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: email@example.com
Goodbye! and best wishes in your recovery
Dunkin' Employee Test Positive For COVID -19
3 years ago
An employee at the Dunkin’ on Edgell Road has tested positive for COVID-19. the employee last worked on May 25. If you visited the restaurant during that time, please report it and any other location that you visited.
Papa johns is not protecting their employees from COVID, Papa Johns Pizza, 9123 N Loop 1604 W, San Antonio, TX 78249, United States
3 months ago
Papa johns is not protecting their employees from COVID. I just got COVID and strep tested and it came back positive for both. They immediately told me to come back to work. This is completely unsanitary and unsafe for employees and customers. They are not following protocols... due COVID -19 and are disregarding everything just to have the correct amount of staffing.
I started feeling symptoms yesterday morning after eating at this location in Dunn. The location was very dirty and none of the people wore masks. I have had to cancel my driver's test, dentist appointment, doctor's appointment and several other events. | Symptoms: Other
I was staying at a shelter in Lockport Cares and there was a Christian pastor at the shelter. Guess again. I dialed an ubulanxe to go to the hospital because my teeth were bleeding.and I was coughing up blood. The woman told me I should not stay... at Lockport Cares because I called an ambulance to go to the hospital.
I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.
For 2 nights there is always corn or brownies during Bible study at 8pm at night.
I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.
My blood sugar was low and I was coughing up blood and my teeth were bleeding.
Warning. Lockport Cares does food poisoning
Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
You are not required to wear mask indoors.amd of you are positive for covid 19, you are not required to wear a mask. There is a woman positive for covid 10 not wearing a mask everyday spreading her disease. Lockport Cares allows kids and married couples to stay the night also.
Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.
Warning. | Symptoms: Cough
11 months ago
Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, their molecular, over-the-counter test used to identify SARS-CoV-2 (the virus that causes Covid-19) in self-collected nasal swabs. The recall affects a total of 11,102 tests shipped to customers from July 26th, 2022 through August 26th,... 2022. The test was granted Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) on October 28, 2021. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution.
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. The reliability of positive test results is not affected.
Below is a list of the affected lots. The lot number can be found on the side of each test box along with the Use By date.
Lot Number: HB264, Use By Date: 1/1/2023, Number of Tests Shipped: 7,382
Lot Number: HY263, Use By Date: 1/1/2023, Number of Tests Shipped: 1,800
Lot Number: HY264, Use By Date: 1/1/2023, Number of Tests Shipped: 1,920
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution. The reliability of positive test results is not affected.
Detect is notifying all customers and distributors affected by the recall. Anyone in possession of any unused tests from the affected lots should dispose of the tests. The outer packaging is recyclable while all the test components can be discarded as regular trash. Detect Hubs are not affected by the recall and do not need to be discarded.
Test users who attempt to use recalled tests will be notified in the Detect App™ that the test has been recalled and may not be used.
Detect, Inc. will issue a refund* for the affected tests (as verified by Detect) upon customers’ acknowledgement of receipt of the recall-related communication and confirmation that any affected tests in possession have been disposed of.
Company name: Detect, Inc.
Brand name: Detect
Product recalled: Over the counter Covid-19 Test
Reason of the recall: There is an increased chance that the tests from the lot numbers listed below may give false negative results
FDA Recall date: December 12, 2022
11 months ago
We presumed we had bad food but it turned out to be the latest covid variant. Extreme stomach pain and headache, along with bad bowel and bitter mouth. Not like the extreme fatigue and sinus of the last few rounds of SARS-Co-V-2. There was an issue with... chorizo fat in a breakfast burrito that added to it, however that was not the main culprit, just difficult to digest (apparently for many). A tasty evil. Currently in California | Symptoms: Headache, Fatigue, Stomach Pain
4 months ago
As winds and rain swept through Massachusetts, the city of Framingham was particularly hard hit. A storm blasted through the city at about 2:45 p.m. with blinding downpours, frequent lightning and strong winds, taking down dozens of trees and leaving several neighborhoods without power and closing roads....
Outage link: outagemap.eversource.com
More than 575 customers in Framingham are without power this morning, mostly in the north section of the City. The power outage is mostly in the Nobscot section, along Edgell Road and Edmands Road. Eversource is reporting about 2% of the City’s customers are without power. It... is unknown at this time why the outage happened. Eversource is reporting power should be restored by 9 a.m.
Outage link: outagemap.eversource.com
About 2,100 residents in North Framingham, mainly in the Saxonville neighborhood, are without power. Eversource did not note the cause of the outage, but power is also out in parts of the Town of Wayland too.
Outage link: outagemap.eversource.com
Recent Interesting Reports
I got in Mail today and didn't order. Slim detox keto advanced 800 mg and gummies., Wichita Falls, Texas, USA
3 weeks ago
I got in Mail today and didn't order. Slim detox keto advanced and gummies. Again I didn't order. Hope nothing is being charged to me. I am don't really know what it's for. I am definitely not over weight or anything.
2 weeks ago
I keep receiving a package from this address with 2 bottles of male enhancement and testosterone booster which I never order. I cannot stop from coming. There is no phone or anything in package
1 week ago
I received a pkg from Seller 2800 N Franklin Road Indianapolis IN 46219 that I did not order. There was no receipt or company name. It was a moissanite heart necklace with a GRA Moissanite Report. What kind of scam is this?
No energy in the Weiser block
CDC, public health and regulatory officials in several states, and the U.S. Food and Drug Administration Center for Veterinary Medicine (FDA CVM) are investigating a Salmonella Kiambu multistate outbreak linked to Dry Dog Food. As of November 1, 2023, 7 people infected with the outbreak strain of... Salmonella have been reported from seven states (AL, CA, FL, HI, KY, MN, and OK). One person was hospitalized and no deaths have been reported. Illnesses started on dates ranging from January 14, 2023, to August 19, 2023.
People in this outbreak got sick from touching recalled dog food, touching things like dog bowls that contained the dog food, or touching the poop or saliva of dogs that were fed the dog food. Most of the sick people in this outbreak are infants. Epidemiologic and laboratory data show that a specific lot of Victor brand Hi-Pro Plus dry dog food is contaminated with Salmonella and has made people sick. The manufacturer, Mid America Pet Food, has recalled this and all other brands of pet food they make. Investigators are working to identify any additional products that might be contaminated.
On September 3, one lot of Victor brand Hi-Pro Plus dog food was recalled. Affected products: 5-pound bags with lot code 1000016385. Best-by date 4/30/2024.
On October 30, three lots of Victor Super Premium Dog Food, Select Beef Meal & Brown Rice Formula were recalled. Affected products: 5 pound, 15 pound, and 40 pound bags Best-by date 6/12/2024 Lot numbers 1000016890, 1000016891, 1000016892.
On November 9, Mid America Pet Food recalled all brands of pet food they make. Affected products: All dog and cat food, Best by dates before 10/31/2024, Brands include: Victor Super Premium Dog Foods, Wayne Feeds Dog Food, Eagle Mountain Pet food, Member’s Mark. Multiple bag sizes including: 5 pound, 15 pound, 16 pound, 30 pound, 40 pound, and 50 pound.
The CDC advises the following to Pet Owners:
- Throw away recalled pet food in a sealed trash bag and place it in a sealed trash can so that wildlife cannot get to it. Don’t let children touch the recalled pet food. Don’t feed recalled pet food to pets or other animals. Don’t donate recalled pet food.
- Clean surfaces and items, including pet items like bowls, that might have touched the recalled pet food.
- Contact a veterinary care provider if your pet has any of these symptoms after eating the recalled pet food: Vomiting, Diarrhea (may be bloody), Fever, Loss of appetite, Decreased activity level
- Contact a healthcare provider if you or your child have any of these severe Salmonella symptoms: Diarrhea and a fever higher than 102°F, Diarrhea for more than 3 days that is not improving, Bloody diarrhea, So much vomiting that you or your child cannot keep liquids down, Signs of dehydration, such as: Not peeing much, Dry mouth and throat, Feeling dizzy when standing up.
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.
1 week ago
Bayer is voluntarily recalling one lot of Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles to the consumer/user level. The product is being recalled due to microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing. It was distributed to wholesale distributors and... specialty pharmacies nationwide between January 3, 2023, and February 13, 2023. To date, Bayer has not received any adverse events related to this recall.
Risk Statement: Vitrakvi® is indicated for the treatment of solid tumors that are NTRK gene fusion positive, it is expected that patients on Vitrakvi® may be immunocompromised. Although there is little data in the literature on human pathology caused by Penicillium brevicompactum, there are cases of invasive disease caused by similar Penicillium species, particularly in patients with underlying immunosuppression. Therefore, there is a reasonable probability that ingestion of Penicillium brevicompactum in patients on Vitrakvi® with underlying immunosuppression may result in invasive fungal infections of the blood or pneumonia that can be life-threatening.
The impacted lot of Vitrakvi® is packaged in a 100mL glass bottle with NDC# 50419-392-01 and is identified with Lot# 2114228 and an expiration date of February 29, 2024. Product bottle and carton label images and information on the lot number that falls under this recall is attached
Bayer notified all distributors and pharmacies of this recall on November 8, 2023. Bayer has engaged Qualanex to manage the recall of the product down to the consumer level. Qualanex has notified Vitrakvi® distributors via a recall notification letter and will arrange for the return of the recalled lot from distributors, specialty pharmacies, and consumers.
Consumers who have the recalled Vitrakvi® product should immediately stop use of this particular lot of product and contact their physician or healthcare provider if they have any questions, concerns or have experienced any problems related to Vitrakvi® Oral Solution 20 mg/mL.
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: Bayer
Brand name: Bayer
Product recalled: Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles
Reason of the recall: Microbial contamination identified as Penicillium brevicompactum
FDA Recall date: November 21, 2023
Last 30 days