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Power Outage, Farris Rd & College Ave, Conway, AR 72034, USA
2 weeks ago
Conway, 72034 Arkansas, United States
Strong storms downed trees and power lines in several areas across the state overnight. At one point Tuesday morning, over 6,000 homes were without power. Early Tuesday, power crews in Conway were busy working to remove trees that fell across several intersections, including College Avenue which is near The University Of Central Arkansas.
A power outage was reported at 5:09 p.m. near the Perkins Corner substation near the Peking Sunrise Restaurant & Lounge, with 459 New Hampshire Electric Cooperative customers affected, according to the NHEC website, and 150 Eversource customers impacted.
NHEC outage map: new-hampshire.libertyutilities.com
Eversource outage map: outagemap.eversource.com
Published: 2022 02 01
4 months ago
More than 4,000 Horry Electric Cooperative customers were without power in the Conway area. As of 3:30 p.m., Horry Electric Cooperative was reporting 4,136 people without power due to a broken circuit pole off of Highway 90. Santee Cooper also reported about 300 people affected by sporadic... outages in Conway, Surfside Beach, and the northern areas of Myrtle Beach earlier in the day.
Outage link: outages.horryelectric.com :8080/#
Published: 2022 01 03
5 months ago
1. Employees are exposed to Covid-19 virus, where employees are working in close proximity to each other without masks, barriers or proper distancing.
Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-09-24
9 months ago
The employer has not sanitized the work area, although there has been several known positive cases of COVID-19. This condition creates a hazard that exposes employees to contracting the COVID-19 virus. Location: Geek Squad work area.
Source: Osha.gov | Receipt Date: 2020-09-14
(1) A COVID-19 pandemic plan has not been developed and implemented for employees to include employee wellness checks, quarantining employees, informing employees for possible exposure to the virus, employee returning to work, social distancing, personal protective equipment, disinfecting/sanitizing, and employee training. Employees have tested positive for COVID-19... and required to return to work within ten days instead of 14 days.
Source: Osha.gov | Receipt Date: 2021-01-08
(1) A COVID-19 pandemic plan has not been developed and implemented for employees to include employee wellness checks, quarantining employees, informing employees for possible exposure to the virus, employee returning to work, social distancing, personal protective equipment, disinfecting/sanitizing, and employee training. Employees have tested positive for the... virus; and, they rushed to come back to work without test results.
Source: Osha.gov | Receipt Date: 2021-02-28
11 months ago
(1) A COVID-19 pandemic plan has not been developed and implemented for employees to include employee wellness checks, quarantining employees, informing employees for possible exposure to the virus, employee returning to work, social distancing, personal protective equipment, disinfecting/sanitizing, and employee training. Employees have tested positive for COVID-19;... and, the employer did not notify the other employees. The facility was not shut down for proper cleaning and sanitation.
Source: Osha.gov | Receipt Date: 2021-01-31
A Fire hydrant blew off causing a boil order in Pea Ridge. The Givens subdivision and addresses north, including Mariano Road are affected by the issued order.
Recent Interesting Reports
Natural Organics, Inc., is voluntarily recalling four lots of NaturesPlus Keto Living Sugar Control Capsules 90 count, because it was found to contain gluten. People who have allergies to wheat or gluten run the risk of serious or life-threatening allergic reactions if they consume these products. There... have been no reported incidents of illness or adverse reactions in connection with these products to date.
Individuals with Gluten intolerance may experience minor to severe reactions after consuming this product. This could include upset stomach, diarrhea, fatigue, skin reactions and more. It was discovered during routine testing that the product contains gluten. It was subsequently discovered that a raw material that is normally gluten free tested positive for gluten.
Gluten is a general name for the proteins found in wheat (wheatberries, durum, emmer, semolina, spelt, farina, farro, graham, KAMUT® khorasan wheat and einkorn), rye, barley, and triticale – a cross between wheat and rye.
The listed products were distributed nationwide to consumers, retail stores and to the following foreign countries: Kenya, Spain, Trinidad, United Arab Emirates, and the United Kingdom. The capsules are packaged in white jars and black caps; with labels having orange, white and black print bearing the product codes, lot numbers and “Best By” or “BBE” (Best Before End) dates are printed on the bottom of the bottle.
The lots affected are:
- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. 82004, UPC Code 097467820043, Lots 1362073, Best By 10/2025 and 1365200, Best By 10/2025
- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. Ue82004, UPC Code 097467820043, Lots 1361754, BBE 10/2025 and 1364325, BBE 10/2025
Consumers who may have purchased affected lots of NaturesPlus Keto Living Sugar Control Capsules are advised to return them to the place of purchase. No other Natural Organics, Inc. products are affected by this recall. Natural Organics, Inc. has removed all affected products within existing inventory.
This voluntary recall is announced in accord with FDA guidelines. We are initiating recall notices to our accounts and consumers who received inventory of the recalled products with instructions for returning the recalled products and for notifying their customers of the recall. Consumers with questions may contact the company Monday – Friday, from 8:00 am to 4:30pm EDT.
Company name: NATURAL ORGANICS, INC
Brand name: NaturesPlus
Product recalled: Keto Living Sugar Control Capsules
Reason of the recall: Undeclared Gluten
FDA Recall date: May 06, 2022
Alpine Fresh, Inc. of Doral, Florida is voluntarily recalling its 1 pound packages of "Hippie Organics" French Beans from lot# 313-626, because they have the potential to be contaminated with Listeria monocytogenes. The recalled "Hippie Organics 1lbs French Beans" were distributed in Whole Foods (CT, FL, GA,... IL, MD) , Aldi (FL) and LIDL (DE, GA, MD, NJ, NY, NC, PA, SC, VA) retail stores.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The product comes in a 1 pound, clear plastic package marked with lot # 313-626 on the back on a small, white label. No illnesses have been reported to date in connection with this problem. The potential for contamination was noted after routine testing by the company revealed the presence of Listeria monocytogenes in 1 pound packages of "Hippie Organics French Beans From lot # 313-626." The problem has been found to be isolated to the identified lot and the company has taken corrective actions to prevent a recurrence. Consumers who have purchased 1 pound packages of "Hippie Organics French Beans from lot #313-626" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-866-827-3362.
Company name: Alpine Fresh, Inc.
Brand name: Hippie Organics
Product recalled: French Beans
Reason of the recall: Listeria monocytogenes contamination
FDA Recall date: April 21, 2022
Foldable Car Door Step Stand Pedal - Access to Vehicle's Top Roof Both Feet Stand Pedal Ladder for Most SUV Truck Jeep Black (Fit F150), United States
3 weeks ago
A product being advertised on Amazon and across social media, a detachable step plate that attaches to the latching mechanism of a vehicle and rests in the door jamb, has the potential to cause severe injury or death, damage to vehicles, and potential harm to bystanders. It... poses a major fall risk, braces against a part of the vehicle that can be damaged easily, can cause broken bones and the chance of slamming the head against the vehicle and ground causing severe injury, laceration, impaction, and death from the fall. It is a direct threat to the elderly, children, and the average targeted consumer. Under no circumstances is this product ok to be selling at all. That spot of your car is not mean to hold that much weight under those circumstances. Repeated stress on that weakens it. It also pulls it out of alignment in small increments causing progressive worsening of stressors on the door hinges, the weather stripping and seals on the door from extra pressure along the bottom, and potential problems with the locking mechanism so that one day when you think it's locked it won't be. Or the latch decided to not properly catch and opens while driving. Not to mention the lack of propper safety measures for yourself in this instance alone. The step plate can easily rotate under the foot and become dislodged due to stress on the locking mechanism and pressure on the door jamb where it's not intended to be placed. Not all vehicles have the same door jamb construction either making this even more of a risk that it doesn't rest in the same way on all vehicle models posing even more threat to the user and the property around them plus the vehicle.
Perhaps even more concerning is at least one model mentions that "The wide platform of the pedal offers plenty of stability, enough room for nearly both feet, and can safely hold up to 400lbs." NEARLY both feet. This is even more concerning as it tells the consumer that you can't fully rest your entire self safely on the product as they intend you to. You can't prevent a fall if you can't even fully stand on the step. It also fails to address what size foot it is referring to in the first place. Foot sizes vary greatly. This product and all others like it being sold are extremely dangerous and are putting lives at risk and utilizing a part of a vehicle in a way strictly forbidden by vehicle manufacturers for the safety of the consumer. This may even void the warranty of the vehicle in some cases of damage.
For an example of one of the offending products you can see the following listing on Amazon.com
Also note in this particular version that it states it sits even higher than others like it increasing the chance and risk involved as well. The trend of these devices on social media is alarming. And the threat is great.
See the following for an example on social media: facebook.com
1 week ago
I just opened My package and the sunglasses are in many pieces broken and I wanted to wear them next week on My trip to Annapolis to see My Granddaughter Graduate the Naval Academy
It's a sexual supplement, called Captain Boss Bully Ruby 10000. My wife and I both took one each. We both started shaking horribly uncontrollably, our heads started throbbing, and we started sweating profusely. I started throwing up she didn't. Both of us had problems with our eyes.... Eyes were bloodshot red and super glassy. Don't know what's in those but it's nothing like the pink pussycat pill or the Rhino pills. | Symptoms: Nausea, Vomiting, Sweating, Shaking
3 days ago
I have had two packages that have 'gone missing' with USPS and have now had to refund customers. The packages never seem to leave NJ and both contained the same single items (a CD). The first small media mail package was sent on March 15th, 2022 -->... Departed post office in Pitman, NJ on Mar 15 --> arrived at South Jersey NJ Distribution Center March 15 @ 3:54pm --> March 19th - In transit to next facility and no updates after that. During April: spent a few calls completing the 'missing mail' forms both electronically and speaking to 'investigators' who promise to call back. When I receive call-backs it's to say that my missing mail electronic form 'wasn't fully filled out' or that 'the missing report action has not been updated' or that they are 'now pushing it forward.' No notifications from the USPS since then. My second package that I am going to have to refund the customer for was another small media mail package with CD sent April 25th 2022 --> USPS in possession from Sewell NJ --> April 25 2022 Departed Post Office Sewell NJ --> April 29 2022 "In transit, arriving late". It is now May 17th and still no package to the customer.
St. Paul, Minnesota, Fagron Inc. (“Fagron”) is voluntarily recalling two lots of SyrSpend SF Cherry to the hospital, pharmacy, and distributor level out of an abundance of caution. The affected lots are potentially contaminated with Burkholderia gladioli.
Burkholderia gladioli is an opportunistic pathogen most commonly affecting patients... with respiratory disease. Patients with compromised immune systems such as those with Cystic Fibrosis are at higher risk. Burkholderia gladioli also can cause complications after transplants. Exposure to contaminated product could lead to adverse events, which could be severe for at-risk individuals.
Fagron has received three complaints regarding an undesirable smell associated with the product. To date, Fagron has not received any reports of adverse events related to the product being recalled. Fagron sells this product for the extemporaneous compounding of prescriptions for oral dosing. The affected lots with expiration dates are listed below.
Item number: 805359
Size: 500 mL
NDC number: 51552-1123-5
Expiration date: 08/31/2024
Item number: 802496
Size: 4 L
Expiration date: 08/31/2024
Fagron has already notified its distributors and customers by phone, e-mail, and/or letter and is arranging for return of all recalled products. Hospitals, pharmacies, and distributors that possess affected product should quarantine this material and await further instructions from Fagron or Fagron’s recall coordinator. Please immediately discontinue use or distribution of the recalled product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Company name: Fagron Inc.
Brand name: Fagron
Product recalled: SyrSpend SF 500mL and 4L
Reason of the recall: Potential contamination with Burkholderia gladioli
FDA Recall date: May 02, 2022
Something is very wrong with the billing periods as well as the billing, my bill are always through the roof & when I’m paid up they’re always sending outstanding bills & when I call they always claim I’m behind & that isn’t true every month my bill... is over three hundred but my monthly usage is only one hundred so how is this even possible, I need some help here please investigate fairly & truthfully someone, I and the others who are like me thank you so much, no one is above the law & no one should be taken advantage of.
4 weeks ago
My dog has been having seizures for 2 year's w no known cause after many tests & trips to the emergency vet. He started throwing up the peanut butter dream bones, I finally found the source of his seizures & him being not well. I am outraged... that these so called treats would be on the market! After all my family is going through. After reading how many families have lost their fur babies from these poisonous, dangerous "treat"!! There is no amount of money that could give my family our time back w the worst experience for the past 2 years!!! It's literally killing him! What's wrong w you people???.!!!!