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
Use camera
Select from library
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, Monroe, CT, USA

2 weeks ago

Monroe, Connecticut, United States

Nearly 400 Monroe residents and businesses were without power Thursday morning.

Source: patch.com
Source publication date: 2021 09 02

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
See Less

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

Power Outage, Creston, CA, USA

3 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

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

Recent Interesting Reports

PetSmart, in cooperation with the Consumer Product Safety Commission (CPSC), announced a voluntary recall of more than 100,000 of the Top Paw® Double Diner Dog Bowl after learning of a potential risk of laceration if the gasket on the bottom of the product comes off, leaving an... See More unfinished edge. No other products are affected by this recall.

According to CPSC, PetSmart has received three reports of consumers receiving cuts and scratches after handling the bowls with the unfinished edge.

- Top Paw® Double Diner Dog Bowl. SKU: 5270098. UPC: 73725775404

The recalled product is described as a set of two elevated metal dog food bowls that sit in a metal base surrounded by a plastic gasket. The bowls were sold at the pet stores from October 2017 through June 2021.

The company advises consumers to immediately stop using the recalled product and to the nearest PetSmart for a full refund.

Source: petsmartcorporate.com
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

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
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

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

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: Teligent Pharma, Inc.
Brand name: Teligent
Product recalled: Lidocaine HCl Topical Solution 4%
Reason of the recall: Super potency
FDA Recall date: August 30, 2021
Recall details: Teligent Pharma, Inc. is voluntarily recalling one lot of Lidocaine HCl Topical Solution 4%, 50ml in a screw... See More cap glass bottle to the user level. The product is being recalled because the firms testing has found it to be super potent based on an Out of Specification (OOS) result obtained at the 18-month stability timepoint.

Risk Statement: Use of the super potent product would result in a higher than intended lidocaine dose above that intended.  An increased lidocaine dose could lead to the development of local anesthetic systemic toxicity depending on the duration of the treatment and the specific patient.  Local anesthetic systemic toxicity can result in central nervous system reactions including excitation and/or depression and more serious signs of cardiovascular toxicity, such as bradycardia, hypotension, and even cardiovascular collapse can present very quickly.

If local anesthetic systemic toxicity is not recognized and treated quickly, severe morbidity and even death can result. Adults and the elderly who are more likely to use this product as well as children of lower body weight are more likely to experience local anesthetic systemic toxicity if a higher than intended lidocaine concentration is administered.

To date, Teligent Pharma, Inc. has not received any reports of adverse events related to this recall. The product is indicated for the production of topical anesthesia of accessible mucous membranes of the oral and nasal cavities and proximal portions of the digestive tract and is packaged in a 50ml glass bottle with a screw cap with the identification NDC# 52565-009-50.  The affected Lidocaine HCl Topical Solution 4% lot number and expiration date are:  Lot # 14218, Exp. 09/2022.  The product can be identified by the following labeling:  Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL).  

Product was distributed at the wholesale and retail distribution levels in the US and Canada. Teligent Pharma, Inc. is notifying its distributors via Fed-Ex and is arranging for return of all recalled products. Distributors, consumers, and patients that have Lidocaine HCl Topical Solution 4% which is being recalled should return product to their place of purchase.

Consumers with questions regarding this recall can contact Teligent Pharma, Inc. by phone at 1-856-697-1441 press * to reach the medical information call center Monday through Friday, 8am – 5pm. 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.

Check the full recall details on fda.gov

Source: FDA
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: 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
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