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Power Outage, Tyler Ln & Main St, Harwich, MA 02671, USA

2 weeks ago

Harwich, 02671 Massachusetts, United States

Around 7PM Thursday a transformer fire on a pole across from the Villa Roma Restaurant shut down dinner at the Italian eatery after power was knocked out in the neighborhood.

Source: capecod.com
Source publication date: 2021 11 18

46


Related Reports

As of around 10:30 p.m., more than 6,300 customers had no electricity, according to the Massachusetts Emergency Management Agency. At midnight, there were still about 4,800 customers without power. Just before 5 a.m., less than 1,000 people were without power, and that number had decreased to just... See More over 600 by 8 a.m.

Outage map: mema.mapsonline.net

Source: nbcboston.com
Source publication date: 2021 12 07
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According to Appalachian Power, at least 1,789 customers in the New River Valley and Roanoke Valley are without power as of 6:13 a.m. on Tuesday because of outages:

Floyd County: 1,117 customers due to two outage cases
Roanoke County: 611 customers due to three outage cases
Franklin... See More County: 50 customers due to two outage cases
Montgomery County: 11 customers due to two outage cases
Roanoke City: Less than five customers due to one outage case

Source: wfxrtv.com
Source publication date: 2021 12 07
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According to Appalachian Power, at least 1,789 customers in the New River Valley and Roanoke Valley are without power as of 6:13 a.m. on Tuesday because of outages:

Floyd County: 1,117 customers due to two outage cases
Roanoke County: 611 customers due to three outage cases
Franklin... See More County: 50 customers due to two outage cases
Montgomery County: 11 customers due to two outage cases
Roanoke City: Less than five customers due to one outage case

Source: wfxrtv.com
Source publication date: 2021 12 07
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Versant Power crews are responding to outages affecting about 690 customers in Washington and Hancock county.

Central Maine Power is reporting 82 outages, affecting 2,621 customers across the state.

CMP: cmpco.com
Versant Power: kubra.io

Source: wabi.tv
Source publication date: 2021 12 07 See Less


Versant Power crews are responding to outages affecting about 690 customers in Washington and Hancock county.

Central Maine Power is reporting 82 outages, affecting 2,621 customers across the state.

CMP: cmpco.com
Versant Power: kubra.io

Source: wabi.tv
Source publication date: 2021 12 07 See Less


ComEd was reporting a power outage affecting more than 970 customers Monday evening, including more than 700 in the Joliet area.

Source: patch.com
Source publication date: 2021 12 06 See Less


As of 8:30 a.m., Tuesday, a power outage has impacted the Bluebonnet-Siegen area.

According to Entergy's outage map, just over 1,4000 people are in the 70809 zip code have been affected by the outage.

Outage link: etrviewoutage.com

Source: wbrz.com
Source publication date: 2021 12 07 See Less


As of 10 a.m. Tuesday, First Energy reports that about 1,600 JCP&L customers in Hopatcong, are without power, with the expected restoration time of 6 p.m. Tuesday night.

The power outage in Hopatcong on Monday night was the result of a pole that fell on Brooklyn Mountain... See More Road because of high winds, taking power out for more than 2,000 residents.

Source: patch.com
Source publication date: 2021 12 07
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The outage area included 105 customers at 10:45 a.m., according to information on the AEP-Southwestern Electric Power Co. website, in an area that included Pine Tree Middle School, Lear Park and the REO Starplex and Event Center.

Source: news-journal.com
Source publication date: 2021 12 07 See Less


As of around 10:30 p.m., more than 6,300 customers had no electricity, according to the Massachusetts Emergency Management Agency. At midnight, there were still about 4,800 customers without power. Just before 5 a.m., less than 1,000 people were without power, and that number had decreased to just... See More over 600 by 8 a.m.

Outage map: mema.mapsonline.net

Source: nbcboston.com
Source publication date: 2021 12 07
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Recent Interesting Reports

FOR IMMEDIATE RELEASE – December 4, 2021 – Colchester, VT, Edge Pharma, LLC is voluntarily recalling all lots of all drugs compounded at Edge Pharma, LLC to the consumer level. All products are being recalled due to process issues that could lead to a lack of sterility... See More assurance for products intended to be sterile and could impact the safety and quality of non-sterile products.

Risk Statement: Administration of a drug product intended to be sterile, that is not sterile, could result in site specific infections as well as serious systemic infections which may be life- threatening. To date, Edge Pharma, LLC has not received and is not aware of any adverse events related to this recall. The products are used for a variety of indications and are packaged in Containers, IV bags, Syringes, Drop containers, Vials, Bottles, and Jars. The affected lots and expiration dates are included in the link listed below. The names and concentration of the drugs are listed in the link below.

The recall encompasses all compounded sterile and nonsterile drug products, within expiry, that were dispensed from Edge Pharma, LLC. The products subject to this recall were distributed nationwide and directly to customers and/or medical facilities. The products can be identified by the label containing the Edge Pharma, LLC name and logo. Edge Pharma, LLC is notifying its customers by email, Media and FDA alerts, and direct outreach.

Consumers and institutions that have Edge Pharma, LLC products should stop using the products immediately and may either return or discard the recalled lots. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these drug products.

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

Company name: Edge Pharma, LLC
Brand name: Edge Pharma, LLC
Product recalled: All drugs compounded at Edge Pharma, LLC
Process issues that could lead to a lack of sterility assurance for products intended to be sterile and could impact the safety and quality of non-sterile products
FDA Recall date: December 07, 2021

Check the full recall details on fda.gov

Source: FDA
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Sagent Pharmaceuticals, Inc. on November 19 announced the voluntary nationwide recall of four lots of Levetiracetam Injection, USP, to the user level. The lack of container closure integrity, found in reserve sample vials may result in a non-sterile product.

Risk Statement: Intravenous administration of a product intended... See More to be sterile that is not sterile could result in serious systemic infections which may be life-threatening. 

To date, Sagent has not received reports of any product complaints or adverse events associated with this issue. Levetiracetam Injection, USP 500 mg per 5 mL, is used in the treatment of certain types of seizures and is packaged in a 5mL single-does vial. The Levetiracetam Injection, USP, label and affected lot numbers with Expiration Dates and NDC number can be found in the table below. 

Product: Levetiracetam Injection, USP / Lot Number: B0G85VB /Expiration Date: Jun-2022 / NDC Number: 25021-780-05 / Distribution Dates: May 2021 - August 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K88VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: March 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K89VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: August 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B1G194A /Expiration Date: Jun-2023 / NDC Number: 25021-780-05 / Distribution Dates: October 2021.

The product was distributed Nationwide from March to November  2021.

Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Levetiracetam Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: November 22, 2021

Check the full recall details on fda.gov

Source: FDA
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Package was supposed to be delivered November 6, 2021.
After days of endless calls finally told it left teterboro post office November 5 but was never delivered or tracked since. See Less
5.4K


DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.

I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so... See More far today and STILL pieces of DreamBone Twist Sticks See Less
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1 Share


Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared wheat, milk, soy and/or coconut on the labels. People who have an allergy or severe sensitivity to soy, milk, wheat, or coconut run the risk of serious or life-threatening allergic reaction if... See More they consume products containing soy, milk, wheat, or coconut.

On 11/4/2021 during an FDA inspection the firm was notified that their labels failed to disclose the presence of allergens on some of their products. The recalled products were shipped between June 4, 2020 through October 1, 2021 to distributors and retailers in Alabama, California, Florida, and Texas. There have been no illnesses reported to date.

The affected products are:

Brand: Boba Origin. Product: 100% Whey Protein Isolate. Flavor: Brown Sugar Milk, Tea, Undeclared milk, & soy. Size: 1 gallon plastic jar. Lot No. 2106263. Exp. 07/2023

Brand: Etedream. Product: Etegrow ISO. Flavor: Snicker Doodle, Undeclared milk. Size: 2gallon plastic jar. Lot No. 2106002. Exp. 06/2023


Brand: RAW. Product: Vegan Protein Flavor: Peanut Butter, Undeclared coconut. Size: 1gallon plastic jar. Lot No. 2108070, 2104340, 2102018, 2012304, 2010266, 2010102, 2007037/746, 2005132. Exp. 08/2023, 04/2023, 02/2023, 12/2022, 10/2022, 10/2022, 07/2022, 05/2022

Brand: Steel. Product: Veg-Pro Flavor: Cookies & Crème, Undeclared Wheat. Size: 64 ounce plastic jar. Lot No. 2109390, 2104333, 2011260, 2104007/1041, 2105059, 2011260/994. Exp. 09/2023, 04/2023, 11/2022, 04/2023, 05/2023, 11/2022

Brand: Vital Force. Product: PureISO. Flavor: Milk Chocolate, Cocoa, Undeclared milk. Size: 1gallon plastic jar. Lot. No. 2108191. Exp. 09/2023

Brand: Vital Force. Product: PureISO. Flavor: Creamy Peanut, Butter Vanilla, Undeclared milk. Size: 1gallon plastic jar. Lot No. 2109068. Exp. 09/2023

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall.

This recall is being made with the knowledge of the Food and Drug Administration.

Company name: Nutracap Holdings, LLC
Brand name: Etedream, Vital Force, Raw, Boba Origin, Steel
Product recalled: Dietary Supplement Protein Powder
Reason of the recall: Undeclared wheat, milk, soy and/or coconut
FDA Recall date: November 09, 2021

Check the full recall details on fda.gov

Source: FDA
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5


Mountain Meadow Herbs of Somers, MT is recalling 54 bottles (total 240 capsules per bottle) of Mountain Meadow Herbs brand Candida Flush, Lot# 0120011Q. Some bottles from this Lot have become pressurized over time in storage. When opened, the product may forcefully expel air as well as... See More portions of capsules and powder. This may result in customers sustaining injuries to their hands and eyes, which may require medical attention.

Product was distributed to retailers in IN, MN, MT, NY, TN and in Ontario of Canada.
Product was sold directly to consumers in IN, KY, MN, MO, MT, NE, OH, PA, VA, and WI. The affected Candida Flush has the UPC 8 13086 01593 2, Lot #012001l Q, Exp 12/22.

No illnesses or serious injuries have been reported to date. The recall was the result of an internal investigation stemming from a customer complaint which revealed that the finished products were becoming pressurized over time.

This recall is being made with the knowledge of the U.S. Food and Drug Administration. If you have any of these products, please dispose of them immediately.

Company name: Mountain Meadow Herbs
Brand name: Mountain Meadow Herbs
Product recalled: Candida Flush
Reason of the recall: Due to exploding bottle risk
FDA Recall date: November 17, 2021

Check the full recall details on fda.gov

Source: FDA
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2


The Procter & Gamble Company (NYSE: PG) is voluntarily recalling all lots with expiry through September 2023 of specific Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products sold in the United States, and listed in the table below, to the... See More consumer level due to the presence of benzene detected.

Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Based on exposure modeling and the cancer risk assessments published by the Environmental Protection Agency (EPA) (IRIS database), daily exposure to benzene in the recalled products at the levels detected in our testing would not be expected to cause adverse health consequences. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. To date, The Procter & Gamble Company has not received any reports of adverse events related to this recall and is conducting this recall out of an abundance of caution.

The affected products are used as antiperspirants and hygiene products and are packaged in aerosol cans. See the link below for Product names and UPC codes and images for further descriptions. They are recalling all lots with expiry through September 2023 of the products listed in the link below.

Company name: The Proctor & Gamble Company
Brand name: Old Spice Secret
Product recalled: Old Spice and Secret Aerosol Sprays
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 23, 2021

Check the full recall details on fda.gov

Source: FDA
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101


FOR IMMEDIATE RELEASE – December 1, 2021 – Princeton, NJ, Sandoz Inc. (“Sandoz”) is initiating a recall of one lot (SAB06761A, Exp 04/2023) of Enoxaparin Sodium Injection, USP 40 mg/0.4 mL Single-Dose Syringes to the consumer level. A portion of lot SAB06761A experienced a temperature excursion during... See More shipment. Enoxaparin Sodium for Injection Lot SAB06761A was shipped to customers in the months of September and October 2021.

The exposure to higher temperatures may have significantly impacted the recalled product’s (lot SAB06761A) effectiveness and thus there may be reasonable probability of risk for patients with health conditions that the product is intended to treat. Such patients could be at risk for blood clots blocking blood vessels, an artery, or traveling to other tissues or organs causing pain, swelling, stroke, clots to the lung or death as a result of the underlying condition. To date, Sandoz has not received any reports of adverse events or injuries related to this recall.

The product is used for prevention of deep vein thrombosis (DVT) a condition that occurs when a blood clot forms in a deep vein, usually in the legs that can occur after surgeries or in patients with restricted mobility during illness; or prevention of complications associated with heart attacks. The product is packaged in cartons containing ten 0.4 mL syringes, NDC 0781-3246-64. Enoxaparin Sodium Injection was distributed Nationwide in the USA to wholesalers and retailers.

Product Name: Enoxaparin Sodium, Injection, USP 40mg/0.4 mL
NDC Number: 00781-3246-64
Lot Number: SAB06761A
Expiration Date: 04/2023
Date of Manufacture: 05/26/2021

Please note: this recall is specific to only one batch (SAB06761A) of Enoxaparin Sodium Injection, USP 40 mg/0.4 mL and does not apply to any other strengths of Sandoz Enoxaparin Sodium Injection, USP or to other lots of the 40 mg/0.4 mL SKU.

Any product returned that is not associated with this recall will be destroyed and no credit issued.

Company name: Sandoz, Inc.
Brand name: Sandoz
Product recalled: Enoxaparin Sodium Injection
Reason of the recall: Exposure to high temperatures may have impacted product effectiveness.
FDA Recall date: December 02, 2021

Check the full recall details on fda.gov

Source: FDA
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102


Nutrisure Ltd is recalling Naturya Hemp Protein Powder because it contains gluten, which is not mentioned on the label. This means the product is a possible health risk for anyone with an allergy or intolerance to gluten. This batch was only sold in Sainsbury’s stores.

Naturya Hemp... See More Protein Powder (100g)
Pack size: 100g
Batch code: W02135
Best before: end of March 2024
Allergens: Gluten

If you have bought the above product and have an allergy or intolerance to gluten, do not eat it. Instead, return it to the store from where it was bought for a full refund.

Company name: Nutrisure Ltd
Product recalled: Naturya Hemp Protein Powder
FSA Recall date: 11/30/2021

Check the full recall details on food.gov.uk

Source: FSA
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International Golden Foods, Inc (IGF) of Bensenville, IL is voluntarily recalling certain lot codes of the Al kanater brand tahini because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people... See More and others with weakened immune system. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The product was distributed nationwide and is sold in 16 Oz. jars. The jars are labelled “Al kanater Tahini.” Lot codes are printed on the jar. Product code, description, lot code, and UPC information are noted below.

Product Code: AT1LB
Product Description & Size: Al kanater Tahini Sesame Paste 1 lb. (454 gr)
Lot #: TT4N‐201127
UPC: 6‐92551‐00002‐0

No illnesses have been reported to-date in connection with the Al Kanater Brand Tahini.

This problem was revealed as a result of a random sampling by the Michigan Department of Agriculture.

Consumers who have purchased Al kanater Tahini with these lot codes should discontinue use and return it to the store of purchase for a full refund. Retailers that may have further distributed the recalled lot codes should share this notice with their customers.

Company name: International Golden Foods, Inc.
Brand name: Al Kanater
Product recalled: Tahini
Reason of the recall: Salmonella
FDA Recall date: November 30, 2021

Check the full recall details on fda.gov

Source: FDA
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101