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Power Outage, Petaluma, CA, USA

2 weeks ago

Petaluma, California, United States

More than 700 Pacific, Gas & Electric Company customers in Petaluma were without power Sunday, according to the utility.

Source: pressdemocrat.com
Source publication date: 2021 08 29

Related Reports

Over 2,000 PG & E customers are out of power on Thursday morning in the Santa Cruz Mountains. According to PG & E, 2,151 customers in the Santa Cruz Mountains had a power outage between 6:50 pm Wednesday night and 7 am Thursday morning. The power outage... See More affected Lompico, Ben Lomond, and San Lorenzo Park, and continues along Highway 9 to Castle Rock State Park.

Source: californianewstimes.com
Source publication date: 2021 09 16
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According to Appalachian Power, 2,586 customers are without power in Kanawha County as of 9 p.m. Thursday.

Source: wsaz.com
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Received my first moderna shot yesterday afternoon. Last night I had Mild soreness at injection site and I felt a bit tired today. Not sure how much is vaccines related and how much is time change related. Took a nap and feel fine now. | Symptoms: Soreness See Less

The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not... See More ensure that employees are using the correct personal protective equipment, specifically wearing incorrect face shields while conducting their daily duties, T8 CCR 5199(e)(1). 2. The employer did not provide the required training in accordance with this subsection to employees with occupational exposure to aerosol transmissible pathogens (ATP), specifically the novel pathogen SARS-CoV-1 the virus which causes COVID-19, T8 CCR 5199(i).

Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-08
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1. The employer did not ensure to exclude employees with COVID-19 symptoms from the workplace until the return to work criteria has been met. T8 CCR 3205(c)(10)(A). 2. The employer did not ensure employees are wearing facial coverings properly. T8 CCR 3205(c)(7)(A).

Alleged Hazards: 2, Employees Exposed:... See More 1
Source: Osha.gov | Receipt Date: 2020-12-22
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The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not... See More ensure to exclude COVID-19 cases from the work place until the return to work criteria subsection (c)(11) has been met. Ref T8 CCR 3205(c)(10)(A). 2. The employer did not give notice to employees on their exposure to a COVID-19 positive case. Ref T8 CCR 3205(c)(3)(B)3. 3. The employer did not ensure employees are wearing facial coverings properly. Ref T8 CCR 3205(c)(7)(A). 4. The employer did not implement an effective screening procedure to screen employees for COVID-19 symptoms. Ref T8 CCR 3205(c)(2)(B). 5. The employer did not Identifying and regularly cleaning and disinfecting frequently touched surfaces and objects. Ref T8 CCR 3205(c)(8)(C). 6. The employer did not ensure that the restrooms were maintained in a sanitary condition. Ref T8 CCR 3366(b).

Alleged Hazards: 6, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-28
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TRIPART MANAGEMENT, INC. DBA: Five Guys 1. The employer did not give notice to employees on their potential exposure to a COVID-19 positive case. Ref T8CCR 3205(c)(3)(B)(3). T8CCR 3205(c)(3)(B)(3). 3205. COVID-19 Prevention (c) Written COVID-19 Prevention Program. Employers shall establish, implement, and maintain an effective, written COVID-19... See More Prevention Program, which may be integrated into the employer’s Injury and Illness Program required by section 3203, or be maintained in a separate document. The written elements of a COVID-19 Prevention Program shall include: (3) Investigating and responding to COVID-19 cases in the workplace. (B) The employer shall take the following actions when there has been a COVID-19 case at the place of employment: 3. Give notice of the potential COVID-19 exposure, within one business day, in a way that does not reveal any personal identifying information of the COVID-19 case, to the following: a. All employees who may have had COVID-19 exposure and their authorized representatives. b. Independent contractors and other employers present at the workplace during the high-risk exposure period.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-09
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Management and secretaries are not wearing mask while inside. A few employees not wearing masks outside of the office are also not wearing masks. 1. The employer did not ensure masks or other personal protective equipment are being properly used. T8 CCR 3203(a)(4)(6).

Alleged Hazards: 1, Employees... See More Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-30
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The employer did not maintain an effective Injury and Illness Prevention Program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not... See More implement physical distancing guidelines. T8 CCR 3203(a)(6). 2. The employer did not ensure its staff are provided the proper personal protective equipment, T8 CCR 3380(f)(1)(A)(B)(C). 3. The employer did not ensure that when employees exit the ladder they are protected by the use of personal fall protection, T8 CCR 1670(a). 4. The employer did not ensure that all ladders are maintained in good working order, T8 CCR 3276(e)(1). 5. The employer did not ensure that all employees are trained in the proper use of ladders, T8 CCR 3276(f).

Alleged Hazards: 5, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-27
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PG&E reports that 682 customers near the area of Lambert Lake Estates and Wards Ferry Road are without power this morning.

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

Recent Interesting Reports

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

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

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
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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: 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
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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

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

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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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

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
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