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Power Outtage, Panola Street, New Orleans, LA, USA

2 weeks ago

Panola Street, New Orleans, 70118 Louisiana, United States

My power has been out since 3 am but my neighbors' power is on. How is that and when will the power be back on? 7700 block.

517


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Residents across Glenwood Springs reported power outages around 10:20 a.m. on Friday. According to the City of Glenwood Springs Facebook page, there is currently an Xcel electrical outage that is affecting most of Glenwood Springs.

Outage link: outagemap-xcelenergy.com
Source: postindependent.com
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Around 3,000 members on the east side of Brenham stretching to Chappell Hill were without power until around 10:30 p.m., due to what Bluebonnet Electric Cooperative said was three weather-related pole fires.

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At least 10000 PPL customers without power in Lancaster County. The outages come after heavy rain and thunderstorms rolled through the county earlier in the afternoon.

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At least 10000 PPL customers without power in Lancaster County. The outages come after heavy rain and thunderstorms rolled through the county earlier in the afternoon.

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About 2,400 reported with power in Portage County Friday afternoon

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Source: record-courier.com
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About 2,400 reported with power in Portage County Friday afternoon

Outage link: outages.firstenergycorp.com
Source: record-courier.com
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At least 10000 PPL customers without power in Lancaster County. The outages come after heavy rain and thunderstorms rolled through the county earlier in the afternoon.

Outage link: omap.prod.pplweb.com
Source: lancasteronline.com
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Around 3,000 members on the east side of Brenham stretching to Chappell Hill were without power until around 10:30 p.m., due to what Bluebonnet Electric Cooperative said was three weather-related pole fires.

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Recent Interesting Reports

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
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440


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
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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
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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
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6/6/2022, at 2323:43 to be more precise. A significant and extensive sonic boom tore through our house, woke us, terrified our dogs and causes creaking that continued for several more seconds. It is not the “sound of freedom.” It is poor and unaware flying. It is also... See More profoundly disturbing especially in these crazy times. Our dogs didn’t settle for an hour. I didn’t settle until almost 3 am. This can’t be allowed by city ordinance. Extremely disruptive. I do have it on our doorbell and on inside house camera. It was so loud, it tripped the recordings. See Less
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Plastikon Healthcare, LLC is voluntarily recalling one (1) lot of Milk of Magnesia 2400 mg/10 mL Oral Suspension, one (1) lot of Milk of Magnesia 2400 mg/30 mL Oral Suspension, eleven (11) lots of Magnesium Hydroxide 1200 mg/Aluminum Hydroxide 1200 mg/Simethicone 120 mg per 30 mL Oral... See More Suspension, and two (2) lots of Magnesium Hydroxide 2400 mg/Aluminum Hydroxide 2400 mg/Simethicone 240 mg per 30 mL Oral Suspension to the consumer level. The products are being recalled due to microbial contamination. To date, Plastikon Healthcare has not received any reports of adverse events or injuries related to this recall.

Risk Statement: Administration or use of oral drug products with microbial contamination could potentially result in increased infections that may require medical intervention. Patients with compromised immune systems, such as patients in hospitals and nursing homes, have a higher probability of developing potentially life-threatening infections after taking a contaminated product.

Product indication, lot numbers, expiration dates, and NDC information are listed in the link below. The products are packaged for institutional use and are sold to clinics and hospitals nationwide in single use cups with a foil lid. The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 7/1/2020 and 10/31/2021, who shipped to hospitals, nursing homes, and clinics nationwide. The products are private labeled for Major Pharmaceuticals.

Plastikon Healthcare is notifying its direct customers via a recall letter to arrange for return of any recalled product. Anyone with an existing inventory of the lots which are being recalled should stop use and distribution, and quarantine immediately. Return all quarantined product to the place of purchase. For clinics, hospitals, or healthcare providers that have dispensed product to patients, please notify patients regarding the recall.

Consumers with questions regarding this recall can contact Plastikon Healthcare by phone at (785) 330-7109 Monday through Friday from 9 am to 4 pm CST. 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: Plastikon Healthcare, LLC
Brand name: Plastikon Healthcare, LLC
Product recalled: Milk of Magnesia, Magnisium Hydroxide/Aluminum Hydroxide/Simethicone Oral Suspension
Reason of the recall: Due to microbial contamination
FDA Recall date: June 08, 2022

Source: fda.gov
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