Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case!
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Add Photo/Video
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!


IMPORTANT - Your report is queued
It may take up to 12 hours to process your report.


Email us at support@safelyhq.com if you have questions.

Report by
Loading...
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Mid America Pet Food Dog and Cat Food update- recalled due to Salmonella contamination, USA

3 weeks ago

United States

Mid America Pet Food, Mount Pleasant, Texas, is expanding its October 30, 2023, voluntary recall to include additional pet food products, with Best By Dates before 10/31/24, made at its Mount Pleasant facility, due to the products’ potential to be contaminated with Salmonella. These products were distributed to distributors and retailers throughout the United States. As of November 1, 2023, seven people reported Salmonella infections.

Voluntarily recalled brands produced at the Mount Pleasant facility include: Victor Super Premium Dog Foods, Wayne Feeds Dog Food, Eagle Mountain Pet Food, and some Member’s Mark varieties with Best By Dates before 10/31/24. The affected products are shown in the images below.

The Best By Date is found on the middle top of the back of each bag. This expanded voluntary recall is being issued due to some of the product lots testing positive for Salmonella through random and targeted sampling of finished product, including by the firm and the South Carolina Department of Agriculture.

Salmonella can affect animals eating the products, and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have may only exhibit decreased appetite, fever, and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

Retailers and distributors should immediately pull all product from their inventory and shelves and destroy product. Do not sell or donate the recalled products. Do not feed the recalled product to pets or any other animals. Destroy the food in a way that children, pets, and wildlife cannot access. Wash and sanitize pet food bowls, cups, and storage containers. Always ensure that you wash and sanitize your hands after handling recalled food or any utensils that come in contact with recalled food.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Mid America Pet Food
Brand name: Multiple brand names
Product recalled: Dog and Cat Food
Reason of the recall: Potential to be contaminated with Salmonella.
FDA Recall date: November 09, 2023

Source: fda.gov

292


Related Reports

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
269


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
290


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
290


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
23


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
290


Ordered 3 space heaters ... they were delivered in crushed old boxes and don't work calling credit card company for refund See Less


The Boil Water advisory issued for customers in the city of Glendale, Oregon has been lifted, according to the City Manager.

Source: kezi.com
Published: 2023-12-06 See Less


A boil water order has been issued for customers in Weirton following work on a water line along Cove Road. The order is in effect for the 400 block of Cove Road, as well as Overbrook Drive, Garden Way and Spring Street, as well as any other... See More water customers in the area who lost pressure.

Source: weirtondailytimes.com
Published: 2023-12-06
See Less


A power outage has been reported in Riverdale today December 6th at 11:25 a.m. Customers affected: 147. Cause of the outage: Patrolling.The estimated restoration time is today, December 6 at 5:45 p.m.

Outage link: pgealerts.alerts.pge.com
Source: lostcoastoutpost.com
Published: 2023-12-06 See Less


An electrical service disruption was reported in sections of Deep Gap on Wednesday morning. According to Blue Ridge Energy's outage map, hundreds of customers were without power due to high winds. Those outages began at 11:55 am and ended at 1:59 pm. The most affected areas were:... See More Caldwell county with 251 customers affected, Watauga County 413 with customers affected. Power has been restored to the area.

Outage link: bremco.maps.sienatech.com
Source: wataugaonline.com
Published: 2023-12-06
See Less


Recent Interesting Reports

I thought I ordered from QVC and I have snow shovel ordered 11/15/23 email sent that it shipped 11/17 with a tracking number when I try to track it shows # not f**** what are my options See Less


I ordered some makeup on Facebook .and I reached out to the company because I hadn't received my order.they told me they don't send orders outside of Brazil.I don't want this Mark Cadicamo to charge me again or send me anything else. See Less


I receive a red band watch that I didn’t order. I don’t know how they got my information!!
From 371 Little Falls Road- Unit 4, Cedar Grove NJ 07009. Can you please let me know how they got my information! Thank you! See Less
645


Teapa you don't order are ordinary See Less
21


BE
b...........u
ATENTIE TEAPA MAGAZIN DIN CHINA !
Sunati firma curierat apoi mergeți la poliție!
Reply 19 hours ago

Like many others, I'd ordered from a Bed, Bath & Beyond site and was scammed, then received a pkg with charging cables. I'm in Illinois. Pkg was sent from
Family Medical LLC (fake name obviously)
11-15 124th ST
College PT, NY 11356. See Less
2.7K


Last 30 days