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Power outage, McFarland Boulevard East, Tuscaloosa, AL, USA

2 weeks ago

McFarland Boulevard East, Tuscaloosa, Alabama, United States

Heard a loud pop and saw a flash of light. Then no power. 3400 block.

90


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More than 1,400 Atascadero customers lost electricity Tuesday morning due to a power outage. Power went out around 10:43 a.m. Affected households were located mostly north of Highway 41 and south of Highway 46, west of Highway 101, according to PG&E.

Outage link: pgealerts.alerts.pge.com
Source: sanluisobispo.com
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The Heatherwood Drive subdivision is scheduled for a planned power outage on Wednesday from 8 a.m. to 2 p.m. The planned outage is directly related to the Heatherwood Drive Bridge Replacement Project funded under the Federal Local Bridge Program.

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A village-wide blackout left Wellington residents without power for about three hours Tuesday morning. First Energy’s only feed to the village went down around 8 a.m.

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Over 1,400 people in the Village of North Syracuse are without power Tuesday afternoon, according to National Grid. Salina has 104 people without power and Clay has 76 people without power, according to the map. A total of 1,609 people are without power in Onondaga County, according... See More to the map.

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Recent thunderstorms across Alabama have caused power outages across the state. The latest numbers from Alabama Power show that there are nearly 200 outages across the state, with nearly 8,700 customers affected.

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1. Employees are exposed to COVID-19 hazards due to employees not quarantining after a known COVID-19 close contact exposure event. 2. Employees are exposed to a COVID-19 hazard due to employees not being tested for COVID-19 after a close contact exposure event. 3. Employees are exposed to... See More a COVID-19 hazard because employees are allowed to work before a 5 day isolation period has been completed after presenting COVID-19 symptoms or a COVID-19 positive test after an exposure event. 4. Employees are exposed to a COVID-19 hazard due to employees not being required to wear face coverings in accordance with CDC guidelines after testing positive for COVID-19 or after an exposure event. 5. Employees are exposed to a COVID-19 hazard due to insufficient COVID-19 sanitation of the facility following a positive COVID-19 test result of an employee.

Alleged Hazards: 5, Employees Exposed: 80
Source: Osha.gov | Receipt Date: 2022-01-07
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We have been without power since Monday night, this is so uncomfortable having no power along with this high heat and humidity. Even had to throw out the food in the refrigerator. We don’t even have water because of a pump that takes electricity. Thank you See Less
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Pony Green (shenlantiaodong) I usually buy something on the Internet since furtanamente I fell into a scam and they don't give me a solution and they told me that this company doesn't even exist and they grab deceptive sales nothing to do with what they are selling, in fact I don't sign and don't receive anything they're selling it with See Less
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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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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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442


We fried up a fresh bag of tater tots and they exploded in our fryer! Upon further inspection of what was left in the bag,!they had flecks of green (mold? And smelled liked dirt. The expiration says 2024… I think not! See Less
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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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