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
Add Photo/Video
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.

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)

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

Goodbye! and best wishes in your recovery

Power Outage, Gentilly Blvd & Belfort Ave, New Orleans, LA 70119, USA

1 week ago

New Orleans, 70119 Louisiana, United States

New Orleans Entergy reports over 200 residents were out of power in the Gentilly Terrace neighborhood on Tuesday night. However, power has been restored. It has been reported the reason for the power outage is because there was a downed wire.

Outage link: etrviewoutage.com
Source: wdsu.com
Published: 2022-09-14

548


Related Reports

Some Western Kenosha County residents are without power in the wake of the storm that moved through the area Sunday evening. The largest amount of We Energies customers affected are in the Paddock Lake area. That outage is affecting 273 customers. As of 8 p.m., cause of... See More the outage is officially undetermined.

Outage link: we-energies.com
Source: westofthei.com
Published: 2022-09-25
See Less
1.0K


The PECO Outage Map shows that there are 527 accounts without power in West Conshohocken. The map shows the outage centered near Apple and Matsonford on the riverside of the highways.

Outage link: peco.com
Source: morethanthecurve.com
Published: 2022-09-25 See Less
2.6K


Over 300 Entergy customers were without power after a car hit a utility pole near Siegen Lane early Monday, Sept. 26. The outage was reported around 2:48 a.m., near Briarbend Avenue.

Outage link: etrviewoutage.com
Source: wafb.com
Published: 2022-09-26 See Less
322


Appalachian Power on Monday morning reported hundreds of customer outages throughout multiple communities in Sullivan and Hawkins counties following a storm Sunday night.According to an area outage map, there are 1,239 customer outages total in Northeast Tennessee communities. Hundreds of customer outages were reported in the Willowbrook... See More Terrace communities. Multiple other outages — also due to tree contact — in the Shady View communities that were reported Sunday at 6:30 p.m. In Mount Carmel communities near Hammond Avenue, 196 customer outages were reported around 6:18 p.m. Power outages are also reported in the Chestnut Hills Drive area.

Outage link: d2oclp3li76tyy.cloudfront.net
Source: wjhl.com
Published: 2022-09-26
See Less
75


Appalachian Power on Monday morning reported hundreds of customer outages throughout multiple communities in Sullivan and Hawkins counties following a storm Sunday night.According to an area outage map, there are 1,239 customer outages total in Northeast Tennessee communities. Hundreds of customer outages were reported in the Willowbrook... See More Terrace communities. Multiple other outages — also due to tree contact — in the Shady View communities that were reported Sunday at 6:30 p.m. In Mount Carmel communities near Hammond Avenue, 196 customer outages were reported around 6:18 p.m. Power outages are also reported in the Chestnut Hills Drive area.

Outage link: d2oclp3li76tyy.cloudfront.net
Source: wjhl.com
Published: 2022-09-26
See Less
82


Appalachian Power on Monday morning reported hundreds of customer outages throughout multiple communities in Sullivan and Hawkins counties following a storm Sunday night.According to an area outage map, there are 1,239 customer outages total in Northeast Tennessee communities. Hundreds of customer outages were reported in the Willowbrook... See More Terrace communities. Multiple other outages — also due to tree contact — in the Shady View communities that were reported Sunday at 6:30 p.m. In Mount Carmel communities near Hammond Avenue, 196 customer outages were reported around 6:18 p.m. Power outages are also reported in the Chestnut Hills Drive area.

Outage link: d2oclp3li76tyy.cloudfront.net
Source: wjhl.com
Published: 2022-09-26
See Less
75


Many residents of Endicott will be without power for part of the afternoon. Endicott Municipal Light costumers that live South of North Street, East of Page Avenue, and West of Vestal Avenue will experience a power outage today, September 26th. The outage, which is due to system... See More maintenance, will begin at 2 p.m. and last approximately two hours.

Outage link: endicottny.com
Source: binghamtonhomepage.com
Published: 2022-09-26
See Less
125


Power outages affecting 1,642 PG&E customers began late Sunday night in San Luis Obispo. Electricity when out at 11:48 p.m., though the cause of the outage is unknown. The PG&E Outage Center marks neighborhoods south of Marsh and Santa Rosa Street going towards Sinsheimer Park as impacted.... See More

Outage link: pgealerts.alerts.pge.com
Source: ksby.com
Published: 2022-09-26
See Less
132


A vehicle hit a pole near a northwest Austin school early Monday morning, knocking out power to the campus and nearby neighborhood, according to Austin Energy. Crews responded at 2:30 a.m. after the pole was struck just before 1 a.m. at the corner of Amherst and Cassady... See More Drives. The utility’s outage map shows the outage is still affecting 84 customers in the area as of 9 a.m. Monday. Originally, 300 customers were without power because of the crash.

Outage link: outagemap.austinenergy.com
Source: kxan.com
Published: 2022-09-26
See Less
1.7K


Areas of Moss Bluff are under a boil advisory due to loss of pressure from a water leak. The precautionary boil advisory will affect the following areas:
Bordelon Road
Clifford Road
Coffey Road
Highway 171 from Bronco Cir to McFatter Trailer Park
Old Highway 171
Quail Ridge... See More Road
Watts Road
The boil advisory for Highway 171 will begin tomorrow, September 27 after water is turned off at 8:00 a.m. for a water main tie-in.

Source: twitter.com
Published: 2022-09-26
See Less
65


Recent Interesting Reports

I got this covid booster, and flu shot at the same time. Zero side effects so far, and I am on day 3 now. I assume by now I am in the clear. The picture says moderna, but he assured me it was the pfizer. See Less
1.7K


Salon Technologies International. Inc. is voluntarily recalling one lot of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A. Expiration 6/18/2023 to the consumer level. Firm lab testing has found the product to contain benzene. Benzene is classified as a human carcinogen. Exposure to benzene can... See More occur by inhalation, orally, and through the skin. Depending on duration and level of exposure, it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.

Salon Tech International, Inc. has not received any reports of adverse events related to this recall. The product is used to help reduce bacteria, that potentially can cause disease, when soap and water are not available. 512 bottles of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A, Expiration 6/18/2023 was distributed in the Seattle, Washington area.

Salon Technologies International. Inc. has notified its distributors by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using and return unused product to where it was obtained.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Salon Technologies International Inc.
Brand name: Antica Farmacista
Product recalled: Ocean Citron Hand Sanitizer
Reason of the recall: Product contains benzene
FDA Recall date: September 19, 2022

Source: fda.gov
See Less
1.6K


My sender sent it back there & I don’t know how to get in contact with the sender. See Less
7.1K


These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.

Royal Philips’ (NYSE: PHG; AEX: PHIA) subsidiary Philips Respironics is alerting... See More users of certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps that these devices should not be used by or near patients and their household members, caregivers and bed partners who have metallic implanted devices or metallic objects (such as metallic splinters) in the body. The magnetic headgear clips are used to attach the headgear straps to the masks, which is a method that is commonly used in the sleep therapy devices industry.

This is a voluntary notification to users of specific CPAP or Bi-Level PAP therapy masks containing such magnetic clips to inform them of the updated instructions and labeling. All users should read and follow Philips Respironics’ voluntarily updated warning and added contraindication described below. This represents a new and industry-leading practice.

Contraindication: Use of the mask is contraindicated for patients and their household members, caregivers and bed partners that may be in close vicinity to patients using the masks, that have implanted devices that may be affected by magnets, including but not limited to:
- Pacemakers
- Implantable cardioverter defibrillators (ICD)
- Neurostimulators
- Magnetic metallic implants/electrodes/valves placed in upper limbs, torso, or higher (i.e., neck and head)
- Cerebral spinal fluid (CSF) shunts (e.g., ventriculo peritoneal (VP) shunt)
- Aneurysm clips
- Embolic coils
- Intracranial aneurysm intravascular flow disruption devices
- Metallic cranial plates, screws, burr hole covers, and bone substitute devices
- Metallic splinters in the eye
- Ocular implants (e.g., glaucoma implants, retinal implants)
- Certain contact lenses with metal
- Implants to restore hearing or balance that have an implanted magnet (such as cochlear implants, implanted bone conduction hearing devices, and auditory brainstem implants)
- Magnetic denture attachments
- Metallic gastrointestinal clips
- Metallic stents (e.g., aneurysm, coronary, tracheobronchial, biliary)
- Implantable ports and pumps (e.g., insulin pumps)
- Hypoglossal nerve stimulators
- Devices labeled as MR (Magnetic Resonance) unsafe
- Magnetic metallic implants not labeled for MR or not evaluated for safety in a magnetic field

Patients should stop using the affected mask if the implant/medical device is contraindicated against the mask magnets. Patients should consult their physician immediately to determine if another mask can be used for their therapy. In the interim, switch to a non-magnetic mask if available, for continued therapy.

Patients should properly dispose of the mask that has magnets after an alternative is obtained. These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.

Warning: Magnets with a magnetic field strength of 400 mT are used in the mask. With the exception of the devices identified in the contraindication, ensure that the mask is kept at least 6 inches (approx. 15 cm) away from any other medical implants or medical devices that can be impacted by the magnetic fields to avoid possible effects from localized magnetic fields. This includes household members, caregivers, and bed partners that may be in close vicinity to patients that use the masks.

Impacted masks include: More than 17 million masks containing magnetic clips have been distributed by Philips Respironics to date. As of August 30, 2022, Philips Respironics has received 14 reports of patients suggesting that the mask magnets may have impacted their medical devices including pacemaker interference, pacemaker failure leading to replacement, need of shunt adjustment, resetting of automatic implantable cardioverter defibrillator (AICD), seizures, defibrillator shutting off periodically, arrhythmia, irregular blood pressure, change in heartbeats, and cognitive issues.

Patients may contact their Durable Medical Equipment (DME) provider, which supplied the masks affected by this notice. This voluntary medical device corrective action has been reported to the regulatory agencies in the countries where these masks are available.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Royal Philips’ subsidiary Philips Respironics
Brand name: Philips
Product recalled: Certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps
Reason of the recall: potential risk of serious injury

Source: fda.gov
See Less
463


bought product from Stuncloth, freshlook colorblend Gray contacts. Instead sending me what I ordered and PAID for I received MAXIY BROWN CONTACTS. This what I ordered AND IT WAS ALSO CONFIRMED IN THE EMAIL I RECEIVED BELOW. Items in this shipment Freshlook Colorblends Colored Contacts Lenses Non... See More Prescription (Buy 3 get 1 Free) × 2 Gray. I WANT MY MONEY BACK, OR THE PRODUCT THAT ORDERED AND PAID FOR!!!! See Less
169


A supplement called captain boss bully ruby 10000 made my eyes burn,water,skin burn, vomiting, shaking, goosebumps. One of the worst experiences of my life

I bought it at a convenience store witch was prob my first mistake. I’ve taken them before and never had any issues. It... See More was the only brand left so I have it a go 20 minutes later my fave and eyes started burning and my eyes got really red. I got home around 830 took a shower and no longer then 5 min started puking none stop. It’s been going on for 3 hrs. Dizzy, goosebumps and worst of all I’m not in the mood whatsoever now. | Symptoms: Vomiting, Shaking See Less
497


This package was delivered addresses to me, I didn’t order it but it came from an online seller at 1555 N. Chrisman Riad in Tracy, CA 95304 See Less
811


She began to have diarrhea 3 days ago after eating the first Dream bone. We didn't relate the problem. She got a second one the next day and the diarrhea continued for 3 days. Last night blood began to pour from her. Today they are trying to see where the bleeding is coming from to save her. | Symptoms: Diarrhea, Bloody Stool See Less
299


Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being stored outside... See More of labeled temperature requirements.  This notice covers the recall of Over-the-Counter Medical Devices. An earlier notice issued July 21, 2022 covered a related recall of Over-the-Counter Pharmaceutical Products. To date, Family Dollar has not received any consumer complaints or reports of illness related to this recall.  This recall is being conducted out of an abundance of caution.

- Recalled products:

900260 900260 CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT
900794 900794 LS SKYN NON LATEX LUBRICATED CONDOM 3CT
901260 901260 VERIQUICK PREGNANCY TEST 1CT
902343 902343 FIRST RESPONSE 2 CT
903409 903409 SKYN ORIGINAL NON LATEX CONDOM 12CT
903415 903415 SKYN ELITE NON LATEX CONDOM 12CT
939504 939504 VERIQUICK PREGNANCY TEST 1 CT
900752 900752 AT HOME MARIJUANA TEST STRIP
902816 902816 TROJAN ULTRA RIBBED LUBED 3CT
903756 903756 VERIQUICK PREGNANCY TEST 2 CT
999763 999763 TROJAN ULTRA THIN CONDOM LATEX 3CT
998221 998221 SKYN ELITE LARGE NON LATEX CONDOM 12CT
998869 998869 PREFERRED UTI TEST 1 CT
900265 900265 LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT
900531 900531 CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO
999009 999009 B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ
902274 902274 GS SALINE SOLUTION 12FL OZ
901443 901443 KY JELLY LUBRICANT 2 FL OZ
901960 901960 OPTI FREE REPLENISH MULTI PURPOSE 2 OZ
999801 999801 SIMPLY SALINE NASAL MIST 3.1 OZ
900457 OPTI FREE PURE MST DSINFCTNG SLTN 4FL OZ
902139 902139 DENTEMP ONE STEP .077OZ
906018 906018 FIXODENT ORG CREAM 2.4OZ
998762 998762 DRTALBOT TDDLR TTHPSTE BRSH TUTTI FRUTTI
905076 905076 CURAD STRNG WATRPRF STRIP 1IN 20CT
906312 906312 GS DENTURE CLEANSER GRN TAB 40CT
999619 999619 FIXODENT ADH CREAM ULTRA MAX HOLD 2.2OZ
999037 999037 CURAD FIRST AID KIT
903377 903377 POLIGRIP POWER MAX HOLD 2.2OZ
999417 999417 NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ
900737 900737 TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT
901239 901239 FIXODENT ORG CREAM TRAVEL .75OZ
906131 906131 POLIDENT DENTURE CLNS TAB 28CT
900334 900334 POLIGRIP ADH CREAM FREE 2.4OZ
906023 906023 GS DENTURE CLEAN OVRNT TAB 40CT
901634 901634 POLIDENT DENTURE CLEANSERS 84 CT
901777 901777 POLIDENT OVERNIGHT WHITENING TAB 28CT
906402 906402 FIXODENT ADH CREAM WITH SCOPE 2OZ
999632 999632 POLIGRIP EXTRACARE ADHESIVE CREAM 2.2OZ
900085 900085 SUPER POLIGRIP ADH CREAM .75OZ
900723 900723 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ

This recall goes to the retail store level. Not all of the products listed were sent to all stores. Family Dollar has notified its affected stores asking them to check their stock immediately and to quarantine and discontinue the sale of any affected product. Customers that may have bought affected product may return such product to the Family Dollar store where they were purchased without receipt. 

This recall does not apply to Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont, Washington, Alaska, or Hawaii as Family Dollar does not have any stores in Alaska or Hawaii and no Family Dollar stores in any of the other states received any products subject to this recall. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products.

Company name: Family Dollar
Brand name: Multiple brand names
Product recalled: Various OTC medical products
Reason of the recall: Product was stored outside of labeled temperature requirements.
FDA Recall date: September 16, 2022

Source: fda.gov
See Less
463


Last 30 days