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Power Outage, Geiger Heights, WA, USA

3 weeks ago

Geiger Heights, 99224 Washington, United States

Over 800 Avista customers in the Geiger Heights area are without power after a tree fell on a power line.

Source: khq.com
Source publication date: 2021 11 09

291


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


A "catastrophic" break in the Kalama water system Monday morning triggered a full water shutoff at the Port of Kalama and a boil notice for some city residents.

A boil notice is in effect for residents on Kalama River Road, Meeker Drive north of Nectarine Drive and... See More the North Port Industrial Area.

Source: twitter.com
Source publication date: 2021 12 06
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937


Recent Interesting Reports

I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT See Less
5.4K


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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I have been applying since the beginning of the month I went to two different appointments and every three hours the system messes up and thinks that I haven’t done my steps See Less
1.2K


Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products.

Risk Statement: Benzene is... See More 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.

To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See the link below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically the ones listed in the link below.

The products were distributed nationwide in the United States through various retailers. Consumers, distributors, and retailers that have product which is being recalled should stop using or selling these specific Odor-Eaters® spray products and dispose of them appropriately.

Company name: Odor-Eaters®, owned by Blistex Inc.
Brand name: Odor-Eaters®
Product recalled: Oder Eaters spray products
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 17, 2021

Check the full recall details on fda.gov

Source: FDA
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101


American Screening LLC of Shreveport, Louisiana is voluntarily recalling 153,336 units of Hand Sanitizer, containing 70% ethyl alcohol gel to the consumer level. The hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption.

Risk Statement: Ingesting hand sanitizer, which... See More is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute. To date, American Screening LLC has not received any reports of adverse events related to this recall.

The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in an eight-ounce bottle. The affected hand sanitizer lots include the following expiration dates of 5/21/2022 and 05/24/2022 for black-capped bottles and no lot numbers or expiration dates for clear capped bottles. The product can be identified by its shape (small water bottle), with a black flip top cap or clear cap with blue pouring spout with the weight of measure of eight (8) ounces/237mL, UPC 8 4005051579 2.

The Hand Sanitizer was sold to customers & distributors Nationwide via the internet at americanscreeningcorp.com and/or in-house sales.

Consumers & distributors that have this hand sanitizer which is being recalled should stop distribution/use and return to place of purchase or discard. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to ingesting the hand sanitizer packaged in the 8 oz. water bottle style.

Company name: American Screening LLC
Brand name: American Screening
Product recalled: Hand Sanitizer
Reason of the recall: Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption
FDA Recall date: November 19, 2021

Check the full recall details on fda.gov

Source: FDA
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102


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


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
14
1 Share


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
See Less
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