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I was sold a recalled product, Nashville, TN, USA

3 weeks ago

Nashville, Tennessee, United States

I ordered a sex performance booster online, it was recalled due to adverse effects. I had a stroke later the same day. It is "MegMen performance booster ". Im in Nashville, the company that sold me the recalled over the counter drug is in New York. According I need help finding a lawyer to help me?

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Related Reports

The Oklahoma Medical Marijuana Authority has recalled 99 medical marijuana products after samples failed tests for mold, E. coli, yeast, and salmonella.

During OMMA’s routine inspections and reviewing of records, it discovered results not accurately reported by the testing lab. See images for the list of the... See More recalled products and Dispensaries.

The OMMA alerted growers and processors about the recall and they are required to inform dispensaries, who will inform the patients who purchased the product. Any patient in possession of a recalled product should return it to the dispensary.

In case you experience harm from marijuana products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: poncacitynow.com
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Thousands of customers are in the dark as strong wind gusts tore through North Central Wisconsin Monday. Some of the biggest power outages were in Nashville, where 948 homes were without power. 797 homes are in the dark in Rock Falls, 299 in Three Lakes, 289 in... See More Wolf River, and 363 in Merrill.

Outage link: wisconsinpublicservice.com
Source: waow.com
Published: 2022-05-09
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Downed line repaired, impacted 1900, power restored by Saturday afternoon

Outage link: map.datacapable.com
Source: tennessean.com
Published: 2022 04 23 See Less
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Boil Water Alerts for Businesses
More than 30,000 people were left without power in Middle Tennessee as of 9 p.m. Nashville Electric reported about 15,700 customers were without power while middle Tennessee Electric reported 14,821 customers were and 431 customers were without power in the Cumberland Electric Membership Corporation

Outage link: nespower.com ... See More Source: tennessean.com
Published: 2022 04 13
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NES reported they had over 3,500 people without power in Nashville on Wednesday as the wind continues to roll in.

Outage link: nespower.com
Source: wsmv.com
Published: 2022 03 30 See Less
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WEDNESDAY, 03/23/2022, 2:05 p.m. According to Wisconsin Public Service’s (WPS) outage map, 21,606 customers are affected. In some municipalities, nearly 100% of the customers in the city are affected.

The following locations have the most customers affected:
Lac du Flambeau – 1,214
Beecher – 1,141
Minocqua –... See More 1,095
Three Lakes – 1,062
Pembine – 1,008
Nashville – 996
Wabeno – 947

Outage link: wisconsinpublicservice.com

Source: wearegreenbay.com
Published: 2022 03 24
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1. Employees are exposed to COVID-19. 2. Masks are not enforced for employees working in close proximity. 3. Work areas are not being properly cleaned and disinfected against COVID-19. 4. Contact tracing is not being conducted for notifying exposed employees. 5. The employer is not enforcing proper... See More quarantining protocols.


Source: Osha.gov | Receipt Date: 2021-12-29
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1). Employees were not notified of exposure to positive COVID-19 cases within the facility.

Alleged Hazards: 1, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2022-01-06 See Less
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1. Employees are allowed to continue working while positive for COVID-19. 2. Employees are being exposed to COVID-19.

Alleged Hazards: 2, Employees Exposed: 100
Source: Osha.gov | Receipt Date: 2021-12-21 See Less
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Residents in Ridgetop, Tennessee are urged to boil their water due to it potentially being contaminated with fecal coliform or E. coli.

Source: fox17.com
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Recent Interesting Reports

Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary recall was initiated due to dissolution test failure detected during routine stability testing. No other... See More lots are impacted.

The recalled product is:
Anagrelide Capsules, USP 0.5 mg
NDC: 0172-5241-60
Lot # GD01090
Exp. Date 05/2022

Administration of this product with lower dissolution – taking longer to dissolve once ingested -- may result in decreased effectiveness or ineffectiveness of the drug to exert its platelet-reducing effect. Failed dissolution can result in a slower rate and extent of drug release leading to less anagrelide available in the body. For seriously ill patients with elevated platelet counts, less available anagrelide in the body could increase the risk of clotting (blood coagulation), and clotting or bleeding events such as a heart attack or stroke, which could be life-threatening. To date, Teva has not received any product quality complaints or adverse event reports, of this nature, for the recalled lot.

Anagrelide capsules are indicated for the treatment of patients with thrombocythemia, secondary to myeloproliferative neoplasms, to reduce the elevated platelet count and the risk of thrombosis and to ameliorate associated symptoms including thrombo-hemorrhagic events. Information about the affected lot is listed in the table below. It is packed in bottles with 100 Capsules. Teva distributed 4224 bottles nationwide from 07-30-2020 through 09-02-2020 to its wholesale, distributor and retail customers under the label for Teva Pharmaceuticals USA, Inc.

Company name: Teva Pharmaceuticals USA
Brand name: Teva
Product recalled: Anagrelide Capsules
Reason of the recall: Dissolution Test Failure
FDA Recall date: May 23, 2022

Source: fda.gov
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Had a power surge this morning with a loud pop and what sounded like something was being pulled off of our house. It was our for three hours and came back on.. now it is off again. See Less
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Last thing eaten was a sandwich at a Law Enforcement Appreciation meeting. 5/19/2022 in Englewood Fl. Next day feeling very sick, felt cold but no fever., then vomitting, heavy trembling, somewhat incoherent. | Symptoms: Vomiting, Shaking See Less
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Boil Water Alerts for Businesses
Driver completely destroyed my yard as well as my cement planter that is my property marker. They decided to use my yard as a short cut through to the main road. They took out my cement planter in the process. It had a flagged reflector so there... See More was absolutely no reason they could of not seen it there. When approaching the van, they decided to hop back into the van and sped off while destroying my yard in the process. They endangered my mothers safety when she went to approach the situation. Their reckless driving is a safety concern and could of caused my mother bodily harm See Less
363


I have had two packages that have 'gone missing' with USPS and have now had to refund customers. The packages never seem to leave NJ and both contained the same single items (a CD). The first small media mail package was sent on March 15th, 2022 -->... See More Departed post office in Pitman, NJ on Mar 15 --> arrived at South Jersey NJ Distribution Center March 15 @ 3:54pm --> March 19th - In transit to next facility and no updates after that. During April: spent a few calls completing the 'missing mail' forms both electronically and speaking to 'investigators' who promise to call back. When I receive call-backs it's to say that my missing mail electronic form 'wasn't fully filled out' or that 'the missing report action has not been updated' or that they are 'now pushing it forward.' No notifications from the USPS since then. My second package that I am going to have to refund the customer for was another small media mail package with CD sent April 25th 2022 --> USPS in possession from Sewell NJ --> April 25 2022 Departed Post Office Sewell NJ --> April 29 2022 "In transit, arriving late". It is now May 17th and still no package to the customer. See Less
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Something is very wrong with the billing periods as well as the billing, my bill are always through the roof & when I’m paid up they’re always sending outstanding bills & when I call they always claim I’m behind & that isn’t true every month my bill... See More is over three hundred but my monthly usage is only one hundred so how is this even possible, I need some help here please investigate fairly & truthfully someone, I and the others who are like me thank you so much, no one is above the law & no one should be taken advantage of. See Less
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I purchased 2 battery powered chainsaws on June 29, 2021. (The receipt is attached) What I received 6 to 8 weeks later was not what I have ordered. Both my receipts shows item description and booths says battery powered chainsaws ×2. Wheni have contacted the store they... See More kept telling me it was shipped and showed to be delivered. Picture of what I received is attached. Would you kindly explain to me if what I received is a battery powered chainsaw please let me know how to use it becaus I clearly cannot see battery or chain on it. Was all the pieces sent for it. Honestly it does not look anythin like chainsaw to me. But i do wear eyeglasses and have a disability. But still I kow what chainsaw looks like. Product from China - Hahdiy. See Less
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St. Paul, Minnesota, Fagron Inc. (“Fagron”) is voluntarily recalling two lots of SyrSpend SF Cherry to the hospital, pharmacy, and distributor level out of an abundance of caution. The affected lots are potentially contaminated with Burkholderia gladioli.

Burkholderia gladioli is an opportunistic pathogen most commonly affecting patients... See More with respiratory disease. Patients with compromised immune systems such as those with Cystic Fibrosis are at higher risk. Burkholderia gladioli also can cause complications after transplants. Exposure to contaminated product could lead to adverse events, which could be severe for at-risk individuals.

Fagron has received three complaints regarding an undesirable smell associated with the product. To date, Fagron has not received any reports of adverse events related to the product being recalled. Fagron sells this product for the extemporaneous compounding of prescriptions for oral dosing. The affected lots with expiration dates are listed below.

Affected products:
Lot: A67185
Item number: 805359
Size: 500 mL
NDC number: 51552-1123-5
Expiration date: 08/31/2024

Lot: A67186
Item number: 802496
Size: 4 L
NDC number:51551-1123-9
Expiration date: 08/31/2024

Fagron has already notified its distributors and customers by phone, e-mail, and/or letter and is arranging for return of all recalled products. Hospitals, pharmacies, and distributors that possess affected product should quarantine this material and await further instructions from Fagron or Fagron’s recall coordinator. Please immediately discontinue use or distribution of the recalled product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company name: Fagron Inc.
Brand name: Fagron
Product recalled: SyrSpend SF 500mL and 4L
Reason of the recall: Potential contamination with Burkholderia gladioli
FDA Recall date: May 02, 2022

Source: fda.gov
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