Power Outage, Mississippi, AR

February 10, 2021 12:00 PM

Arkansas, United States

Over 6,000 customers in Mississippi, Craighead, Crittenden, Phillips, and Poinsett counties in Arkansas are without power after an ice storm on Feb 11.

Source: wreg.com

February 25, 2021 12:00 PM

“A power outage occurred on Feb 24 in the South King area and impacted around 300 customers.

Source: jhnewsandguide.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on Feb 24 in the Santa Cru area and impacted around 3000 customers.

Source: kion546.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on the Feb 25 in the South and East shores of Staten Island area that lasted about three hours and impacted 2124 customers

Source: silive.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on Feb 25 in the Oglesby and Utica area.

Source: shawlocal.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on Feb 25 in the Mount Shasta area and impacted 2000 customers.

Source: mtshastanews.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on Feb 25 in the Conway area and impacted 4000 customers.

Source: kark.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on Feb 12 in the Powhatan County area.

Source: richmond.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on the Feb 25 in Castaic in the Hasley Canyon area that lasted about three hours and impacted 2732 customers

Source: signalscv.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on the Feb 25 from Mecca in Riverside County South to Bombay Beach in Imperial County and impacted 3400 customers

Source: kesq.com See Less”

February 25, 2021 12:00 PM

“A power outage occurred on the Feb 25 on Kamehameha Highway V near Pano Place in Kaunakakai on Molokai that lasted about three hours and impacted 1462 customers

Source: khon2.com 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”

February 13, 2021 3:46 PM

“I bit and bought a $30 GT A26 saw and found out after I had ordered it, that it was only a chain. I contacted the company and said I wanted to upgrade to the $60 chainsaw that was on their website and they said no problem & I would get the whole thing. I just received it and it is a completely diff... See Moreerent chainsaw and now the saw is not on their website anymore. Wondering how I can get my money back. See Less”

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. See Less”

February 22, 2021 11:20 PM

“I order the 2020 GTA-26 Battery powered wood cutter which they advertise at a price of $29.99. What arrived in the mail was a chain with two cloth handle, which I didn't order. They refuse to refund me or give me a return address. This is what i got in response to my request for a refund.

Pony... See MoreGreen （shenlantiaodong）
2021年2月22日 GMT+817:59
Dear customer,
Sorry to hear that you did not satisfy with the item you received.
If you would like to get the chainsaw, we may offer a discount for you to get the one you actually need.
We can make an exception for you with a surcharge $60, and you will get the chainsaw which costs $89.99. It's equivalent to you buying the chain for free. The chain you received before can be used as a simple tool as a free gift from us."

They are a complete scam See Less”

February 2, 2021 9:31 PM

“I am sick., My apartment has a rusting metal. Continuous everyday. I have reported to Cyber Village management and staff that there is a substance causing the metal to rust in my apartment. It is a colorless and odorless substance that rusts metal. This poisonous substance is in my food, clothes,... See Morehair shampoos and conditioners, hand and body lotions and all over my apartment. This poisonous substance is making me sick. This substance causes a dehydration. Also, this poison causes metal to RUST. The evidence of this Rust is on the following: Bathroom door frame and all metal objects in the bathroom are RUSTED Recliner is RUSTED Bedframe is RUSTED Air Vents rusted It is colorless and odorless; however, the effects are server chest congestion, cough, eye and throat irritation. It dries the air which dries my body and my nasal area. It causes server headache and chest/head congestion. It also causes muscle pain and darkens my skin. Also, I have the feelings of pins and needles on hands and feet when it is present on my furniture. I belive someone is poisoning me. This is dangerous for me as well as the community. If this is done to me, it can happen to anyone. 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”

February 21, 2021 9:27 AM

“I received the 2nd covid 19 vaccine shot from Pfizer at the Amazon site February 20th at 1:00 p.m..
I have a mildly sore right shoulder and no other symptoms. See Less”

February 19, 2021 5:13 PM

“I choose not to get the injection because as a Big Pharma trained drug rep, realized Pfizer, Moderna, and AZ were only given Emergency’ FDA approval and skipped the animal trials. The jab offers NO immunity nor does it stop transmission; it is therefore NOT a vaccine. It is nothing more than Expe... See Morerimental Biological Agent for a virus with a 99% survival rate (without any intervention. There are much saver therapeutics. He only benefit to the jab is a lessened symptom. The CDC updates the adverse events every Friday. As you can see from their last report, over 900 have already died and over 11,000 have sustained serious injuries.

The risk/return isn’t favorable. It takes about 7 yrs to develop a vaccine. This is way too soon. See Less”

February 1, 2021 4:52 PM

“Morning recieved: Arm sore. Headache. Then broke out in welt type hives from my face down to my toes. Had to go to ER for epi pen and steroids. See Less”

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 See Less”