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Power Outage, Custer, WA, USA

4 weeks ago

Custer, Washington, United States

According to Puget Sound Energy, over 2,000 customers have lost power in north Ferndale and Custer.

There’s also an outage impacting almost three hundred customers on North Lake Whatcom between Britton Road and Agate Bay.

Outage link: pse.com

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

736


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

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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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


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


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
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Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... See More no illnesses reported to date.

During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.

The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.

The full list of affected products is on the link below.

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. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.

Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements

Check the full recall details on the FDA website: fda.gov

Source: FDA
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101


Livia Global, Inc announced the recall of two lots of its liquid probiotics, LiviaOne Liquid Probiotics & BioLifePet Liquid Probiotics, due to the possibility of contamination by Pseudomonas aeruginosa, a microorganism that can cause life-threatening infection in immunocompromised individuals. These products are distributed nationwide through Amazon, wholesale,... See More and direct sales from the company’s website.

Pseudomonas aeruginosa is a microorganism found in the environment that, if ingested, can cause life-threatening infection in immunocompromised individuals. P. aeruginosa infections are generally limited to hospital settings.

This recall only affects the following products with the Lot# 001005-1 Best by: 04/2023 & LiviaOne Nasal Probiotics with Lot# 010620-1 Best by 08/2023 with the following ship dates:
- LiviaOne Daily Probiotics 2oz – UPC 030915 107112 Ship dates 04/16/2021 – 08/30/2021 (1067 units)
- LiviaOne Daily Probiotics 4oz – UPC 030915 107167 Ship dates - 07/09/2021 – 08/30/2021 (384 units)
- LiviaOne Topical Spray Probiotics 4oz – UPC 030915 107105 Ship dates 07/08/2021 – 07/30/2021 (571 units)
- LiviaOne Nasal Probiotics 1oz – UPC 030915 107198 Ship dates 04/21/2021 – 05/12/2021 (480 units)
- LiviaOne Nasal Probiotics 1 oz - UPC 030915 107198 Ship dates 07/14/2021 – 08/24/2021 (600 units)
- LiviaOne Nasal Probiotics 1 oz – Lot# 010620-1 UPC 030915 107198 Ship dates 10/27/2021 – 11/25/2021 (50 units)
- BioLifePet Probiotics for Cats – UPC 030915 107044 Ship dates 05/05/2021 – 07/26/2021 (128 units)
- BioLifePet Probiotics for Dogs – UPC 030915 107037 Ship dates 05/05/2021 – 08/25/2021 (128 units)

Lot numbers are located on the side of the bottle and on the bottom of the outer container in which the product is sold. No other lots or ship dates or any other LiviaOne products are affected by this recall.

Company name: Liva Global, Inc.
Brand name: LivaOne and BioLifePet
Product recalled: Probiotics
Reason of the recall: Pseudomonas aeruginosa
FDA Recall date: December 01, 2021

Check the full recall details on fda.gov

Source: FDA
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102
2 Shares


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


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


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