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Dunkin', 876 Edgell Rd, Framingham, MA 01701, USA
Latest report: May 28, 2020 12:00 PM
CF
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.
Source: framinghamsource.com See Less
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35
Detect, Inc. Over the counter Covid-19 Test - recalled due to may give false negative results, USA
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,... See More 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
Source: fda.gov See Less
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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... See More 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.
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Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination, USA
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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... See More 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
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