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Illness with Dream Bones, Constantine, MI 49042, USA
July 8, 2021 12:42 PM
Constantine, 49042 Michigan, United States
Symptoms: Diarrhea Fever Vomiting Bloody Stool Dehydration
Vomiting, diarrhea with bloody show, dehydration, and fever…at the vet now for immediate care.
San Antonio, TX, USA
June 6, 2021 6:15 PM
“My dog loved his mini dream bones they were his favorite treat... He began having grand mal seizures out of the blue so I stopped all treats and bones to see if that would help and took him to the vet. They could not pin point why... he was having them at the time but seemed to be improving while on an anti seizure. Decided to let him try his favorite bone after some time passed and within a short period of time my sweet boy was having another grand mal seizure. I have not given him dream bones since... He is doing better but will occasionally still has affects from the seizures.... I 100% believe the seizures were caused by the bones. So sad a product like this exists!! ”
Nashville, Arkansas, USA
June 10, 2021 2:52 PM
“The Dog had runny diarrhea after eating only two. ”
Symptoms: Diarrhea Vomiting
Fort Worth, TX, USA
June 24, 2021 3:09 PM
“Dreambones have been a favorite treat for my dogs. Normally purchased them from Walmart where they are made in China. Found some at a different store for less money but they are made in Vietnam. These made all 3 of my dogs ill..with vomiting and diarrhea. I... pray they are OK. Vet could not get them in today. ”
Hutchinson, MN, USA
June 25, 2021 8:42 AM
“He had been on rice/chicken diet for a week. I thought he was back to normal after diarrhea subsided. This was the only other item injested. Where can I send leftover bag to be tested for toxins? ”
Dreambone twist dog treats Dog very sick after giving him two if these yesterday, Springdale, AR, USA
Symptoms: Other Loss of Appetite Vomiting
Springdale, AR, USA
July 7, 2021 11:46 AM
“Yesterday I bought and gave my dog two dream one twist dog treats. A couple hours later he was acting sick. Head down, not himself. He's a very energetic blue Lacy so this is unlike him. Yesterday evening I noticed he was trying to poo but couldn't.... He refused his normal treats (not the dream bone but he gets blue buffalo bits after potty breaks) this was another red flag . My boy never turns down a treat.
All last night he was restless. It's now 10 am on the day after giving him the dream bone twists. He's still restless, can't get comfy, lays down then stands up then sits down with his head down. Won't eat, even things he normally loves. I've rubbed his belly and tried to comfort him. I let him out and walked him around a bit to try and help his bowels move along. Still nothing. He ate a bit of grass which is normal when dogs don't feel good. A bit later he started puking a massive amount and I could see alot of undigested dream bone in it. Those dream bones are the only new thing hes had and now he's really sick. I'm scared after reading about other law suites and issues regarding this product that my dog might have obstructed bowels from eating eat. I'm watching him closely and ready to take him to the vet as soon as I see if he's going to improve after puking or not. Vet visits are really expensive and if he needs surgery or declines further I'm going to raise hell. It's not okay for money hungry corporates to line their pockets while falsely advertising its products as safe knowing dam well it's killing beloved animals. My dog deserved a treat not a fight for his life. ”
Covid-19 OSHA Complaint, Michigan Milk Producers Association, 125 Depot St, Constantine, MI 49042, USA
Michigan Milk Producers Association, 125 Depot St, Constantine, MI 49042, USA
November 10, 2020 12:00 PM
“1. Numerous employees are refusing to wear masks on the grounds they have a medical condition. The employer has been made aware and has instructed employees to contact human resources to receive a face shield as an alternative to a face mask. This appears to be only... enforced or encouraged by some management. 2. The employer has posted signs informing milk haulers they are required to wear a mask, but this isn't being followed either. This is especially concerning because they are traveling between farms and plants and coming into contact with a lot of people multiple times a day. 3. Symptoms of Covid-19 are still being ignored by management unless a doctor tells you not to go to work or you have a fever over 100.4. Employees are still expected to report to work, and will be written up for calling in for headaches, diarrhea, sore throats etc.
Source: Osha.gov | Receipt Date: 2020-08-19 ”
West 5th Street, Flint, MI, USA
July 23, 2021 2:41 PM
“A power outage left a large swath of downtown Flint in the dark Friday afternoon.The power outage was reported around 1:45 p.m., according to Consumers Energy. About 500 customers lost electricity, including several businesses and government facilities north of I-69 and west of I-475. Consumers didn't immediately... have a cause for the outage. The utility estimates power will be restored by 5:45 p.m., but that time is subject to change.
Source: abc12.com ”
Grand Rapids, MI, USA
July 23, 2021 8:33 AM
“Parts of West Michigan are experiencing flood advisories and power outages Friday morning as storms roll through the area. As of 8 a.m., flood advisories are in effect for Barry, Kent, Ottawa and Muskegon counties. Currently, none of those advisories are scheduled to go past 12 p.m.... Friday. Along with the threat of floods, Kent County in particular is experiencing some large power outages. According to the Consumers Energy Outage Map, 3,749 customers were out of power in Kent County at around 8:15 a.m. A majority of those outages are located on the east side of Grand Rapids.
Source: wzzm13.com ”
Keego Harbor, MI, USA
July 20, 2021 9:26 PM
“Thousands in dark after storms sweep through Metro Detroit. DTE Energy reported nearly 47,000 outages on its website at 11 p.m., with large clusters near Farmington and Farmington Hills, North Branch in Lapeer County and Lake Orion in Oakland.
Source: detroitnews.com ”
Recent Interesting Reports
Augusta, GA, USA
July 12, 2021 2:22 PM
“I ordered the hand-held battery operated chainsaw from Amphitrite Technology Limited on Facebook, but what I received was a hand-held chain. No saw was delivered. This company is a SCAM. Do not order anything from them. ”
Purple Sage Lane, Hutto, TX, USA
July 19, 2021 6:51 PM
“Ordered hand chainsaw from them off Facebook. I got a weird metal string thing that I almost threw away because I nor anyone I asked knew what the hell it was. What a ripoff!!! I am trying to get my money back, but if they think for... one moment that I'm going to pay to have that piece of sh*t sent back to them, they better think again!! ”
Billings, Montana, USA
July 13, 2021 4:17 PM
“I ordered the Battery-Powered Wood Cutter, this is the second one I’ve ordered and have not received I either want my money back for 2 or I want them sent. On April 15th they shipped a Battery Powered WOOD CUTERR, I have not received it yet, plus... I ordered one before this, I would like to know where they are, Aphitrite Technology limited ”
July 11, 2021 3:25 PM
“I saw the chain saw advertised on Facebook and ordered it 4 months ago and still have not recieved it they got my money though. And can not get a real tracking number. ”
July 19, 2021 9:02 PM
“Company name: Alpha Male Plus
Brand name: Alpha Male Plus
Product recalled: Alpha Male Plus Male Enhancer fruit chew
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 19, 2021
Recall details: Tucson, AZ, Alpha Male Plus is voluntarily recalling all lots within expiry of Alpha... Male Plus Male Enhancer fruit chews to the consumer level. FDA analysis has found the product to be tainted with tadalafil, an ingredient known as a phosphodiesterase (PDE-5) inhibitor found in a FDA approved product for the treatment of male erectile dysfunction. The presence of tadalafil in Alpha Male Plus Male Enhancer renders the product an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Risk Statement: Consumers with underlying medical conditions who take Alpha Male Plus Male Enhancer with undeclared tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, Alpha Male Plus has not received any reports of adverse events related to this recall.
The tainted Alpha Male Plus Male Enhancer product was manufactured by Dr Manuel Mascarenas M.D. in Tucson, Arizona located at 5190 E Farness Dr Ste 104, 85712. Dr Mascarenas is the originator and manufacturer of these products for the global market. Alpha Male Plus was selected to act as the US distributor and distribute these products for the US market.
The tadalafil ingredient was never disclosed or made known to its US distributor and was only discovered through FDA laboratory analysis. Dr Manuel Mascarenas is solely responsible for the creation, formulation and proliferation of this product. Through the use of concealment, dishonest means and an unknowing 3rd party Dr Mascarenas was able to begin distributing this mislabeled and potentially harmful product to the US market.
Alpha Male Plus was marketed as a dietary supplement for male sexual enhancement and is packaged in 1strip per foil pouch within a cardboard box, UPC [8 60003 03770 6] [8 60003 74512 0].
The affected Alpha Male Plus Male Enhancer includes all lots. The product was distributed nationwide in the USA via internet directly to consumers via their website.
Company is notifying its distributors and customers by e-mail and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using or return to place of purchase/discard/contact their doctor, etc.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA ”
July 6, 2021 2:14 PM
“On 5/11/21, ordered a wood cutter for final payment of 25.99.
I received some wire contraption instead. No answer to emails sent. Scam. Do not order any products from FaceBook unless you like throwing away your money. ”
July 14, 2021 9:01 PM
“Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
Product recalled: Sunscreen
Reason of the recall: Testing identified low levels of benzene
FDA Recall date: July 14, 2021
Recall details: Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen... product lines to the consumer level. Internal testing identified low levels of benzene in some samples of the products. Consumers should stop using the affected products and follow the instructions set forth below.
The only sunscreen products impacted are aerosol products, specifically: NEUTROGENA® Beach Defense® aerosol sunscreen:
- NEUTROGENA® Cool Dry Sport aerosol sunscreen
- NEUTROGENA® Invisible Daily™ defense aerosol sunscreen
- NEUTROGENA® Ultra Sheer® aerosol sunscreen
- AVEENO® Protect + Refresh aerosol sunscreen
Benzene is classified as a human carcinogen, a substance that could potentially cause cancer depending on the level and extent of exposure. Benzene is ubiquitous in the environment. Humans around the world have daily exposures indoors and outdoors from multiple sources. Benzene can be absorbed, to varying degrees, by inhalation, through the skin, and orally. Based on exposure modeling and the Environmental Protection Agency’s (EPA) framework, daily exposure to benzene in these aerosol sunscreen products at the levels detected in our testing would not be expected to cause adverse health consequences. Out of an abundance of caution, we are recalling all lots of these specific aerosol sunscreen products.
While benzene is not an ingredient in any of our sunscreen products, it was detected in some samples of the impacted aerosol sunscreen finished products. We are investigating the cause of this issue, which is limited to certain aerosol sunscreen products. Sunscreen use is critical to public health. Melanoma incidences continue to increase worldwide, and the majority of cases are caused by excessive sun exposure. It is important that people everywhere continue to take appropriate sun protection measures, including the continued use of alternative sunscreen.
The recalled sunscreen products are packaged in aerosol cans. The products were distributed nationwide through a variety of retail channels.
Consumers should stop using these specific products and appropriately discard them.
Check the full recall details on fda.gov
Source: FDA ”
July 13, 2021 8:00 PM
“Company name: Innoveix Pharmaceuticals, Inc.
Brand name: Innoveix Pharmaceuticals, Inc.
Product recalled: Injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg
Reason of the recall: Potential lack of sterility assurance
FDA Recall date: July 13, 2021
Recall details: Innoveix Pharmaceuticals, Inc. is voluntarily recalling the following lots... of sterile compounded drug products, within expiry. The products are being recalled due to a lack of assurance of sterility. These concerns arose following a routine inspection of the pharmacy by FDA.
Administration of a drug product intended to be sterile, that is not sterile, could result in serious infections which may be life-threatening. To date, Innoveix Pharmaceuticals, Inc. has not received any reports of adverse events related to this recall. This voluntary recall is being conducted out of an abundance of caution and to promote patient safety, which is the pharmacy's highest priority.
The affected products are injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg. The products can be used for various indications as prescribed. The products can be identified by an Innoveix Pharmaceuticals, Inc. label. The products were distributed in glass vials contained in a small 3 inch by 3 inch white box.
Products were distributed nationwide to both customers and/or medical facilities. A full list of the affected products with the applicable lot numbers and expiration dates is as follows:
Semorelin / Ipamorelin 3mg Lot# SIP210; Exp: 12/15/2021
Lot# SIP215; Exp: 01/14/2022
Lot# SIP220; Exp: 01/23/2022
AOD-9604 3mg Lot# AOD205; Exp: 11/09/2021
Lot# AOD210; Exp: 11/18/2021
Lot# AOD 215; Exp: 12/15/2021
Lot# AOD202; Exp: 11/09/2021
Check the full recall details on fda.gov
Source: FDA ”
July 1, 2021 6:02 PM
“Company name: Ardil Commercial
Brand name: Limar
Product recalled: Hand sanitizer
Reason of the recall: Packaged in bottles that resemble drink containers
FDA Recall date: July 01, 2021
Recall details: Santo Domingo, Dominican Republic – Ardil Comercial is voluntarily recalling one lot of Limar Hand Sanitizer, packaged... in 4 oz bottles to the consumer level. The hand sanitizer is being recalled because it is packaged in containers that resemble water bottles.
The product poses a risk of ingestion. Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute.
To date, Ardil Comercial has not received any reports of adverse events related to this recall. The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in 4 oz bottles. under the brand Limar. The product can be identified by the bottle’s labels pictured below. The affected product lots include the following lot number: 079932-4611-05-J with the following expiration date: May 2022. Hand Sanitizer 4 oz Limar was distributed nationwide to a distributor who may have further distributed nationwide in the USA.
Ardil Comercial is notifying its distributors and customers by telephone, press release and is arranging for a replacement of all recalled products. Consumers and distributors that have the product which is being recalled should return to place of purchase. 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. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA ”
Phoenix, AZ, USA
June 28, 2021 11:46 PM
“Amphitrite Technology Limited. I'm supposed to report a scam that took place. I ordered a wireless power woodcutter and instead I got a metal chain with a ring at each. I paid for something real cheap. Big disappointment!! ”