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DreamBone Twist Sticks are making my dogs vomiT - from Chewy.com., Hickory Valley, TN, USA

2 weeks ago

Hickory Valley, 38042 Tennessee, United States

DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.

I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so far today and STILL pieces of DreamBone Twist Sticks

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1 Share


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Dream bones, the ones that are the dream bone twists with Jerry. Both times I gave my dog one of these bones he had vomiting, terrible diarrhea and lethargy. He ended up at the emergency vet since we were out of town. He's been eating dream bones... See More peanut butter flavor with no issue but the twists with jerky made him horribly ill

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WB
anonymous2446
My boy is 12 and having a bad reaction from the dream bones. I've taken him to the vet and he's on medication for the vomiting and diarrhea. But still having small runs and reddish in color. I did get him to eat some boiled chicken and hes drinking alot. Apache is a 12 year old double dappled dachshund. I will never give him any treats again and I feel horrible that I'm the reason that he's sick and may not make it.
Reply 3 weeks ago
Gave my dog a DreamBone treat and within and hour he started seizing. He had never had a seizure ever! Stay away from this product See Less
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Noticed our dog started acting constipated and neurogically strange after eating these a couple of months, then it came to a head. We thought we were going to lose her, took her off these peanut butter treats and now her seizures and constipation have digressed. | Symptoms: Other See Less
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I have been giving my dogs dream bones since I found them. They love them and I love that they were rawhide free. I had no idea that the issue with my little dogs could be caused by them until reading similar stories. I have 3 chihuahuas.... See More The first thing was when I noticed my oldest dog's bleeding rectum. It almost poured out. The vet said to watch him because it could be a ruptured anal gland. I found it odd to be that when the blood had zero signs of stool in it. His hemorrhaging stopped that evening and he did better with no follow up. The middle dog who is my companion dog I woke up to being extremely sick. Lethargic and just cried when getting close to her. She couldn't get off my pillow. I rushed her to the emergency vet and have never been treated so horrible by anyone. My fear for her and being without her was extreme. He didn't like that at all. I left and asked they call me as soon as anything was found out. When I called that late afternoon I realized that they closed overnight. I panicked at the thought of her being there alone, scared, and sick all night. The Dr never would call me back. I showed up 5 min to close to find him sitting doing nothing. I took a picture yet the vet told me he was too busy to call. He was irate with me for showing up unannounced. He said she was extremely sick and would not likely make it. When I asked what was wrong he said he didn't know I showed up take her elsewhere. I was already at the emergency vet? He walked out of the room and never told me what was wrong or done. They said she had extreme white blood count and dehydration. They gave her a shot of antibiotics and fluid and chargedmeover $600. The next morning I called her regular vet and have had to take her back every 2 weeks for 2 months. They don't know what is going on. I am on disability and with very limited funds. I am not loosing my house of 11 years because of money spent. Never having enough to have her uthinized or surgery. Repeat visits have been my only option. Care credit says I don't have enough or reliable income for a loan over services. I have been on disability for 14 years. I am now calling my vet to ask about dream bone issues with other pets. I feel like these have almost killed 1 dog and slowly killing another. I wish they would make this information public where they still sell them and continued to the whole time there has been concern. 😭😭

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A tree falling through a transmission line on Whitlock Road caused a widespread power outage Wednesday afternoon in Henry County.
Shortly before 4 p.m., more than 4,000 people across Henry County lost power because of the fallen line, according to Paris Utility Authority.
About 4:30 p.m., PUA... See More was able to restore power everywhere except Puryear, according to a spokesman. About 1,700 Puryear residents were still said to be without power.

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As of 8:30 a.m., several thousand people are waking up without power after the first line of storms move through.

DAVIDSON COUNTY: 970
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As of 8:30 a.m., several thousand people are waking up without power after the first line of storms move through.

DAVIDSON COUNTY: 970
CHEATHAM COUNTY: 115
MONTGOMERY COUNTY: 480
ROBERTSON COUNTY: 102
STEWART COUNTY: 274
SUMNER COUNTY: 7
DICKSON COUNTY: 864

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DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.

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American Screening LLC of Shreveport, Louisiana is voluntarily recalling 153,336 units of Hand Sanitizer, containing 70% ethyl alcohol gel to the consumer level. The hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption.

Risk Statement: Ingesting hand sanitizer, which... See More 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, American Screening LLC 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 an eight-ounce bottle. The affected hand sanitizer lots include the following expiration dates of 5/21/2022 and 05/24/2022 for black-capped bottles and no lot numbers or expiration dates for clear capped bottles. The product can be identified by its shape (small water bottle), with a black flip top cap or clear cap with blue pouring spout with the weight of measure of eight (8) ounces/237mL, UPC 8 4005051579 2.

The Hand Sanitizer was sold to customers & distributors Nationwide via the internet at americanscreeningcorp.com and/or in-house sales.

Consumers & distributors that have this hand sanitizer which is being recalled should stop distribution/use and return to place of purchase or discard. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to ingesting the hand sanitizer packaged in the 8 oz. water bottle style.

Company name: American Screening LLC
Brand name: American Screening
Product recalled: Hand Sanitizer
Reason of the recall: Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption
FDA Recall date: November 19, 2021

Check the full recall details on fda.gov

Source: FDA
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Nutrisure Ltd is recalling Naturya Hemp Protein Powder because it contains gluten, which is not mentioned on the label. This means the product is a possible health risk for anyone with an allergy or intolerance to gluten. This batch was only sold in Sainsbury’s stores.

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Pack size: 100g
Batch code: W02135
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If you have bought the above product and have an allergy or intolerance to gluten, do not eat it. Instead, return it to the store from where it was bought for a full refund.

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Brand: Boba Origin. Product: 100% Whey Protein Isolate. Flavor: Brown Sugar Milk, Tea, Undeclared milk, & soy. Size: 1 gallon plastic jar. Lot No. 2106263. Exp. 07/2023

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Brand: RAW. Product: Vegan Protein Flavor: Peanut Butter, Undeclared coconut. Size: 1gallon plastic jar. Lot No. 2108070, 2104340, 2102018, 2012304, 2010266, 2010102, 2007037/746, 2005132. Exp. 08/2023, 04/2023, 02/2023, 12/2022, 10/2022, 10/2022, 07/2022, 05/2022

Brand: Steel. Product: Veg-Pro Flavor: Cookies & Crème, Undeclared Wheat. Size: 64 ounce plastic jar. Lot No. 2109390, 2104333, 2011260, 2104007/1041, 2105059, 2011260/994. Exp. 09/2023, 04/2023, 11/2022, 04/2023, 05/2023, 11/2022

Brand: Vital Force. Product: PureISO. Flavor: Milk Chocolate, Cocoa, Undeclared milk. Size: 1gallon plastic jar. Lot. No. 2108191. Exp. 09/2023

Brand: Vital Force. Product: PureISO. Flavor: Creamy Peanut, Butter Vanilla, Undeclared milk. Size: 1gallon plastic jar. Lot No. 2109068. Exp. 09/2023

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall.

This recall is being made with the knowledge of the Food and Drug Administration.

Company name: Nutracap Holdings, LLC
Brand name: Etedream, Vital Force, Raw, Boba Origin, Steel
Product recalled: Dietary Supplement Protein Powder
Reason of the recall: Undeclared wheat, milk, soy and/or coconut
FDA Recall date: November 09, 2021

Check the full recall details on fda.gov

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Livia Global, Inc announced the recall of two lots of its liquid probiotics, LiviaOne Liquid Probiotics & BioLifePet Liquid Probiotics, due to the possibility of contamination by Pseudomonas aeruginosa, a microorganism that can cause life-threatening infection in immunocompromised individuals. These products are distributed nationwide through Amazon, wholesale,... See More and direct sales from the company’s website.

Pseudomonas aeruginosa is a microorganism found in the environment that, if ingested, can cause life-threatening infection in immunocompromised individuals. P. aeruginosa infections are generally limited to hospital settings.

This recall only affects the following products with the Lot# 001005-1 Best by: 04/2023 & LiviaOne Nasal Probiotics with Lot# 010620-1 Best by 08/2023 with the following ship dates:
- LiviaOne Daily Probiotics 2oz – UPC 030915 107112 Ship dates 04/16/2021 – 08/30/2021 (1067 units)
- LiviaOne Daily Probiotics 4oz – UPC 030915 107167 Ship dates - 07/09/2021 – 08/30/2021 (384 units)
- LiviaOne Topical Spray Probiotics 4oz – UPC 030915 107105 Ship dates 07/08/2021 – 07/30/2021 (571 units)
- LiviaOne Nasal Probiotics 1oz – UPC 030915 107198 Ship dates 04/21/2021 – 05/12/2021 (480 units)
- LiviaOne Nasal Probiotics 1 oz - UPC 030915 107198 Ship dates 07/14/2021 – 08/24/2021 (600 units)
- LiviaOne Nasal Probiotics 1 oz – Lot# 010620-1 UPC 030915 107198 Ship dates 10/27/2021 – 11/25/2021 (50 units)
- BioLifePet Probiotics for Cats – UPC 030915 107044 Ship dates 05/05/2021 – 07/26/2021 (128 units)
- BioLifePet Probiotics for Dogs – UPC 030915 107037 Ship dates 05/05/2021 – 08/25/2021 (128 units)

Lot numbers are located on the side of the bottle and on the bottom of the outer container in which the product is sold. No other lots or ship dates or any other LiviaOne products are affected by this recall.

Company name: Liva Global, Inc.
Brand name: LivaOne and BioLifePet
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Reason of the recall: Pseudomonas aeruginosa
FDA Recall date: December 01, 2021

Check the full recall details on fda.gov

Source: FDA
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Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products.

Risk Statement: Benzene is... See More classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.

To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See the link below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically the ones listed in the link below.

The products were distributed nationwide in the United States through various retailers. Consumers, distributors, and retailers that have product which is being recalled should stop using or selling these specific Odor-Eaters® spray products and dispose of them appropriately.

Company name: Odor-Eaters®, owned by Blistex Inc.
Brand name: Odor-Eaters®
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FDA Recall date: November 17, 2021

Check the full recall details on fda.gov

Source: FDA
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Mountain Meadow Herbs of Somers, MT is recalling 54 bottles (total 240 capsules per bottle) of Mountain Meadow Herbs brand Candida Flush, Lot# 0120011Q. Some bottles from this Lot have become pressurized over time in storage. When opened, the product may forcefully expel air as well as... See More portions of capsules and powder. This may result in customers sustaining injuries to their hands and eyes, which may require medical attention.

Product was distributed to retailers in IN, MN, MT, NY, TN and in Ontario of Canada.
Product was sold directly to consumers in IN, KY, MN, MO, MT, NE, OH, PA, VA, and WI. The affected Candida Flush has the UPC 8 13086 01593 2, Lot #012001l Q, Exp 12/22.

No illnesses or serious injuries have been reported to date. The recall was the result of an internal investigation stemming from a customer complaint which revealed that the finished products were becoming pressurized over time.

This recall is being made with the knowledge of the U.S. Food and Drug Administration. If you have any of these products, please dispose of them immediately.

Company name: Mountain Meadow Herbs
Brand name: Mountain Meadow Herbs
Product recalled: Candida Flush
Reason of the recall: Due to exploding bottle risk
FDA Recall date: November 17, 2021

Check the full recall details on fda.gov

Source: FDA
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Sagent Pharmaceuticals, Inc. on November 19 announced the voluntary nationwide recall of four lots of Levetiracetam Injection, USP, to the user level. The lack of container closure integrity, found in reserve sample vials may result in a non-sterile product.

Risk Statement: Intravenous administration of a product intended... See More to be sterile that is not sterile could result in serious systemic infections which may be life-threatening. 

To date, Sagent has not received reports of any product complaints or adverse events associated with this issue. Levetiracetam Injection, USP 500 mg per 5 mL, is used in the treatment of certain types of seizures and is packaged in a 5mL single-does vial. The Levetiracetam Injection, USP, label and affected lot numbers with Expiration Dates and NDC number can be found in the table below. 

Product: Levetiracetam Injection, USP / Lot Number: B0G85VB /Expiration Date: Jun-2022 / NDC Number: 25021-780-05 / Distribution Dates: May 2021 - August 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K88VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: March 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K89VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: August 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B1G194A /Expiration Date: Jun-2023 / NDC Number: 25021-780-05 / Distribution Dates: October 2021.

The product was distributed Nationwide from March to November  2021.

Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Levetiracetam Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: November 22, 2021

Check the full recall details on fda.gov

Source: FDA
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