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416 Diner, 416 E 5th St, Dayton, OH 45402, USA

Latest report: July 6, 2020 12:00 PM
#coronaviruscovid19 #416east5thstreet #dayton #ohio #unitedstates
PP

Employee test positive for Covid-19

2 years ago

Ans employee at 416 Diner in Dayton’s Oregon District tested positive for COVID-19. The employee has not worked at the diner since June 27.

Source: dayton.com See Less
709


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Recent Interesting Reports

Edgewell Personal Care Company (NYSE: EPC) today issued a voluntary nationwide recall of three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 to the consumer level as outlined in the list below. An internal review found that some samples of the product contained trace... See More levels of benzene. While benzene is not an ingredient in any Banana Boat products, the review showed that unexpected levels of benzene came from the propellant that sprays the product out of the can. To date, Edgewell has not received any adverse events related to this recall. The products were distributed nationwide in the United States through various retailers and online. Edgewell has notified its retailers to remove any remaining recalled product from shelves.

Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it potentially can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life threatening. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. Daily exposure to benzene in the recalled products would not be expected to cause adverse health consequences according to an independent health assessment using established exposure modeling guidelines.

Importantly, no other batches of Hair & Scalp (either before or after these batch codes) and no other Banana Boat products are in the scope of this recall and may continue to be used by consumers safely and as intended.

UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20016AF, Expiration: December 2022, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20084BF, Expiration: February 2023, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 21139AF, Expiration: April 2024, Size: 6 oz

The voluntarily recalled sunscreen spray products are packaged in aerosol cans. Banana Boat will also offer reimbursement for consumers who have purchased a product marked with one of the lot codes in the table above. Lot codes are located on the bottom of the can. Consumers should stop using the affected product immediately and appropriately discard.

In case you experienced 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.

Company name: Edgewell Personal Care Company
Brand name: Banana Boat
Product recalled: Hair & scalp sunscreen spray
Reason of the recall: Due to presence of benzene
FDA Recall date: July 29, 2022

Source: fda.gov
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Wilbur’s of Maine Chocolate Confections of Freeport, Maine is recalling its 8 oz resealable package of milk chocolate covered blueberries because they may contain undeclared chocolate covered almonds. People who have allergies to almonds run the risk of serious or life-threatening allergic reaction if they consume these... See More products. The recalled Milk Chocolate Blueberries were distributed throughout New England, in retail stores, and nationwide through mail orders. No illnesses have been reported to date in connection with this problem.

The product comes in Wilbur’s branded 8-ounce, resealable zippered pouch bag, with UPC # 81321300430 and an expiration date of April 5, 2023 stamped on the backside.

The recall was initiated after a customer discovered chocolate covered almonds in a package (of milk chocolate covered blueberries). The blueberry packaging does not reveal the presence of almonds. Consumers with nut allergies, who have purchased 8 oz packages of milk chocolate covered blueberries, with the best by date of 4/5/23, are encouraged to return them to place of purchase for a full refund.

Subsequent investigation indicates that the problem was caused by a temporary breakdown in the company’s packaging process. The process has been corrected and the company has instituted additional safety checks and corrective actions.

In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Wilbur’s of Maine Chocolate Confections
Brand name: Milk chocolate covered blueberries
Product recalled: Milk chocolate covered blueberries
Reason of the recall: Undeclared almonds
FDA Recall date: July 28, 2022

Source: fda.gov
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The CFIA announced the recall of raw frozen Primal Patties for Dogs Beef Formula because it may be contaminated with Listeria monocytogenes, posing a risk of cross-contamination and illness after handling the pet food. This product was sold in British Columbia. As of August 2, 2022, the... See More company has not received any reports of incidents or illness in Canada.

The recalled product is:
- Primal Patties – Beef Formula, 6 lb, Case UPC: 854495006173, Unit UPC: 850334004164, Lot code number: W10068709, Best by date: 05/22/23.

The lot code number and best by date can be found on the back of the product packaging above the Primal Pet Foods Inc. red oval logo. Only lot code number W10068709 is included is this recall.

Animals that become infected with Listeria monocytogenes could display symptoms similar to humans. Listeria monocytogenes can affect animals eating the product, and there is risk to humans from handling the products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to the products.

Consumers should immediately stop using the recalled product and dispose of the product.

In case you are experiencing Listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, 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. If symptoms persist, seek medical care.

Source: recalls-rappels.canada.ca
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Niagara Region Public Health's beach monitoring program operates annually from Victoria Day to Labour Day. The goal of is to reduce the risk of illness and injury associated with attending the beach. As of August 04, 2022, the Niagara Region Public Health has flagged 4 beaches as... See More unsafe for swimming.

These beaches are:
- Bernard Avenue Beach in Fort Erie is unsafe to swim in due to E. Coli.
- Waverly Beach in Fort Erie is unsafe to swim in due to algae.
- Centennial Cedar Bay Beach in Port Colborne is unsafe to swim in due to algae.
- Nelles Beach in Grimsby is unsafe to swim in due to safety issues.

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The Washtenaw County Health Department and the Washtenaw County Parks and Recreation Commission announced that Independence Lake beach has been closed for swimming the due to high levels of E. coli bacteria. The beach will reopen once follow-up tests confirm levels are low enough to safely swim... See More again.

According to the news this is the third time officials have closed Independence Lake beach this summer due to high levels of E. coli bacteria

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Ultra Supplement LLC is voluntarily recalling lot number DAP272109, exp 4/1/26 of Sustango capsules packaged in 10-count blisters packaged in a carton to the consumer level. Ultra Supplement was notified by Amazon that laboratory analysis has found the product to be tainted with tadalafil, an ingredient in... See More FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com nationwide in the USA. To date, Ultra Supplement has not received any reports of adverse events related to this recall.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.

The presence of tadalafil in Sustango makes this product an unapproved drug for which the safety and efficacy has not been established and therefore, subject to recall.

Consumers with underlying medical issues who take Sustango capsules with undeclared tadalafil may experience health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. The product is marketed as a dietary supplement for male enhancement and is packaged in 10-count blisters packaged in a carton, ASIN X0024468I9. The affected cartons include Lot DAP272109, Exp. 4/1/26. The product can be identified by the label below.

Ultra Supplement is notifying its distributors and customers by this press announcement and by Amazon Messaging and is arranging for return of all recalled products. Consumers that have Sustango capsules Lot# DAP272109 should stop using the product.

In case you experienced 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.

Company name: Ultra Supplement LLC
Brand name: Sustango
Product recalled: Dietary Supplement for Male Enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 25, 2022

Source: fda.gov
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