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.

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, New Albany-Condit Rd, New Albany, Ohio, USA

2 weeks ago

New Albany-Condit Road, New Albany, Ohio, United States

After thunderstorms made their way through Greater Columbus Monday night and early Tuesday morning, 2,300 customers across Greater Columbus are left in the dark.One area hit hardest by the storms locally was Main Street and Cleveland Avenue in Westerville, where 3,285 customers were without power. Other major outages include New Albany-Condit Road near New Albany, with 1,864 customers without power, 229 customers outages on Davidson Road in Hilliard and 152 customer outages near Avery Road in Hilliard.

Outage link: d6ss517do1xkp.cloudfront.net

Source: dispatch.com
Published: 2022-06-14

1.6K


Related Reports

Nearly 4,500 TEP customers are without power on Saturday, July 2.The biggest cluster of outages as of 12:30 p.m. was in Oro Valley. There were also about 1,900 customers without power near Prince and Mountain Avenue.
loc

Outage link: tep.com
Source: kold.com
Published: 2022-07-02 See Less


Nearly 4,500 TEP customers are without power on Saturday, July 2.The biggest cluster of outages as of 12:30 p.m. was in Oro Valley. There were also about 1,900 customers without power near Prince and Mountain Avenue.
loc

Outage link: tep.com
Source: kold.com
Published: 2022-07-02 See Less


About 3500 residents in Rockville and Derwood were without power this evening, after a thunderstorm passed through Montgomery County. Power restoration in progress

Outage link: pepco.com
Source: rockvillenights.com
Published: 2022-07-02 See Less


More than 10,000 customers were without power in Northern California, and Central Oregon in the Bend are. Power has been restored for many customers in the Bend area around 7:20 p.m Saturday

Outage link: pacificpower.net
Source: kdrv.com
Published: 2022-07-02 See Less


SMUD is currently responding to a power outage affecting customers in Downtown Sacramento, South Natomas, and Land Park. As of 1:08 p.m. 3,846 SMUD customers are without power.

Outage link: smud.org
Source: fox40.com
Published: 2022-07-03 See Less


SMUD is currently responding to a power outage affecting customers in Downtown Sacramento, South Natomas, and Land Park. As of 1:08 p.m. 3,846 SMUD customers are without power.

Outage link: smud.org
Source: fox40.com
Published: 2022-07-03 See Less


SMUD is currently responding to a power outage affecting customers in Downtown Sacramento, South Natomas, and Land Park. As of 1:08 p.m. 3,846 SMUD customers are without power.

Outage link: smud.org
Source: fox40.com
Published: 2022-07-03 See Less


A car crashed into a utility pole with a power line early Sunday morning leaving homes in the area without electricity for several hours in Newport News -leaving more than 1,225 homes without power.

Outage link: outagemap.dominionenergy.com
Source: dailypress.com
Published: 2022-07-03 See Less


Recent Interesting Reports

Green Pharmaceuticals Inc is voluntarily recalling lot 2373/21222 of SnoreStop NasoSpray, packaged in 0.3 FL OZ (9ml) bottles to the consumer level. FDA testing found product to contain microbial contamination identified as Providencia rettgeri. To date, Green Pharmaceuticals Inc has not received any reports of adverse events... See More related to this recalled lot.

This microorganism is rarely associated with human illness; however, in immunocompromised patients, the use of the recalled product could potentially result in severe or life-threatening adverse events such as bacteremia/sepsis, pneumonia, invasive fungal rhinosinusitis, or disseminated fungal infection. In non-immunocompromised patients, the use of the recalled product may result in infectious complications that are expected to be less severe and more readily responsive to treatment.

The product is used as a nasal spray to temporarily help stop or reduce symptoms of non-apneic snoring and is packaged in one single unit plastic bottle with a nasal pump as a delivery system. The affected SnoreStop NasoSpray lot includes the following: 2372/21222 (2373 is printed on a sticker placed on the bottom of the bottle and 21222 is on a sticker placed on the outer packaging).

The product can be identified by a clear transparent plastic box with the name SnoreStop NasoSpray. The product was distributed nationwide in health food stores and online. Green Pharmaceuticals Inc is notifying its retailers and customers by email and is arranging for return and replacement of all recalled products. Consumers and retailers that have product which is being recalled should stop using and return to place of purchase.

Consumers with questions regarding this recall can contact Green Pharmaceuticals Inc by phone at 805-388- 0600, Monday through Friday, 8 AM to 5 PM Pacific Standard Time. 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.

Company name: Green Pharmaceuticals Inc
Brand name: SnoreStop
Product recalled: Nasal spray
Reason of the recall: Due to microbial contamination identified as Providencia rettgeri.
FDA Recall date: June 09, 2022

Source: fda.gov
See Less
441


Vi-Jon, LLC is voluntarily recalling 1 (one) lot of CVS Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) to the consumer level. Testing identified the affected lot of the product to contain the bacteria Gluconacetobacter liquefaciens. This lot of Magnesium Citrate Saline... See More Laxative Oral Solution Lemon Flavor was distributed Nationwide at CVS drug store locations.

Risk Statement: Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life threatening adverse health consequences. To date, Vi-Jon, LLC has not received any complaints related to this recall. The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in 1/2 to 6 hours.

The product is packaged in a 10 oz clear round plastic bottle. The affected CVS Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor lot includes the following batch number: 0556808 and expiration date: 12/2023 on the shoulder of the bottle. This lot of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor was sent to a 3rd Party Outside Lab for testing per CVS request as a first production sample for CVS.

Vi-Jon, LLC has already notified CVS by phone and email and is arranging for return of all recalled product. Consumers that have this recalled product should stop using and return any remaining product to the place of purchase.

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

In case you experienced harm 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: Vi-Jon, LLC
Brand name: CVS Health
Product recalled: Magnesium Citrate Saline Laxative Oral Solution, Lemon Flavor
Reason of the recall: Microbial contamination with Gluconacetobacter liquefaciens
FDA Recall date: June 22, 2022

Source: fda.gov
See Less
442


There are several trees at Pinch Pond family campground that are either half or completely dead. I am concerned that with a strong storm a tree is going to fall on a camper or worse have someone in it! See Less
914


Latin Foods Market is voluntarily recalling one lot, LOTE 334 21, of Artri King Reforzado con Ortiga y Omega 3 tablets to the consumer level. FDA analysis has found the product to be tainted with diclofenac and dexamethasone. The product was distributed Nationwide in the USA, it... See More was sold online at www.latinfoods.com, and in retail stores. To date, Latin Foods Market has not received any reports of adverse events related to this recall.

Diclofenac and dexamethasone are both FDA approved drugs. Diclofenac is a non-steroidal anti-inflammatory drug (NSAID) indicated for the management of pain and arthritis and dexamethasone is a corticosteroid indicated for a variety of indications including but not limited to arthritis. The presence of diclofenac and dexamethasone in Artri King Reforzado con Ortiga y Omega 3 renders it an unapproved drug for which the safety and efficacy has not been established and, therefore, subject to recall.

Risk Statement: Consumption of undeclared diclofenac could result in serious adverse events that include cardiovascular, gastrointestinal, renal, and anaphylaxis in patients taking concomitant NSAIDs and/or anticoagulants, in those who have allergies to diclofenac, or those with underlying illnesses. Consumption of undeclared dexamethasone may lead to severe and serious adverse events such as adrenal suppression, a disorder in which the adrenal glands do not produce enough hormones, and adverse consequences can range from limited adverse consequences to death.

Artri King Reforzado con Ortiga y Omega 3 is marketed as a dietary supplement for relief of pain and inflammation associated with arthritis and osteoarthritis and is packaged in 100-count tablets per bottle within a cardboard carton, UPC 7 501031 111138. Latin Foods Market will notify all customers who ordered the product online in writing with an email instructing them to discard all recalled products after reviewing the FDA public notification link below and will post a copy of this press release on the Latin Foods Market website and in the retail stores where it was sold.

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

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: Latin Foods Market
Brand name: Arti King
Product recalled: Artri King Reforzado con Ortiga y Omega 3
Reason of the recall: Undeclared Diclofenac and Dexamethasone
FDA Recall date: June 14, 2022

Source: fda.gov
See Less
441


Price Chopper/Market 32 has issued a voluntary recall of Mount Royal Kids Citrus Foaming Hand Soap due to possible contamination with P. Aeruginosa, a microorganism found in the environment which poses a potential health risk, primarily in immunocompromised individuals.

- Mount Royal Kids Citrus Foaming Hand Soap.... See More UPC: 37432200293.

If you have the affected product, you may return it to your local store for a full refund. For more information, please check the link below or call 443-388-8485.

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.

Source: pricechopper.com
See Less
49


Hauppauge, NY, Loud Muscle Science, LLC is voluntarily recalling the following Launch Sequence products and lots listed in the table below to the consumer level. Laboratory analysis undertaken at the request of Loud Muscle Science, LLC found the products to be tainted with tadalafil, an ingredient in... See More FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The presence of tadalafil in the Launch Sequence products makes these products unapproved drugs for which the safety and efficacy have not been established and therefore, subject to recall.

Risk Statement: The most critical potential adverse health consequence of unintentional consumption of a product tainted with undeclared tadalafil is profound, life-threatening hypotension related to drug-drug interactions with nitroglycerin or guanylate cyclase inhibitors.

In the expected-use population, profound hypotension can result in a heart attack, stroke or death. To date, Loud Muscle Science has not received any reports of adverse events related to this recall. These tainted Launch Sequence Capsule products are marketed as dietary supplements for male sexual enhancement. The affected products are:

- Launch Sequence Capsules. Package Size: 60. (Bottle) ASIN: B07TLPWXDS. UPC Code: 641378938375.
- Launch Sequence Euphoria Capsules. Package Size: 10. (Tin) ASIN: B08ZJX4V9J. UPC Code: 661020846864.
- Launch Sequence Aphrodisia Capsules. Package Size: 4. (Tin) ASIN: B07QB3S2LV. UPC Code: 661020846957.
- Launch Sequence Capsules. Package Size: 60. (Bottle) ASIN: B08HM7VHCX. UPC Code: 661020848166.
- Launch Sequence Euphoria Capsules. Package Size: 10. (Tin) ASIN: B08ZJX4V9J. UPC Code: 661020846864.
- Launch Sequence Aphrodisia Capsules. Package Size: 4. (Tin) ASIN: B09S12VK3F. UPC Code: 661020846957.

The full list of lots and expiry dates is available at the link below. The Launce Sequence capsule products were sold under Amazon ASIN Nos. B07TLPWXDS (USA 60 count) and B08HM7VHCX (Canada 60 count); Launch Sequence Euphoria capsule products were sold under Amazon ASIN Nos. B08ZJX4V9J (Euphoria USA 10 count) and B08ZJX4V9J (Euphoria Canada 10 count); and Launch Sequence Aphrodisia capsule products were sold under Amazon ASIN Nos. B07QB3S2LV (Aphrodisia USA 4 count) and B09S12VK3F (Aphrodisia Canada 4 count).

The products can be identified by the labels and packaging below. The product was marketed via the Internet and fulfilled by Amazon at www.amazon.com Nationwide in the USA and www.amazon.ca in Canada, on eBay.com, and in retail stores.

Loud Muscle Science is notifying its distributors and customers by letter and this press announcement and providing a refund to its customers. Consumers that have the Launch Sequence products should stop using the product and discard.

Consumers with questions regarding this recall can contact Loud Muscle Science, LLC by phone number: 631-270-4188 -- Monday through Friday 9AM – 4PM EST. 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.

Company name: Loud Muscle Science, LLC
Brand name: Launch Sequence
Product recalled: Launch Sequence Aphrodisia and Euphoria Capsules
Reason of the recall: Contain Tadalafil
FDA Recall date: June 30, 2022

Source: fda.gov
See Less
441


Nottingham, NH, Buzzagogo Inc. is voluntarily recalling one lot of Allergy Bee Gone for Kids Nasal Swab Remedy to the consumer level due to potential microbial contamination. FDA testing found some product to contain elevated levels of yeast & mold and may contain the bacteria Bacillus cereus.... See More Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, was distributed Nationwide to wholesale distributors, retail stores and online on Amazon.com and the company web site. Buzzagogo, Inc. places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process.

Risk Statement: In immunocompromised patients, the use of the affected product could potentially result in severe or life-threatening adverse events such as bacteremia/sepsis, pneumonia, invasive fungal rhinosinusitis, or disseminated fungal infection. In non-immunocompromised patients, the population most likely to use the product, the use of the defective product may result in infectious complications, for instance bacteremia or noninvasive fungal rhinosinusitis, but in this population the infections are expected to be less severe and more readily responsive to treatment. To date, Buzzagogo, Inc. has not received any complaints related to microbial concerns or reports of adverse events related to this recalled lot.

The product is used to lessen seasonal allergy symptoms and is packaged in individual tubes for topical nasal application. The affected Allergy Bee Gone for Kids Nasal Swab Remedy lot is 2006491 with expiration date 8/2024 and UPC code 860002022116. The product can be identified by locating the lot number and expiration date on the bottom of the product carton.

Buzzagogo, Inc. is notifying its distributors and customers by email and is arranging for return or replacement of all recalled products. Consumers, distributors or retailers that have Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, should stop using the product, and discard any remaining product.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.

Company name: Buzzagogo Inc.
Brand name: Allergy Bee Gone for Kids
Product recalled: Nasal Swab Remedy
Reason of the recall: Product contains elevated levels of Bacillus cereus
FDA Recall date: June 07, 2022

Source: fda.gov
See Less
441


Received a small pkg envelope with nothing in it Sunbury, Pa. 17801 FIRST-CLASS PKG SVC June 21 2022 Mailed from zip 90021 3oz First Class pkg Size Zone 8 See Less
161


The CDC announced that they are currently investigating multistate outbreaks of Salmonella infections with serotypes Enteritidis, Hadar, Infantis, and Typhimurium.

As of June 2, 2022, 219 people infected with one of the outbreak strains have been reported from 38 states. 27 have been hospitalized. One death has... See More been reported from Tennessee. Illnesses started on dates ranging from February 15, 2022, to May 19, 2022.

State and local public health officials are interviewing people about the animals they came into contact with in the week before they got sick. Of the 87 people interviewed, 61 (70%) reported contact with backyard poultry before getting sick. Of 56 people with information available, 16 reported eating eggs from backyard poultry, and 2 reported eating meat from backyard poultry.

Backyard poultry, like chickens and ducks, can carry Salmonella germs even if they look healthy and clean. These germs can easily spread to anything in the areas where the poultry live and roam. You can get sick from touching your backyard poultry or anything in their environment and then touching your mouth or food and swallowing Salmonella germs.

CDC advises Backyard Flock Owners:
-Always wash your hands with soap and water immediately after touching backyard poultry, their eggs, or anything in the area where they live and roam.
- Use hand sanitizer if soap and water are not readily available. Consider having hand sanitizer at your coop.
- Don’t kiss or snuggle backyard poultry, and don’t eat or drink around them. This can spread Salmonella germs to your mouth and make you sick.
- Keep your backyard flock and supplies you use to care for them (like feed containers and shoes you wear in the coop) outside of the house. You should also clean the supplies outside the house.
-Don’t let children younger than 5 years touch chicks, ducklings, or other backyard poultry. Young children are more likely to get sick from germs like Salmonella.
- Collect eggs often. Eggs that sit in the nest can become dirty or break.
- Throw away cracked eggs. Germs on the shell can more easily enter the egg through a cracked shell.
- Rub off dirt on eggs with fine sandpaper, a brush, or a cloth. Don’t wash eggs because colder water can pull germs into the egg.
- Refrigerate eggs to keep them fresh and slow the growth of germs.
- Cook eggs until both the yolk and white are firm, and cook egg dishes to an internal temperature of 160°F to kill all germs.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: cdc.gov
See Less
444


CH
c...........8
syscos have poor chicken standards as well, a manager that buys it in our area said there quality has gone down hill.
Reply 1 week ago
Last 30 days