Dogs Choice UK frozen raw dog foods - recalled due to the presence of Salmonella, England, UK

1 year ago

England, United Kingdom

Dogs Choice UK is recalling a number of frozen raw dog foods because Salmonella has been found in the products.

- Frozen Chicken and Beef (500g). Batch code: 080222+2. Best before: 08 August 2022
- Frozen Chicken and Beef Ready Meal (500g). Batch code: 080222+2. Best before: 08 August 2022
- Frozen Chicken Liver (500g). Batch code: 080222+2. Best before: 08 August 2022

If you have bought any of the above products do not use them. Instead, return them to the store from where they were bought for a full refund. When handling and serving raw pet food it is always advised to clean utensils and feeding bowls thoroughly after use. Consumers should wash hands thoroughly after handling raw pet food, bowls, utensils or after contact with the faeces of animals.

Raw pet food should be stored separately from any food (especially ready to eat foods). Care should be taken when defrosting to avoid cross contamination of foods and surfaces.

The presence of Salmonella in the products listed above. Salmonella is a bacterium that can cause illness in humans and animals. The product could therefore carry a potential risk, because of the presence of Salmonella, either through direct handling of the pet food, or indirectly, for example from pet feeding bowls, utensils or contact with the faeces of animals.

In humans, symptoms caused by Salmonella usually include fever, diarrhoea, and abdominal cramps. Infected animals may not necessarily display signs of illness, but symptoms can include diarrhoea.

Company name: Dogs Choice UK
Product recalled: Frozen Chicken and Beef, Frozen Chicken and Beef Ready Meal, Frozen Chicken Liver
FSA Recall date: 02/17/2022

Check the full recall details on food.gov.uk

Source: FSA

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I bought the dream bone twist today at family Dollar... I gave my puppy one and she ate it... About 3-4 hrs later she was vomiting and got very weak and couldn't walk... Hours later she is still vomiting and very sick... | Symptoms: Vomiting, Weakness, Fatigue See Less

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Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the Novum IQ syringe infusion pump. The Correction is due to the potential for an incomplete infusion following one or more downstream occlusion alarms. Baxter notified impacted customers in October and is developing... See More a software upgrade to resolve the issue. There have been no reports of serious injury associated with this issue to date. This infusion pump was distributed in the United States.

Baxter has identified that after one or more downstream occlusion alarms occur on the Novum IQ syringe pump, the pump may display an “Infusion Complete” alarm despite fluid remaining in the syringe. This could lead to an underdose and/or interruption of therapy. The difference between the remaining volume to be infused displayed on the pump and the volume left in the syringe is dependent on the number of occlusion alarms encountered during an infusion and the size of the syringe being used.

If a patient does not receive the intended dose of a prescribed medication, serious or critical adverse health consequences may occur. Potential health consequences are dependent on multiple patient-specific factors (such as disease state as well as age and weight of the patient involved, and the care area where they are treated), occlusion pressure settings, the number of occlusions that occurred, the size of the syringe used, and the therapy being delivered.

This Urgent Medical Device Correction applies to Novum IQ syringe infusion pump with product code 40800BAXUS. Baxter has contacted affected customers and is developing a software update to resolve the issue. Until the software update is available, customers can continue to use Novum IQ syringe infusion pumps with the following reinforced guidance provided by Baxter:

- As stated in the pump’s Operator’s Manual, users should choose the smallest compatible syringe size necessary to deliver the fluid or medication.
- Prior to beginning an infusion, users should ensure the downstream occlusion pressure setting is appropriate for the clinical scenario. Consistent with standard clinical practice, users should always check for clamped lines and other sources of downstream occlusion prior to and during therapy. Pressure setting selection guidelines and instructions for downstream occlusion resolution can be found in section 8.8 of the Operator’s Manual.
- Per standard clinical practice, users should continue to monitor the “Volume to be Infused” and the volume delivered while therapy is in progress. This is especially true after a downstream occlusion alarm has occurred. Users should also take note of the initial volume and compare it to the final volume in the syringe. If the total dose is not delivered upon the “Infusion Complete” alarm, users should reprogram the pump and deliver the remaining volume as necessary.

In case you experience harm from this product, 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.

Company name: Baxter International, Inc.
Brand name: Baxter
Product recalled: Novum IQ syringe infusion pump.
Reason of the recall: Potential for an incomplete infusion following one or more downstream occlusion alarms.
FDA Recall date: November 30, 2023

Source: fda.gov See Less

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Meta Herbal is voluntarily recalling 500 blister packs of Magnum XXL 9800 2000 mg per capsule, to the consumer level. The products have been found to be tainted with Sildenafil. Products containing sildenafil cannot be marketed as dietary supplements. Magnum XXL 9800 capsules is an unapproved new... See More drug for which safety and efficacy have not been established and, therefore, subject to recall. The product was distributed and sold online on Amazon under the ASINs: B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ. To date, Meta Herbal has not received any reports of adverse events related to this recall.

Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) found in FDA-approved products for the treatment of male erectile dysfunction.

Risk Statement: Consumption of products with undeclared sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life-threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.

The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in blister packs of one pill, with a UPC 645759993007 exp 1/2025. Each blister pack is sold individually and holds one capsule.

Meta Herbal is notifying its customers via Amazon and is arranging for refunds. All blister packs of Magnum XXL 9800 are affected by this recall. Consumers who have the recalled product should stop using it and contact Meta Herbal for return/refund instructions.

In case you experience harm from this product, 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.

Company name: Meta Herbal
Brand name: Magnum
Product recalled: Magnum Male Sexual Enhancement XXL 9800 capsule
Reason of the recall: Undeclared Sildenafil
FDA Recall date: November 29, 2023

Source: fda.gov See Less

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After eating a Dreambone Peanut Butter Pretzel Stick this morning, my dog vomited +6 times and had runny diarrhea all throughout the day. Several times during the diarrhea he couldn't get anything out and yelped in pain. I first bought these treats a couple weeks ago and... See More he had the same symptoms afterward the first time. I didn't realize it was the Dreambone treats until I gave him a second one today. I will do everything in my power to spread the word that Dreambone's treats are horrible, causing painful diarrhea, vomiting, and death. Why haven't these been recalled and/or banned after multiple proven lawsuits and cases against them? | Symptoms: Diarrhea, Vomiting See Less

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Novartis is conducting a voluntary nationwide recall at the consumer level of two lots of its Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL in the US due to crystal formation observed in some bottles, which could potentially result in incorrect dosing. The issue was identified... See More during an investigation of crystallization in a different lot of Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL. No other Sandimmune formulations are impacted. They were distributed nationwide to wholesalers across the US, beginning in January 2022 and September 2022, respectively. Novartis has not received any reports of adverse events related to this recall, to date.

Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL, packaged in 50 mL bottles, is indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. The drug may also be used in the treatment of chronic rejection in patients previously treated with other immunosuppressive agents.

Risk Statement: Crystallization of cyclosporine in Sandimmune Oral Solution is likely to result in non-uniform distribution of the cyclosporine in the product, resulting in under-dosing or over-dosing. There is a reasonable probability that under-dosing may result in lower exposures and decrease in efficacy which could ultimately lead to graft rejection and graft loss in transplant patients. Furthermore, over-dosage may manifest itself as cyclosporine toxicity in the long term if overexposure continues.

The affected lot numbers and expiration dates are:
- FX001500 (expiration date 09/2024)
- FX001582 (expiration date 09/2024) NDC 0078-0110-22.
These lots were only distributed in the US.

Novartis is notifying its distributors via a recall notification letter and is arranging for the return of the recalled lot from distributors, retailers, and consumers. Additionally, Novartis is notifying healthcare providers who have prescribed this product to contact their patients. Consumers who have bottles from the recalled lot of Sandimmune Oral Solution (cyclosporine oral solution, USP), 100mg/mL, should contact their healthcare provider.

In the event that a patient experiences an adverse reaction or quality problem involving this product, they should immediately contact their healthcare provider.

In case you experience harm from this product, 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.

Company name: Novartis Pharmaceuticals Corporation
Brand name: Novartis
Product recalled: Sandimmune (cyclosporine oral solution, USP) Oral Solution 100 mg/mL
Reason for the recall: Due to crystallization formation
FDA Recall date: November 27, 2023

Source: fda.gov See Less

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I had placed an order on 06/10/23 but I haven’t received anything- missing order. Awaiting an update, please. The seller is “great sale. Com. And I spent 72.28US $. What should I do now? I tried to contact them but couldn’t get through. But hopeless. See Less

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You charged my credit card for $36.49 on 11-13.  I still have not gotten any info or delivery?   What is up? See Less

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I've bought something and never received it. The email is not valid.
I've also got bit by norskla. ComAllworldcruise. Com. and lastly naisiton See Less

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I have bought shoes , I did not received it until 15 days exactly after I called my bank to stop the payment. Unfortunately the payment gone then they sent it . I have returned this shoes as it is a rubbish shoes . I did not... See More get my money until today. Unit 15 Tay Road, Frankley Industrial Park Birmingham. I have connected with this scammer through facebook. I wish to help me to return my money back See Less

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I recieved a parcel I did not order See Less

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I ordered two pair of shoes that were advertised to be most comfortable shoes for your feet while walking. Also best for nureopathy. They are terrible and cheap. Looks like they are made of cardboard and its like walking on a concrete floor. Not what was advertised... See More at all. I am disputing the charge with my credit card company. they advertised on Facebook. See Less

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I received a package I didn’t order. It says it is smart fairy lights. I have never ordered anything from this company nor have I even heard of them. See Less

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An empty cell phone projector box. Wrapped in dark grey plastic and taped closed. Had two labels; a US shipping label (which has the word ‘Advantage’ misspelled as ‘Advatage’) and another one from overseas underneath of it. I never ordered anything. Yes. An empty cell phone projector... See More box. Sent from ‘Jane’ 371 Little Falls Rd Suite 4 Cedar Grove, NJ 07009 I peeled off the secondary shipping label and found: the letters JIT in parentheses, originally sent from: Maybe Japan? China? I’d send a pic of the label if I could. What appears to be a tracking sequence: LBX02219513996****** See Less

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The order was expected to be delivered within 12 to 20 days. What happened was that when it completed 20 days, it appears as delivered on the carrier's website. However, the website of the company that made the purchase does not contain the order or the items... See More I purchased anymore. I send an e-mail and no one answers me. In the e-mail from the company that charged my card they replied saying that the order had been delivered. However, I saw on the carrier's website that many people have the same problem of undelivered orders. See Less

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KinderFarms, LLC is voluntarily recalling all lots of KinderMed Infants’ Pain & Fever (oral suspension) and KinderMed Kids’ Pain & Fever (oral suspension) to the retail and consumer level. These products are being voluntarily recalled due to acetaminophen instability. These products are available nationwide in drug/pharmacy, supermarkets,... See More direct delivery and national retailers, and online through major ecommerce sites. The company has not received any reports of serious adverse events from either of these products to date.

The two products were manufactured and packaged for KinderFarms by a major, U.S.-based OTC pharmaceutical manufacturer with over 30 years of experience. Ongoing testing of sample batches indicated some product lots were no longer in specification and may pose a health risk. Acetaminophen is the active ingredient in many pain-relieving medicines. As a result of the potential health risk with acetaminophen being outside of specification, the product may cause acute adverse health effects, including abdominal pain, nausea, vomiting or jaundice at higher doses.

This voluntary recall encompasses all products currently available on shelf of these two SKUs only. The impacted product being voluntarily recalled is all lots of:
- KinderMed Infants’ Pain & Fever (2 fluid ounces/59 mL), (Acetaminophen - 160 mg per 5 mL), Oral Suspension. UPC: 850001805698
- KinderMed Kids’ Pain & Fever (4 fluid ounces/118 mL), (Acetaminophen - 160 mg per 5 mL), Oral Suspension. UPC: 850001805728

Consumers who purchased either of these two products should stop using them and may return the product to the place of purchase for a full refund.

In case you experience harm from this product, 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.

Company name: KinderFarms, LLC
Brand name: KinderMed
Product recalled: OTC Pain and Fever Reliever for Infants and Kids
Reason of the recall: Due to Acetaminophen Instability
FDA Recall date: November 17, 2023

Source: fda.gov See Less

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I did order the dress I received but it is not the quality or description of what I ordered. There’s no way to return for a refund since the address on the label is a residential home that is not this company. No company name , the... See More USPS tracking number has no information when searched either! Just a waste of money I assume! The address on the shipping label is 609 cattle chut ct in celina Tx but underneath has a Chinese looking label. I’m not sure what’s going on but I can’t find any information on the “company” at all! See Less

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Contents: Gray box w/bow; fake adjustable diamond ring. "GRA" limited warranty card; GRA Moissanite Report
I am in Hamilton, OH See Less

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Received 2 packages same day. Similar type labels different sender addresses. One package had my address but different name. Second pkg addressed to me with correct address. My package contents were 6 cheap necklaces individually wrapped. I opened second package before I realized it was not addressed... See More to me. It contained two pins with a sport logo. Googled both sender addresses and they both appeared on this site as scammers. Appears to possibly be related to online purchases which are fulfilled with cheap junk totally unrelated to items ordered. No way to obtain refund or contact vendor. See Less

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Ordered a Stanley tumbler on 11/25/23. S opposed lt shipped 11/28/23-tracking received doesn’t work. Pretty sure I’ve be scammed. Advertised on IG. See Less

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I received a package from here it’s hair growth oil that I didn’t order, and it’s also broken the box inside the plastic is wet.
SPF2311113**** See Less

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