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Power Outage, Walden, TN, USA

3 weeks ago

Walden, Tennessee, United States

Wednesday night's storms have left some customers in the dark, here are the latest outage reports from local utilities as of 10:20 pm:

EBP: The utility is reporting outages in the following areas: Harrison-Hwy 58, Hamilton-Gunbarrel, Chattanooga Valley, East Chattanooga, Brainerd, Signal Mountain-Walden, Bakewell-Sale Creek, Hixson-Northgate, Soddy Daisy, Ridgedale-Main Street, Rossville-Ft. Oglethorpe and Red Bank-Moccasin.
Outage link: epb.com

NORTH GA EMC: The utility is reporting 175 outages in Catoosa, Chattooga, Floyd, Murray, Walker and Whitfield counties.
Wednesday night's storms have left some customers in the dark.
Outage link: www2.ngemc.com :81/

VEC: The utility is reporting 231 outages in Bradley, Hamilton, McMinn, Polk, Rhea counties and other areas.
Outage link: ebill.vec.org

SEQUACHEE VEC: The utility is reporting 97 power outages across Marion, Grundy and Sequatchie counties.
Outage link: outageentry.com

Source: wrcbtv.com
Published: 2021 12 29

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Recent Interesting Reports

Woody’s Pet Food Deli is recalling Raw Cornish Hen pet food “With Supplements” sticker due to a Salmonella health risk. The product was distributed in the company’s retail stores in Minneapolis, Saint Paul, and Woodbury, Minnesota.

Salmonella can affect animals eating the product and there is risk... See More to humans from handling contaminated products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

- Woody’s Pet Food Deli RAW CORNISH HEN with SUPPLEMENTS (5 lb. plastic tub). PLU Code 5230. Expiration date 11/20/22
- Woody’s Pet Food Deli RAW CORNISH HEN with SUPPLEMENTS (15 oz. plastic container). PLU Code 1652. Expiration date 11/20/22

Two (2) 5lb tubs were sold in the company’s St Paul store. Twelve (12) 15oz containers were distributed through its 3 Twin Cities, MN retail stores.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping, and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms.

Consumers exhibiting these signs after having contact with this product should contact their healthcare providers. Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

The company continues their investigation as to the source of the problem and will resume production when the problem is resolved. The recall is a result of FDA sampling due to a consumer complaint on another product, which testing revealed a sample of this product contains Salmonella.

Consumers who have these products should discontinue use and may return the unused portion to the place of purchase for a full refund. If you have recalled product in your home, clean refrigerators/freezers where the product was stored and clean and disinfect all bowls, utensils, food prep surfaces, pet bedding, toys, floors, and any other surfaces that the food or pet may have had contact with. Because animals can shed the bacteria in the feces when they have bowel movements, it’s particularly important to clean up the animal’s feces in yards or parks where people or other animals may become exposed, in addition to cleaning items in the home. Consumers should thoroughly wash their hands after handling the affected product or cleaning up potentially contaminated items and surfaces.

Company name: Woody’s Pet Food Deli
Brand name: Woody's Pet Food Deli
Product recalled: Raw Cornish Hen pet food “With Supplements”
Reason of the recall: Potential Salmonella
FDA Recall date: December 23, 2021

Check the full recall details on fda.gov

Source: FDA
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Oscor Inc. is voluntarily recalling 14 lots of Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 down to the user level. The Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 have been found to have increased risk of the hub cap and seal... See More on the proximal end of the device handle detaching during use.

RISK STATEMENT: The Destino Twist 14T Model DST1405525 & Guidestar 14F Model D141103 detachment of the hub cap and seal could lead to bleeding at the proximal end of the device and/or air embolism for the patient during intracardiac, renal or other peripheral placements procedures.

Oscor Inc. has reported two (2) Medical Device Reports to the FDA related to detachment of hub cap and seal on the proximal end of the device handle. The recall is limited to the two model numbers and lot numbers outlined above. There are no other recalls associated with this product.

PRODUCT INFORMATION: The product is steerable guiding sheath intended for the introduction of diagnostic and therapeutic devices into the human vascular, including but not limited to intracardiac, renal or other peripheral placements; it cannot be use for neural placements. The product is provided sterile, one unit per pouch / tray for details and can be identified on the printed labeling with the information below (1, 2, and 3).

The affected Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 were distributed Worldwide to distributors and hospitals from June 8, 2021 to November 30, 2021.

Recalled Product Impacted (1)

- Destino Twist 14F (DST1405525). UDI Number: 885672011123. Lot Number: PQOC13475. Expiration Date 10-01-2021. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14073. Expiration Date 11-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14072. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14071. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13834. Expiration Date 09-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13828. Expiration Date 09-01-2024. Packaging State Type: Sterile.
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- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12632. Expiration Date 07-01-2024. Packaging State Type: Sterile.
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- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12345. Expiration Date 06-01-2024. Packaging State Type: Sterile.
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Destino 14F Twist Model (2)

Product: Destino Twist 14F
GTIN (Unit): 00885672011123
Model: DST1405525
Sheath & Dilator: S55CM D73CM
French Size: 14F
Quantity: 6 Units

Guidestar 14F - Model (3)

Product: Guidestar 14F
GTIN (Unit): 00885672010911
Model: D141103
Sheath & Dilator: S71CM D89CM
French Size: 14F
Quantity: 543 Units

Company name: Oscor Inc.
Brand name: Oscor
Recalled: Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 steerable guiding sheath
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FDA Recall date: January 12, 2022

Check the full recall details on fda.gov

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- Always wash hands thoroughly with soap and water right after touching or feeding your bearded dragon and after touching or cleaning the area where it lives and roams.
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To date, Lohxa LLC has not received any reports of adverse events related to this recall.

The product is used as a natural vegetable laxative for the relief of occasional constipation and is packaged into 5 mL unit-dose cups. The product is distributed into cases of 20 cartons packaged with 24 units each, NDC: 50268-731-24. The affected Senna Syrup 8.8mg/5mL lot is AM1115S with expiration date of 01/2023. The product can be identified by the label attached.

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This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company name: Lohxa LLC
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Check the full recall details on fda.gov

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ALDI is voluntarily recalling Pure Being Cat Advent Calendars and Pure Being Dog Advent Calendars as a precautionary measure due to a potential choking hazard. After receiving a small number of customer complaints and discussion with the supplier, ALDI immediately removed the affected products from stores. The... See More affected products are:

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No other ALDI products are affected by this recall.

ALDI takes the safety and integrity of the products it sells seriously. If customers have product(s) affected by this voluntary recall, they should discard it immediately or return it to their local store for a full refund.

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