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Power Outage, Porter, Texas, USA

2 days ago

Porter, 77365 Texas, United States

The tracker listed outages affecting 4,619 customers in Montgomery county at approximately 1:30 p.m. Tuesday. The area hardest hit by the outages appears to be around Grand Parkway leading into Porter, where nearly 1,400 people are without power, according to the tracker. Other areas particularly affected by outages include parts of Conroe and New Caney. There are several significant power outages along FM 1314 between Conroe and Porter as well. A few smaller power outages are dotted around Lake Conroe in Willis and Montgomery.

Outage link: etrviewoutage.com
Source: patch.com
Source publication date: 2021 09 14

Related Reports

According to National Grid, there are currently 941 customers affected by a power outage in Cohoes

Source: news10.com
Source publication date: 2021 09 17 See Less

2,317 customers lost power between W. Highlands BLVD to W. S Street and NW 25th to NW 4th Street. They have restored power to 1,301 customers in the areas of NW 12th to NW 14th, W. Cornhusker to Oregon Trail and 91, NW 24th to NW 12th,... See More and Superior Street to W. Cornhusker HWY.

Source: klkntv.com
Source publication date: 2021 09 17
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Springfield City Utilities is reporting that several people are without power in central Springfield.

According to the CU outage map, areas affected include:
- A big area around Glenstone and Division
- The area around Drury University and Ozarks Technical Community College
- The area around Glenstone... See More and Walnut

Outage link: myaccount.cityutilities.net

Source: ozarksfirst.com
Source publication date: 2021 09 17
See Less

Three large outages in north San Luis Obispo County have left 4,116 PG&E customers without power Friday morning, as lengthy outages have become daily occurrence in rural areas.

The lights went out in parts of Atascadero and Creston for 1,696 PG&E customers at 6:35 a.m.

Shortly after... See More 9 a.m., more than 1,000 PG&E customers lost power from Templeton to Lake Nacimiento

At 6:36 a.m., 1,417 PG&E customers in parts of Santa Margarita, Atascadero, Creston and Pozo lost power. As of 11:30 a.m., 926 of the customers remain without power, according to PG&E.

Source: calcoastnews.com
Source publication date: 2021 09 17
See Less

Three large outages in north San Luis Obispo County have left 4,116 PG&E customers without power Friday morning, as lengthy outages have become daily occurrence in rural areas.

The lights went out in parts of Atascadero and Creston for 1,696 PG&E customers at 6:35 a.m.

Shortly after... See More 9 a.m., more than 1,000 PG&E customers lost power from Templeton to Lake Nacimiento

At 6:36 a.m., 1,417 PG&E customers in parts of Santa Margarita, Atascadero, Creston and Pozo lost power. As of 11:30 a.m., 926 of the customers remain without power, according to PG&E.

Source: calcoastnews.com
Source publication date: 2021 09 17
See Less

Three large outages in north San Luis Obispo County have left 4,116 PG&E customers without power Friday morning, as lengthy outages have become daily occurrence in rural areas.

The lights went out in parts of Atascadero and Creston for 1,696 PG&E customers at 6:35 a.m.

Shortly after... See More 9 a.m., more than 1,000 PG&E customers lost power from Templeton to Lake Nacimiento

At 6:36 a.m., 1,417 PG&E customers in parts of Santa Margarita, Atascadero, Creston and Pozo lost power. As of 11:30 a.m., 926 of the customers remain without power, according to PG&E.

Source: calcoastnews.com
Source publication date: 2021 09 17
See Less

Three large outages in north San Luis Obispo County have left 4,116 PG&E customers without power Friday morning, as lengthy outages have become daily occurrence in rural areas.

The lights went out in parts of Atascadero and Creston for 1,696 PG&E customers at 6:35 a.m.

Shortly after... See More 9 a.m., more than 1,000 PG&E customers lost power from Templeton to Lake Nacimiento

At 6:36 a.m., 1,417 PG&E customers in parts of Santa Margarita, Atascadero, Creston and Pozo lost power. As of 11:30 a.m., 926 of the customers remain without power, according to PG&E.

Source: calcoastnews.com
Source publication date: 2021 09 17
See Less

More than 3,000 San Diego County residents lost power due to an unplanned outage late Friday morning, according to San Diego Gas & Electric.

Affected communities included Rancho Santa Fe, Encinitas, Cardiff and the Lake Hodges area.

Outage link: sdge.com

Source: fox5sandiego.com
Source publication date: 2021 09... See More 17 See Less

More than 3,000 San Diego County residents lost power due to an unplanned outage late Friday morning, according to San Diego Gas & Electric.

Affected communities included Rancho Santa Fe, Encinitas, Cardiff and the Lake Hodges area.

Outage link: sdge.com

Source: fox5sandiego.com
Source publication date: 2021 09... See More 17 See Less

A power outage has left thousands of people in Texoma without power for hours.

When the issue first began, around 4,500 customers were affected. Hours later, there were still around 2,900 without power.

Outage link: swre.ebill.coop

Source: texomashomepage.com
Source publication date: 2021 09 16 See Less

Recent Interesting Reports

Company name: Cardinal Health
Brand name: Monoject
Product recalled: Flush Prefilled Saline Syringes
Reason of the recall: Products have been found to reintroduce air into the syringe after the air has been expelled
FDA Recall date: August 20, 2021
Recall details: On August 4, 2021, Cardinal Health... See More (NYSE: CAH) initiated a nationwide recall of approximately 267 million MonojectTM Flush Prefilled Saline Syringes (0.9% Sodium Chloride). The products have been found to reintroduce air into the syringe after the air has been expelled. This could result in injection of air into blood vessels and create the potential for air embolism, which can cause serious adverse health outcomes or death.

Customers who have affected product(s) should immediately review their inventory and quarantine and return all affected product. The recall applies to all lots of the products manufactured from July 2019 to June 2021 distributed between July 2019 and July 2021. The following SKUs have been recalled:

- 12mL Syringe, 10 mL Saline Fill. SKUs: 8881570121
- 12mL Syringe, 3 mL Saline Fill. SKUs: 8881570123
- 12mL Syringe, 5 mL Saline Fill. SKUs: 8881570125

Our Monoject™ 3mL syringe, 2.5mL Saline Fill is not affected by this recall. This item, SKU 8881570300, will be available for sale until inventory is depleted.

MonojectTM Flush Prefilled Saline Syringes can be identified by the barrel of the syringe, the case and the box as shown in the pictures below.

The company has received 37 reports of the plunger pulling back. No injuries have been reported to date. Cardinal Health voluntarily recalled MonojectTM Flush Prefilled Saline Syringes after learning that there is potential for the syringe’s plunger to draw back and reintroduce air back into the syringe. Cardinal Health has notified the U.S. Food and Drug Administration of this action.

Cardinal Health notified its distributors and customers by overnight delivery of a notification packet on August 5, 2021 and is arranging for return of all recalled products.

Given the limited number of alternative prefilled saline syringe options, combined with ongoing supply, transportation and labor challenges, we anticipate that this recall may contribute to a market disruption of prefilled saline syringes.

Cardinal Health distributes this product nationwide.

Check the full recall details on fda.gov

Source: FDA
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Company name: Azurity Pharmaceuticals, Inc.
Brand name: Azurity
Product recalled: Firvanq
Reason of the recall: Product kit may contain incorrect diluent.
FDA Recall date: September 08, 2021
Recall details: Wilmington, MA, Azurity Pharmaceuticals, Inc. (“Azurity”) is voluntarily recalling one lot of Firvanq® (vancomycin hydrochloride for oral solution),... See More Vancomycin 50 mg/mL Kit (“Firvanq®”) to the consumer level, as some products in the affected lot have been found to incorrectly contain a First Omeprazole (FIRST-PPI) diluent instead of the Firvanq diluent bottle. To date, Azurity has not received any reports of adverse events related to this recall.

Risk Statement: Vancomycin may not be completely solubilized in the FIRST-PPI diluent which could lead to doses above or below those recommended in the label. There is reasonable probability that the administration of inappropriate doses of oral vancomycin may lead to persistent diarrhea associated with dehydration and electrolyte abnormalities, recurrence of Clostridium difficile (C. difficile) infection, its progression to severe colitis, colon perforation requiring colectomy, and potentially death. Especially, the elderly and immunocompromised patients are vulnerable to the complications of C. difficile infection.

Firvanq® is indicated for use in adults and pediatric patients less than 18 years of age for the treatment of: Clostridium difficile-associated diarrhea and Enterocolitis caused by Staphylococcus aureus (including methicillin-resistant strains).

The recalled product is packaged as a kit consisting of a bottle with Vancomycin Hydrochloride, USP powder, a bottle of Grape-Flavored diluent, and Full Prescribing Information. The product NDC is 65628-206-05 and the UPC code is 3 65628 206005 1. A total of 2,751 kits of the affected Firvanq®, lot number 21035, with an expiration date of 2022-07-31 were distributed. The product can be identified by its brand name Firvanq®.

This product was distributed nationwide through wholesale distributors. Azurity is notifying its distributors and customers by direct notifications to distributors and via this press release. Azurity is arranging for return and replacement of only recalled products. Consumers, distributors, and retailers that are in possession of Firvanq® from the affected lot should immediately stop using it and return it to the place of purchase. Distributors are asked to place any affected product under quarantine and return it promptly to Azurity.

Check the full recall details on fda.gov

Source: FDA
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A boiled water advisory surrounds our street while at the same time we experience very low water pressure especially on higher floors. See Less

I saw an ad on the internet for a mini chainsaw called rosespros.
I paid $25.99 for it in May.
They took my money but I've never recieved the saw.

I'm so tired of being scammed by these crooked companies that float around on the internet and... See More basically steal from people. I ordered from an ad that popped up when I was playing a game See Less

I ordered a wood cutter, chain saw, rechargeable on 3/18/21.  The linked showed up on Facebook.  I did not receive my chain saw.  Apparently the company, Amphitrite Technology Limited has been scamming people all year.  It wasn’t until I found your website that I realized I had... See More been sent this weird chain, hand cutter.  There are many pictures posted on your site of the same product.  I had no idea why this thing came to me.  I did not think it was a “replacement” or substitute for the little chain saw that was rechargeable.   

I can see there are several posts about the same problem. What can be done? Why has PayPal continued to allow the seller to sell? What can you do? What can I do, to stop others from the company”s fraud?

I purchased through PayPal; directly after this purchase my bank notified me that someone tried to buy a cell phone. What happens next? With so many reports of fraud, why hasn’t the seller been reported to officials? What can you do? What can I do on my part? I contacted PayPal. The company should be blocked from selling
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Company name: Top Quality Dog Food
Brand name: Top Quality Dog Food.com
Product recalled: Beef HVM
Reason of the recall: Potential Salmonella & Listeria monocytogenes contamination
FDA Recall date: August 26, 2021
Recall details: Top Quality Dog Food of Hyattsville, MD is recalling “Beef HVM” 1-pound packages... See More due to the potential of Salmonella spp., Listeria monocytogenes. Salmonella, Listeria, can affect animals eating the product and there is risk to humans handling contaminated products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping, and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever, and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. Listeria monocytogenes can cause serious and sometimes fatal infections in young children, vulnerable or elderly people, and others with compromised immune systems. Healthy people may suffer short-term symptoms such as fever, headaches, stiffness, abdominal pain, and diarrhea. Listeria monocytogenes infections pose a serious threat to pregnant woman, as it can lead to miscarriages and stillbirths. Listeria monocytogenes infections are uncommon in pets, but they are possible. Symptoms may include mild to severe diarrhea; anorexia; fever; nervous, muscular, and respiratory signs; abortion; depression; shock; and death. Healthy people should monitor themselves and their pets for symptoms.

The recalled “Beef HVM” was distributed in DC, MD, VA, DE, PA, MA, CT, and SC and product was distributed through mail order and direct delivery from 7/27/21 to 8/2/21. The “Beef HVM” comes in a 1-pound package marked with lot #071521 on the bottom right corner of the label.

No illnesses have been reported to date in connection with the “Beef HVM” 1-pound packages in question.

The contamination was noted after a state surveillance sample revealed the presence of Salmonella, Listeria monocytogenes, in some 1-pound. packages of Beef HVM. The remaining “Beef HVM” batch in our possession has been quarantined and we have discontinued the distribution of this batch while FDA and our company continue their investigation as to the source of the contamination. 

We encourage all customers who received this product to dispose of any unused product immediately. If you find the “Beef HVM” 1-pound package that shows the lot number: 071521 in your possession, we urge you to return it to the place of purchase for a full refund.

Check the full recall details on fda.gov

Source: FDA
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Scam Hahdi, CT, USA

2 weeks ago

I ordered the battery powered chain saw on May 9th and still have not received it. I would like my money back. Hahdiy
Not sure being it was so long ago See Less

Bought a bag of heartland farms dog food from our local dollar store on 7-26-21, a week later we noticed that all 3 of our dogs had bloody stool, not long after that our youngest boxer started vomiting up blood. Called our local vet explained what was... See More going on and she said to stop feeding them for 24 hours and give them pepto bismol and switch them back to pedigree immediately. All the dogs are fine now as far as I can tell. What led me to voice my concern is a gentleman down the road lost 6 puppies two weeks after buying a bag of heartland food. I am in no way seeking anything. But there is definitely something wrong with the food. Thank you. | Symptoms: Vomiting, Bloody Stool See Less

The FSAI announced the recall of unauthorized novel CBD food supplements due to the presence of unsafe levels of delta‐9‐tetrahydrocannabinol (THC) based on the European Food Safety Authority (EFSA) acute reference dose.

The recalled products are:
- Jacob Hooy, 2.75%CBD+, 10 ml, Batch number: 060977-0302, Best before... See More date: Feb-2022.
- Greenway, CBD Hemp Oil, 10 ml, Batch number: CB60001, Best before date: 10/12/2022.
- The Hemp Company, CBD Oil Original, 10 ml, Batch number: 10-10-139, Best before date: 04/2022.

FSAI requested to distributors withdraw the product from the market, and Retailers remove the products from sale. Consumers should not purchase or consume any of the implicated batches of the unauthorized novel CBD food supplements.

For more recall details check on FSAI website: fsai.ie

Source: FSAI
See Less

The FSAI announced the recall of Aptonia sports food products by Decathlon due to the presence of the unauthorized pesticide ethylene oxide. Ethylene oxide is a pesticide that is not permitted for use in foods sold in the EU but is approved for use by other countries... See More outside the EU.

The recalled products are:
- Aptonia Vitamins and Minerals 30 tablets Orange flavour
- Aptonia salts caps 100 capsules
- Aptonia Electrolytes tablets Ecosize lemon flavour 2x20 tablets
- Aptonia Electrolytes tablets rasperry flavour 2x20 tablets
- Aptonia Electrolytes tablets lemon flavour 2x20 tablets

Although the consumption of the contaminated product does not pose an acute risk to health, there is an increased risk if there is continued consumption of contaminated food over a long period of time. Therefore, exposure to this substance needs to be minimized.

In case you are experiencing food poisoning symptoms, 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.

For more recall details check on FSAI website: fsai.ie

Source: FSAI
See Less