Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Use camera
Select from library
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!


IMPORTANT - Your report is queued
It may take up to 12 hours to process your report.


Email us at support@safelyhq.com if you have questions.

Report by
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

If your report is poison related call 1-800-222-1222 for a free consultation with a live medical poisoning expert

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Power Outage, Berkeley Township, NJ, USA

July 9, 2021 1:46 AM

New Jersey, United States

Utility Crews and Police were on scene at Route 9 and Sylvan Lake Boulevard area for a power outage. The traffic lights on Route 9 were out. Unknown Eta for power to be restored

Source: ocscanner.news

Reported By SafelyHQ.com User
More incidents from:
Power Outage
New Jersey
United States

Related Reports

Power Outage, Lakewood Township, NJ, USA

Lakewood Township, NJ, USA

July 21, 2021 4:13 PM

“Strong thunderstorms that moved through Ocean County on Wednesday afternoon have left more than 22,000 homes without electrical service. The majority of the outages are in Lakewood, where more than 15,700 customers were without power, according to the Jersey Central Power & Light outage map. The Lakewood... See More Scoop reported a transformer fire happened in the township and the outages were causing travel delays. More than 1,700 homes in Toms River were out, and more than 2,000 in Jackson Township, according to the map.

Source: patch.com
See Less
Reported By SafelyHQ.com User

July 19, 2021 4:11 PM

“Homes and businesses serviced by the Berkeley Township MUA are being urged to boil their water after E. Coli bacteria was found.

Source: jerseyshoreonline.com See Less
Reported By SafelyHQ.com User

July 18, 2021 12:29 PM

“More than 1,200 households and businesses in the Princeton region were still without power on Sunday at 11:30 a.m. due to the Saturday storm that knocked down trees, utility poles, and power lines.

Source: planetprinceton.com See Less
Reported By SafelyHQ.com User

Power Outage, Mercer Street, Princeton, NJ, USA

Mercer Street, Princeton, NJ, USA

July 17, 2021 10:35 PM

“More than 5,000 households were without power in the Princeton region on Saturday evening due to the thunderstorm. More than 2,400 PSE&G customers in Princeton were without power, more than 2,200 PSE&G customers in Lawrence were without power, more than 1,100 customers in South Brunswick were without... See More power, and more than 900 customers in Hamilton were without power. About 165 customers in Trenton were affected, and a few dozen customers in Ewing and Pennington also lost power.

Source: planetprinceton.com
See Less
Reported By SafelyHQ.com User

July 15, 2021 4:08 PM

“Due to a power outage, as of July 13th Maplewood Township's phone lines are out of service. This outage has impacted the Maplewood Police and Fire Departments, Town Hall, and the Department of Public Works. Our technicians are working diligently to address the issue and restore service... See More as quickly as possible.

Source: twp.maplewood.nj.us
See Less
Reported By SafelyHQ.com User

Power Outage, Brick Township, NJ, USA

Brick Township, NJ, USA

July 15, 2021 3:40 PM

“Multiple signals were out in the area of Mantoloking Road, Drum Point Road, Brick Boulevard and Old Hooper Avenue. The First Energy outage map shows about a dozen scattered small power outages in the area.

Source: patch.com See Less
Reported By SafelyHQ.com User

Power Outage, Parsippany, Parsippany-Troy Hills, NJ, USA

Parsippany, Parsippany-Troy Hills, NJ, USA

July 10, 2021 2:04 PM

“Power outages in Parsippany. Jersey Central Power & Light customers were without power Wednesday morning.
The outages began around 4 a.m. mainly in northern New Jersey, with Jersey Central Power and Light and Public Service Electric and Gas Company reporting a combined 28,000 customers without power.

Source:... See More fcczv.ccbroker.it See Less
Reported By SafelyHQ.com User

Power Outage, Plainfield Avenue, Warren, NJ, USA

Plainfield Avenue, Warren, NJ, USA

July 9, 2021 6:27 AM

“A widespread power outage has hit the area overnight.

Source: tapinto.net See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, County of Union, 1143-1145 East Jersey Street, ELIZABETH, NJ, 07201, USA

County of Union, 1143-1145 East Jersey Street, ELIZABETH, NJ, 07201, USA

July 8, 2021 12:00 PM

“No social distancing and no masks

Alleged Hazards: 2, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2021-05-13 See Less
Reported By SafelyHQ.com User

July 28, 2021 7:21 PM

“The City of Campton is under a boil water advisory following an issue at the water treatment plant.

Source: wtvq.com See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

July 13, 2021 4:17 PM

“I ordered the Battery-Powered Wood Cutter, this is the second one I’ve ordered and have not received I either want my money back for 2 or I want them sent. On April 15th they shipped a Battery Powered WOOD CUTERR, I have not received it yet, plus... See More I ordered one before this, I would like to know where they are,  Aphitrite Technology limited See Less
Reported By SafelyHQ.com User

June 29, 2021 2:00 PM

“Company name: Manna Pro Products, LLC
Brand name: Flock Party
Product recalled: Duck treats
Reason of the recall: Potential to be contaminated with Salmonella
FDA Recall date: June 29, 2021
Recall details: Company Announcement Manna Pro Products, LLC, St. Louis, Missouri, is voluntarily recalling a single lot... See More of Flock Party Quack Snacks (poultry treat) with a Best By date of 12/2023, packaged in 1.68 pound bags because it has the potential to be contaminated with Salmonella.

Manna Pro Products LLC was informed by the State of West Virginia of a positive Salmonella spp. result in a routine surveillance sample of Flock Party Quack Snacks.

Salmonella is a risk 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. 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.

The bags are magenta and light blue in color and made of plastic (see images below). These products have a Best By date of 12/2023, which is printed on the bottom of the bag. This voluntary recall applies only to Flock Party Quack Snacks with Best By dates of 12/2023.

Distribution of this product has been suspended while Manna Pro continues its investigation as to the source of the contamination. This product was distributed beginning February 2, 2021 at retail stores throughout the United States.

Customers who purchased Flock Party Quack Snacks with a Best By date of 12/2023 should stop feeding the product immediately, throw the product away, and contact Manna Pro at the phone number below for a full refund. Customers with questions or concerns should contact Manna Pro at (800) 690-9908 ext. 2, Monday through Friday from 8:00 AM to 4:00 PM Central time. Members of the media can should refer their inquiries to Noah Messel of O’Malley Hansen at (314) 656-8302 or Noah.Messel@omalleyhansen.com.  

Check the full recall details on fda.gov

Source: FDA
See Less
Diagnosis: Salmonella

July 14, 2021 9:01 PM

“Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
Product recalled: Sunscreen
Reason of the recall: Testing identified low levels of benzene
FDA Recall date: July 14, 2021
Recall details: Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen... See More product lines to the consumer level. Internal testing identified low levels of benzene in some samples of the products. Consumers should stop using the affected products and follow the instructions set forth below.

The only sunscreen products impacted are aerosol products, specifically: NEUTROGENA® Beach Defense® aerosol sunscreen:
- NEUTROGENA® Cool Dry Sport aerosol sunscreen
- NEUTROGENA® Invisible Daily™ defense aerosol sunscreen
- NEUTROGENA® Ultra Sheer® aerosol sunscreen
- AVEENO® Protect + Refresh aerosol sunscreen

Benzene is classified as a human carcinogen, a substance that could potentially cause cancer depending on the level and extent of exposure. Benzene is ubiquitous in the environment. Humans around the world have daily exposures indoors and outdoors from multiple sources. Benzene can be absorbed, to varying degrees, by inhalation, through the skin, and orally. Based on exposure modeling and the Environmental Protection Agency’s (EPA) framework, daily exposure to benzene in these aerosol sunscreen products at the levels detected in our testing would not be expected to cause adverse health consequences. Out of an abundance of caution, we are recalling all lots of these specific aerosol sunscreen products.

While benzene is not an ingredient in any of our sunscreen products, it was detected in some samples of the impacted aerosol sunscreen finished products. We are investigating the cause of this issue, which is limited to certain aerosol sunscreen products. Sunscreen use is critical to public health. Melanoma incidences continue to increase worldwide, and the majority of cases are caused by excessive sun exposure. It is important that people everywhere continue to take appropriate sun protection measures, including the continued use of alternative sunscreen.

The recalled sunscreen products are packaged in aerosol cans. The products were distributed nationwide through a variety of retail channels.

Consumers should stop using these specific products and appropriately discard them.

Check the full recall details on fda.gov

Source: FDA
See Less

July 12, 2021 2:22 PM

“I ordered the hand-held battery operated chainsaw from Amphitrite Technology Limited on Facebook, but what I received was a hand-held chain. No saw was delivered. This company is a SCAM. Do not order anything from them. See Less
Reported By SafelyHQ.com User

July 13, 2021 8:00 PM

“Company name: Innoveix Pharmaceuticals, Inc.
Brand name: Innoveix Pharmaceuticals, Inc.
Product recalled: Injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg
Reason of the recall: Potential lack of sterility assurance
FDA Recall date: July 13, 2021
Recall details: Innoveix Pharmaceuticals, Inc. is voluntarily recalling the following lots... See More of sterile compounded drug products, within expiry. The products are being recalled due to a lack of assurance of sterility. These concerns arose following a routine inspection of the pharmacy by FDA.

Administration of a drug product intended to be sterile, that is not sterile, could result in serious infections which may be life-threatening. To date, Innoveix Pharmaceuticals, Inc. has not received any reports of adverse events related to this recall. This voluntary recall is being conducted out of an abundance of caution and to promote patient safety, which is the pharmacy's highest priority.

The affected products are injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg. The products can be used for various indications as prescribed. The products can be identified by an Innoveix Pharmaceuticals, Inc. label. The products were distributed in glass vials contained in a small 3 inch by 3 inch white box.

Products were distributed nationwide to both customers and/or medical facilities. A full list of the affected products with the applicable lot numbers and expiration dates is as follows:

Product Lot/Expiry
Semorelin / Ipamorelin 3mg Lot# SIP210; Exp: 12/15/2021
Lot# SIP215; Exp: 01/14/2022
Lot# SIP220; Exp: 01/23/2022

AOD-9604 3mg Lot# AOD205; Exp: 11/09/2021
Lot# AOD210; Exp: 11/18/2021
Lot# AOD 215; Exp: 12/15/2021
Lot# AOD202; Exp: 11/09/2021

Check the full recall details on fda.gov

Source: FDA
See Less

July 1, 2021 5:21 PM

“I ordered the small power handsaw for 19.99 on Facebook on May 13, 2021, and as of present day, I have not received the merchandise that I purchased. I recently been seeing the ad on fb market place for the same power handsaw, but now they are... See More asking for 14.99. Please remove these people or flag them for removal of this platform with a stiff penalty for consumer fraud. See Less
Reported By SafelyHQ.com User

July 19, 2021 9:02 PM

“Company name: Alpha Male Plus
Brand name: Alpha Male Plus
Product recalled: Alpha Male Plus Male Enhancer fruit chew
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 19, 2021
Recall details: Tucson, AZ, Alpha Male Plus is voluntarily recalling all lots within expiry of Alpha... See More Male Plus Male Enhancer fruit chews to the consumer level. FDA analysis has found the product to be tainted with tadalafil, an ingredient known as a phosphodiesterase (PDE-5) inhibitor found in a FDA approved product for the treatment of male erectile dysfunction. The presence of tadalafil in Alpha Male Plus Male Enhancer renders the product an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.

Risk Statement: Consumers with underlying medical conditions who take Alpha Male Plus Male Enhancer with undeclared tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, Alpha Male Plus has not received any reports of adverse events related to this recall.

The tainted Alpha Male Plus Male Enhancer product was manufactured by Dr Manuel Mascarenas M.D. in Tucson, Arizona located at 5190 E Farness Dr Ste 104, 85712. Dr Mascarenas is the originator and manufacturer of these products for the global market. Alpha Male Plus was selected to act as the US distributor and distribute these products for the US market.

The tadalafil ingredient was never disclosed or made known to its US distributor and was only discovered through FDA laboratory analysis. Dr Manuel Mascarenas is solely responsible for the creation, formulation and proliferation of this product. Through the use of concealment, dishonest means and an unknowing 3rd party Dr Mascarenas was able to begin distributing this mislabeled and potentially harmful product to the US market.

Alpha Male Plus was marketed as a dietary supplement for male sexual enhancement and is packaged in 1strip per foil pouch within a cardboard box, UPC [8 60003 03770 6] [8 60003 74512 0].

The affected Alpha Male Plus Male Enhancer includes all lots. The product was distributed nationwide in the USA via internet directly to consumers via their website.

Company is notifying its distributors and customers by e-mail and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using or return to place of purchase/discard/contact their doctor, etc.

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

Check the full recall details on fda.gov

Source: FDA
See Less

July 11, 2021 3:25 PM

“I saw the chain saw advertised on Facebook and ordered it 4 months ago and still have not recieved it they got my money though. And can not get a real tracking number. See Less
Reported By SafelyHQ.com User

July 23, 2021 12:03 AM

“Company name: HIS
Brand name: HIS
Product recalled: Dietary Supplement for Weight Loss
Reason of the recall: Undeclared Sibutramine
FDA Recall date: July 22, 2021
Recall details: Palisades Park, NJ, HIS is voluntarily recalling all lots and all presentations of Miss Slim (10 count & 30 count... See More capsules) to the consumer level. HIS decided to recall Miss Slim after it was contacted by the FDA regarding the presence of sibutramine in the product.

Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues. The presence of sibutramine in Miss Slim renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. To date, HIS has not received any reports of adverse events related to this recall.

The product is marketed as a dietary supplement and is packaged 10 count UPC (742137605030) and 30 count UPC (609728434472) capsules. The product sold online at missslimusa.com.

Risk Statement: Products containing sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

HIS is notifying its customers by website missslimusa.com and is arranging for return of all recalled products. Consumers that have Miss Slim which is being recalled should stop using it. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Check the full recall details on fda.gov

Source: FDA
See Less

July 19, 2021 6:51 PM

“Ordered hand chainsaw from them off Facebook. I got a weird metal string thing that I almost threw away because I nor anyone I asked knew what the hell it was. What a ripoff!!! I am trying to get my money back, but if they think for... See More one moment that I'm going to pay to have that piece of sh*t sent back to them, they better think again!! See Less
Reported By SafelyHQ.com User