeasts, in the population most likely to use it (children, adults, and elderly), may result in adverse events that necessitate medical or surgical intervention. However, use of this contaminated product in immunosuppressed individuals may result in life threatening invasive fungal infections.
NDAL MFG INC has not received any reports of adverse events related to this recall. The product is used as a NASAL SPRAY to clean nasal passages and sinuses of irritants and other environmental contaminants and is packaged in cardboard box with one nasal spray per box UPC 858631002128. The affected Allercleanse lot is lot # 2010045 and BB 10/2023 expiration date.
Product was distributed Nationwide in the USA to 1 e-commerce website amazon.com, distributors and retail stores. NDAL MFG INC has notified its distributors and customers by e-mail followed by telephone and further email and has arranged for return/replacement etc. of all recalled products.
Consumers/distributors/retailers that have product which is being recalled should stop using/return to place of purchase/discard/contact their doctor, etc., if they have not already done so. Consumers with questions regarding this recall can contact NDAL MFG INC by phone 1-800-916-1220 or e-mail address SUPPORT@MANUKAGUARD.COM, M-F 7:30 am to 4 pm PST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Check the full recall details on fda.gov
Source: FDA See Less”
Alternative Foods London recalls OGGS Zesty Lemon Cake because of undeclared soya, UK
January 29, 2021 10:47 AM
“Alternative Foods London Ltd is recalling OGGS Zesty Lemon Cake because it contains soya that is not declared on the label. This means the product is a possible health risk for anyone with an allergy to soya.
Product details
OGGS Zesty Lemon Cake
Pack size 386g
Best before 26 January 2021; 02... See MoreFebruary 2021; 09 February 2021 and 16 February 2021
Allergens Soya
Risk statement
Allergen(s): Soya
This product contains soya making the product a possible health risk for anyone with an allergy to soya.
Alternative Foods London Ltd is recalling the above product from customers and has contacted the relevant allergy support organisations, which will tell their members about the recall. The company has also issued a point-of-sale notice to its customers. These notices explain to customers why the product is being recalled and tell them what to do if they have bought the product. Please see the attached notice.
If you have bought the above product and have an allergy to soya, do not eat it. Instead return it to the store which you purchased it for a refund.
Check the full recall details on food.gov.uk
Source: FSA See Less”
Scam by Blackcass of Houston, TX or LA, CA or probably China somewhere., South Jordan, UT, USA
February 17, 2021 6:09 PM
“A scam regarding a small knock-off chain saw that is the center of a scam by Blackcass of Houston, TX or LA, CA or probably China somewhere. We ordered a Blackcass 2020 Hot selling GTA 26 Battery-Powered Wood Cutter X 1 in December 2020. We did received, via USPS, a 25" long segment of chain saw l... See Moreinks with Orange handles on each end, so it is NOT Battery-Operated. One of the photos in the Blackcass ad that are associated with this SCAM are EXACTLY the same photo used by the very legitimate Stihl company model GTA-26...only the word, "Stihl" is omitted on the Blackcass ad's photo. So, consumers and the real manufacturer are BOTH being scammed. See Less”
Blackcass.com, Fraud, Flagler Beach, Florida, USA
February 4, 2021 9:46 AM
“I ordered a hand chainsaw and only received the chain after waiting over a month. Website said it was coming from California but it came from China. They will not give me a refund. See Less”