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Power outage, 6111 Sly Park Road, Kelsey, CA, USA

1 week ago

6111 Sly Park Road, Kelsey, 95667 California, United States

This morning

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
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Power Outage, Atascadero, CA, USA

53 minutes from now

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

Power Outage, Creston, CA, USA

53 minutes from now

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

Power Outage, Templeton, CA, USA

53 minutes from now

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

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

Recent Interesting Reports

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
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Company name: Pfizer
Brand name: CHANTIX
Product recalled: Varenicline tablets
Reason of the recall: N-nitroso-varenicline above acceptable daily intake level
FDA Recall date: September 16, 2021
Recall details: Pfizer is voluntarily recalling all lots of Chantix 0.5 mg and 1 mg Tablets to the patient (consumer/user) level... See More due to the presence of a nitrosamine, N-nitroso-varenicline, at or above the FDA interim acceptable intake limit. As alternative suppliers have been approved in the United States, Pfizer is undertaking this precautionary measure. Long-term ingestion of N-nitroso-varenicline may be associated with a theoretical potential increased cancer risk in humans, but there is no immediate risk to patients taking this medication. Check the link below for the full list of the recalled products.

The health benefits of stopping smoking outweigh the theoretical potential cancer risk from the nitrosamine impurity in varenicline. Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time.

Chantix is a treatment to help patients quit smoking and is intended for short-term use. People who smoke cigarettes are 15 to 30 times more likely to get lung cancer than people who do not smoke.

Smoking is also associated with many other cancers, as well as with cardiovascular disease and lung disease. CHANTIX has a safety profile that has been established over 15 years of marketing authorization and through a robust clinical program. Pfizer believes the benefit/risk profile of CHANTIX remains positive. Patients currently taking Chantix should consult with their healthcare provider about alternative treatment options.

To date, Pfizer has not received reports of adverse events assessed to be related to this recall. The NDC, Lot Number, Expiration Date, and Configuration details for Chantix Tablets are indicated in Appendix A. Photos of the products can be found in Appendix B.

The products were distributed nationwide to Wholesalers and Distributors in the United States, US Virgin Islands, and Puerto Rico from May 2019 to September 2021. Pfizer places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Pfizer has notified their direct consignees by letter to arrange for return of any recalled product.

Wholesalers and Distributors with an existing inventory of Chantix tablets, should stop use and distribution and quarantine the product immediately. If you have further distributed the recalled product, please notify any accounts or additional locations which may have received the recalled product from you. Please conduct a sub-recall to those accounts and communicate this recall information immediately.

If you received free product through the Pfizer Patient Assistance Program (PAP) or the Pfizer Institutional Patient Assistance Program (IPAP), please check your stock immediately. Additionally, if you are aware of any patients to whom you dispensed the products and who still may have the product in their possession, please ask them to return the product.

As communicated by FDA, there is no immediate risk to patients taking Chantix.iv Patients who are taking this product should consult with their health care provider to determine if alternative treatments are available.

Check the full recall details on fda.gov

Source: FDA
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I was given the second dose of the vaccine and everything was very fast in the Benalcazar, there was practically no one and a side effect I only had a little pain in my arm for a day and a half | Symptoms: Soreness 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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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

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

Company name: ICU Medical, Inc.
Brand name: Hospira
Product recalled: Aminosyn II, 15%, An Amino Acid Injection, Sulfite
Reason of the recall: Presence of visible particulate matter
FDA Recall date: September 07, 2021
Recall details: ICU Medical, Inc. is voluntarily recalling one lot (2,112 units) of Aminosyn... See More II, 15%, An Amino Acid Injection, Sulfite Free intravenous (IV) solution to the hospital/user level due to the presence of visible particulate matter identified as fibers, hair, and proteinaceous material along with other particles. 

ICU Medical became aware of this issue while inspecting retain samples as part of routine process. Administration of a drug product that contains particulate matter could result in adverse events ranging from inflammation at the site of injection to more serious events that could include the formation of a blood clot obstructing the flow of blood which could lead to end-organ damage or death. 

To date, ICU Medical, Inc. has not received reports of adverse events or illnesses related to this recall. Aminosyn II, Sulfite-Free, (an amino acid injection) infused with dextrose by peripheral vein infusion is indicated as a source of nitrogen in the nutritional support of patients with adequate stores of body fat, in whom, for short periods of time, oral nutrition cannot be tolerated, is undesirable, or inadequate. 

Aminosyn II can be administered peripherally with dilute (5 to 10%) dextrose solution and I.V. fat emulsion as a source of nutritional support. This form of nutritional support can help to preserve protein and reduce the breakdown of organic or inorganic materials, such as proteins, sugars, fatty acids, etc. in stress conditions where oral intake is inadequate. Aminosyn II is also indicated for central vein infusion to prevent or reverse excreting more nitrogen than is being taken in in patients where the intestinal tract, by the oral, surgical opening into the stomach for the introduction of food or surgical procedure for a feeding tube routes cannot or should not be used and gastrointestinal absorption of protein is impaired. 

Product was distributed nationwide both by ICU Medical direct to customers and through medical distributors. The product is for human use only. ICU Medical acquired this product from Hospira, a Pfizer company; therefore, the affected product contains a Hospira NDC number and a Hospira label. The affected product lot, manufactured in the U.S. by ICU Medical in November 2020, is listed below:  

- Aminosyn® II 15% An Amino Acid Injection, Sulfite-Free. NDC: 0409-7171-17. Catalog Number: 07171-17. Lot Number: 4989094. Expiration Date: 01-Apr-2022. Configuration: Pharmacy Bulk. Package 2-liter. Flexible. Container. Manufacture Date: November 2020. Distribution Dates: January 2021 – March 2021.

ICU Medical is notifying its distributors and customers of this recall by letter and is arranging for the return of all recalled products.

Hospitals/distributors that have a product that is being recalled should stop use/further distribution and return to the place of purchase.

Customers with questions regarding this recall can call ICU Medical at 1-844-654-7780 Monday through Friday between the hours of 8 a.m. and 5 p.m. Central time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these drug products.

Check the full recall details on fda.gov

Source: FDA
See Less

18 kids sent home in one day how come we are still putting our kids at risk? Why should they be required to attend in person. I had to pick up my daughter from school because she felt ill, she told me 6 kids plus her were... See More waiting in the hallway to get in to see a nurse. When I checked her out in the sign out sheet there was 12 kids that went home... reason on paper was sick. We got a notification from two different schools in Tustin Pioneer Middle School and Loma Vista that someone got the Virus and still we have to send our kids to school!!! THIS IS INSANE! I checked out Orange County, CA cases have been rising and more are rising in children, obvious its back to school. | Symptoms: Other See Less

Some individuals are fearing maybe the vaccines contain virus

Some people are not willing to be vaccinated against the virus which sometimes may lead to the rapid spread of the virus See Less

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
See Less