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Power Outage, Sullivan Road & Sparkle Drive, Central, LA, USA

3 weeks ago

Central, 70818 Louisiana, United States

Several traffic lights are out in the Central area after a car hit a power pole in on Tuesday morning. The accident happened in the area of Sullivan Road and Sparkle Drive on Sept. 13. At least 100 Entergy customers are without power due to the accident, according to Entergy Louisiana’s outage map. All traffic lights are out on Sullivan Road between Greenwell Springs Road and Hooper Road.

Outage link: etrviewoutage.com
Source: wafb.com
Published: 2022-09-13

40


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Many Orem residents were without power Thursday afternoon, affecting 9,109 customers in Orem, UT. The cause of the outage is due to a problem with the substation.

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At least 1,559 people are still without power in South Salem after a power outage impacted more than 2,524 customers Thursday morning, according to Portland General Electric. Crews are still working on restoring power to remaining customers. The power outage was reported at 10:55 a.m. Thursday. The... See More cause of the outage is a tree knocking down a power line on the intersection of Madrona Avenue S and Croisan Scenic Way S.

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Source: statesmanjournal.com
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There will be a planned power outage for all customers in SHERIDAN, WY in the area of south Sheridan, Big Horn, Highview, Banner and Story on 10/05/2022 at 11 PM that will last approx. 6 hours.

Outage link: customer.montana-dakota.com
Source: sheridanmedia.com
Published: 2022-10-05 See Less


There will be a planned power outage for all customers in SHERIDAN, WY in the area of south Sheridan, Big Horn, Highview, Banner and Story on 10/05/2022 at 11 PM that will last approx. 6 hours.

Outage link: customer.montana-dakota.com
Source: sheridanmedia.com
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Large commercial structure fire at Bucke's Feed & Grain off of 6th Street and Railroad Avenue. The fire has reportedly knocked down nearby powerlines and has cut power to over 1,100 PG&E customers in the area.

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More than 3,500 Consumers Energy customers in northeast Genesee County will lose power overnight while crews repair a substation near Otisville. The company says power will be shut off to 3,566 customers from midnight to 2 a.m. Friday so crews can safely fix equipment in the substation.... See More The outage will occur in areas of Forest and Thetford townships bounded by Willard Road to the north, Washburn Road to the east, Genesee Road to the west and Francis Road to the south.

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Source: abc12.com
Published: 2022-10-06
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Indiana Michigan Power reported an outage near Elkhart High School Thursday afternoon that impacted hundreds of customers. At 2:30 p.m., more than 850 customers were impacted.

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According to National Grid’s website by a little after 7 a.m., about 720 customers were without power in Watertown, with another 30 out in the town of Pamelia. According to reports, the outage was caused by a sparking transformer on a utility pole at 22270 U.S. Route... See More 11.

Outage link: outagemap.ny.nationalgridus.com
Source: wwnytv.com
Published: 2022-10-07
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Recent Interesting Reports

Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This voluntary... See More recall only affects products with lot# GS046745. No other Clopidogrel or Atenolol products marketed by GSMS, Inc. are impacted. Both products are being recalled out of abundance of caution.

-Recalled products:
Product Description: Clopidogrel 75mg Tablets, 1,000 Count Bottle, GSMS NDC: 51407-032-10, Lot #: GS046745, Expiration Date: 12/2023
Product Description: Atenolol 25mg Tablets, 1,000 Count Bottle, GSMS NDC: 60429-027-10, Lot #: GS046745, Expiration Date: 12/2023

Atenolol tablets are indicated for the treatment of hypertension, to lower blood pressure. Clopidogrel is prescribed to lower the risk of having a stroke, blood clot, or serious heart problem for patients who have had heart attack, severe chest pain, or circulation problems as indicated in the product labeling. For more drug label information about clopidogrel bisulfate visit: DailyMed - CLOPIDOGREL- clopidogrel bisulfate tablet, film coated (nih.gov). For more drug label information about atenolol visit: DailyMed - ATENOLOL tablet (nih.gov)

Patients who suddenly stop taking atenolol, as would happen if clopidogrel were misplaced in the atenolol-labeled bottle, are at increased risk for ischemic (angina, myocardial infarction), hypertensive and arrhythmic adverse events relating to rapid withdrawal of beta antagonism. Further, patients who are on atenolol are frequently on concomitant anticoagulant and antiplatelet medications and would be at increased risk for bleeding if clopidogrel were added to the regimen. To date, GSMS, Inc. has not received any reports of adverse events related to the use of the products as part of this recall.

The lot under GSMS, Inc.’s voluntary recall has been primarily sold to AmerisourceBergen, and McKesson. AmerisourceBergen and McKesson are instructed to immediately stop distribution, quarantine all remaining products in their control, and return the recalled product to GSMS, Inc. They are also instructed to provide their customers, i.e., pharmacies and consumers, a copy of GSMS, Inc.’s recall notification, recall response form, and letter to consumers, patients, and caregivers.

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

In case you experienced harm from these products, 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: Golden State Medical Supply, Incorporated
Brand name: Golden State Medical Supply, Incorporated
Product recalled: Clopidogrel 75mg Tablets, Atenolol 25mg Tablets
Reason of the recall: Due to Label Mix-up
FDA Recall date: September 29, 2022

fda.gov
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466


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
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I received an empty bubble mailer approximately 4 x 6 from an online seller at 188 South Mountain House Parkway, Tracy, CA 95377. Said it was mailed from zip code 90021. Received on 9/28/2022. See Less
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GL
G...........l
I received the same package today. My package was empty as well.
Reply 1 week ago
YX
anonymous7118
I did too.
Reply 1 week ago
X6
anonymous7123
Mee too!!
1 Reply 1 week ago
DE
d.................w
Mine had a very low quality large caffeine and gasoline shirt
Reply 1 week ago
WF
w.....9
I did too on 9/29
Reply 1 week ago
H9
anonymous7127
Mine came today as well
Reply 1 week ago
LI
l.............e
I did to today.
Reply 1 week ago
KR
k..............3
I just got the same thing
Reply 1 week ago
I3
anonymous7132
Same
Reply 1 week ago
AN
a..........d
I did also
Reply 1 week ago
DA
d.........a
I received an empty package with nothing in
Reply 6 days ago
WN
anonymous7149
Same here. Empty envelope
Reply 6 days ago
UF
anonymous7156
same what is up with this? i wonder if it is a scam of some kind.
Reply 6 days ago
IA
anonymous7161
Empty envelope
Reply 5 days ago
CM
c....6
I did also today, same story, did you by any chance order anything from on facebook? I did thats why I'm asking so I'm wondering if its connected to that
Reply 5 days ago
5 days ago, I began usage of CVS Salicylic Acid Wart Removal Strips that contain 40%
salicylic acid. I have used them for about 5 days. Over the last five days around day two
I began having bouts of nausea but never attributed it to this. The... See More following day began
stomach cramps and pain. Today my left side of my back is burning deep inside
around the kidney area. I have excessive thirst not being fixed by drinking water. My
vision is blurry and I also have an awful taste in my mouth. The taste in my mouth is
exactly what the scent of these strips is. I looked up and then contacted a poison
control center and it is suggested this may be a case of Salicylic Acid poisoning from
this product. The occurrences over this short span ae far too coincidental for this to not
be the case. Upon further research it is nearly identical to a case in 2008 in which a
pediatric patient exposed to a similar product experienced similar symptomatology that
was determined to be a poisoning by this type of product. These products are not safe.
The product has been used on the left pointer finger below the middle knuckle. There is
some area of skin that has sloughed off and was bright pink earlier and is now white.
The finger itself feels off like neurologically off and partially numb currently. It has now
been 24 hours since I began this report and the symptoms are beginning to subside
slightly. It is a slow subside though. The only thing different today is my kidney does
not hurt constantly now it is off and on but much less intense and easing as time goes
on more so. The nausea has subsided. The taste however still remains in my mouth but
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stomach cramping, some nausea off and on but no longer constant, bloating, I
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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
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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
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467


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


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