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Dakota's Roadhouse of Jackson, 451 McCarty Lane, JACKSON, OH, 45640, USA
Latest report: April 1, 2021 12:00 PM
OC
Covid-19 OSHA Complaint
1 year ago
The employer has not taken the appropriate steps to protect employees from SARS-C0V-2, the virus that causes COVID-19. The employer does not instruct workers who are infected or potentially infected to stay home and isolate or quarantine, does not isolate workers who show symptoms at work.
Alleged... See More Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-03-15 See Less
68
TT
Employee test positive for Covid-19
2 years ago
A staffer at Dakota's Roadhouse in Jackson tested positive for COVID-19
Source: thetelegramnews.com See Less
68
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Recent Interesting Reports
Salmonella Outbreak Linked to Small Turtles, USA
2 weeks ago
The CDC announced that they are currently investigating a multistate outbreak of Salmonella Stanley infections linked to Small Turtles. As of July 19, 2022, a total of 15 people infected with the outbreak strain of Salmonella Stanley have been reported from 11 states (FL, IA, KS, MA,... See More NY, OH, PA, SC, TN, VA and WA), of the 12 people with information available, 5 (42%) have been hospitalized and no deaths have been reported. Illnesses started on dates ranging from January 3, 2022, to June 24, 2022.
Many people in this outbreak reported purchasing turtles with shells less than 4 inches long from online stores before getting sick. Three people in this outbreak purchased their turtles from a website called myturtlestore.com. The same strain of Salmonella making people sick in this outbreak was also found on turtles purchased from myturtlestore.com.
Pet turtles of any size can carry Salmonella germs in their droppings even if they look healthy and clean. These germs can easily spread to their bodies, tank water, and anything in the area where they live and roam. You can get sick from touching your turtle or anything in its environment and then touching your mouth or food with unwashed hands and swallowing Salmonella germs.
Do not buy small turtles with shells less than 4 inches long. A federal law bans the sale of these small turtles as pets, because they have caused many Salmonella outbreaks, but they are sometimes available for sale online and at stores, flea markets, and roadside stands.
The CDC advises always taking these steps to stay healthy around your pet turtle:
- Always wash hands thoroughly with soap and water right after touching or feeding your turtle and after touching or cleaning the area where it lives and roams.
- Don’t kiss or snuggle your turtle, and don’t eat or drink around it. This can spread Salmonella germs to your mouth and make you sick.
- Keep your turtle out of your kitchen and other areas where you eat, store, or prepare food.
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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.
Source: cdc.gov See Less
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DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to the consumer level. FDA analysis has found the product to contain undeclared sildenafil. Sildenafil is a phosphodiesterase (PDE-5) inhibitor found in FDA-approved... See More products for the treatment of male erectile dysfunction. The presence of sildenafil in SANGTER makes it an unapproved new drug for which the safety and efficacy has not been established and, therefore subject to recall. To date, DISTRIBUTOR RFR, LLC. has not received any reports of adverse events related to this recall.
The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in a 7-count blister pack within a carton, UPC 0 705632 523285, and was distributed through retail stores in the state of Florida from 02/01/2002 to 07/20/2022 and Nationwide in the USA through our website from 02/01/2002 to 07/20/2022 www.sangter.com.
Distributor RFR, LLC is notifying its distributors and customers through this notice and is arranging for the return of all recalled products. All customers are urged to stop consuming the product marked with this lot, and to contact their physician or health care provider if they have experienced any problems that may be related to taking or using this medication.
Risk Statement: Use of SANGTER with undeclared sildenafil may pose a threat to consumers because it 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 these products, adult males who use nitrates for cardiac conditions are at the most at risk from these products.
Company name: Distributor RFR, LLC
Brand name: SANGTER
Product recalled: SANGTER Energy Supplement, 3000mg
Reason of the recall: Undeclared Sildenafil
FDA Recall date: August 02, 2022
Source: fda.gov See Less
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Magnesium Citrate Saline Laxative Oral Solution - recalled due to microbial contamination, USA
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Vi-Jon, LLC is revising a previously reported list of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry that were voluntarily recalled to the consumer level to include product that was distributed in the United States, Canada and Panama. This includes all lots of Cherry... See More Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution, 10 FL OZ (296 mL) within expiry. To date, Vi-Jon, LLC is aware of 3 (three) reports of serious adverse reactions potentially related to this recall. Vi-Jon, LLC is in the process of investigating these reports.
On July 14, 2022, Vi-Jon, LLC recalled all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry. The recall was initiated after Vi-Jon, LLCs third party microbial testing identified the presence of Gluconacetobacter liquefaciens.
Risk Statement: Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences. The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle. In addition to the lemon flavor, the recall includes the Cherry flavor and Grape flavor.
On August 3, 2022, the Recall product list has been updated to include the products noted below.
CANADA Equate Canada 300 mL Lemon Magnesium Citrate
NPN # NPN 80015316
UPC # 079068004923
CANADA Life 300 mL Lemon Magnesium Citrat
NPN # NPN 80015316
UPC # 057800856412
CANADA Life 300 mL Cherry Magnesium Citrate
NPN # NPN 80015316
UPC # 057800856405
CANADA Personnelle 300 mL Lemon Citrate
NPN # NPN 80015316
UPC # 055989029306
PANAMA CRUZ BLANC 10OZ LEMON MAG CIT
NPN # N/A
UPC # 308697403082
The product was distributed in the United States, Canada and Panama to wholesale and retail outlets. Vi-Jon, LLC is continuing their investigation into the cause of the problem.
Vi-Jon, LLC is notifying its customers by phone and email and is arranging for return or destruction of all recalled product. Consumers that have this recalled product should stop using and return any remaining product to the place of purchase.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experienced harm from these products, 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: Vi-Jon, LLC
Brand name: Multiple brand names
Product recalled: Magnesium Citrate Saline Laxative Oral Solution
Reason of the recall: Microbial contamination with Gluconacetobacter liquefaciens
FDA Recall date: August 04, 2022
Source: fda.gov See Less
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Confections Milk chocolate covered blueberries - recalled due to undeclared almonds, USA
2 weeks ago
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 See Less
458
Pfizer Propofol Injection Emulsion, USP - recalled due to Potential presence of visible particulate, USA
4 weeks ago
Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), 100 mL Single Patient Use Glass Fliptop Vial; lot DX9067, to the user level due to a visible particulate observed in a single vial during annual examination of retain... See More samples. The product lot was distributed nationwide to wholesalers/ hospitals/Department of Defense in the United States from June 10, 2020 through June 26, 2020.
The recalled product is:
- Propofol Injectable Emulsion, USP 100 mL Single Patient Use Glass Fliptop Vial, NDC: Vial: 0409-4699-54 Carton: 0409-4699-24, Lot Number: DX9067, Expiration Date Presentation: 01 MAY 2023, Configuration/Count: 1 g/100 mL, Single Patient Use Glass Fliptop Vial Case of 10 Units.
Risk Statement: Patients receiving the impacted product are at risk of experiencing life-threatening adverse clinical effects including but not limited to: blockage of blood vessels, including decreased blood flow to the brain, heart attack, pulmonary embolus, and tissue necrosis. Hypersensitivity reactions and transmission of infectious disease can also occur.
To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for this lot. Propofol is an intravenous general anesthetic and sedation drug for use in the induction and maintenance of anesthesia or sedation. Propofol Injectable Emulsion, USP is a terminally sterilized (TS) product. It is a sterile, nonpyrogenic emulsion containing 10 mg/mL of propofol suitable for intravenous administration supplied in a single patient use fliptop vial.
Wholesalers or hospitals with an existing inventory of the lot, which is being recalled, should stop use and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or hospital level/institution, please notify any accounts or additional locations which may have received the recalled product from you. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.
Company name: Hospira Inc, A Pfizer Company
Brand name: Hospira
Product recalled: Propofol Injection Emulsion, USP
Reason of the recall: Potential presence of visible particulate
FDA Recall date: July 13, 2022
Source: fda.gov See Less
458
Vi-Jon, LLC Magnesium Citrate Saline Laxative Oral Solution - recalled due to bacterial contamination, USA
2 weeks ago
Smyrna, TN, Vi-Jon, LLC is expanding its voluntary recall to include all lots of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry to the consumer level. This expansion includes all lots of Cherry Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution,... See More 10 FL OZ (296 mL) within expiry. On July 14, 2022, Vi-Jon, LLC recalled all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry. The product was distributed Nationwide to wholesale and retail outlets. To date, Vi-Jon, LLC is aware of 3 (three) reports of serious adverse reactions potentially related to this recall.
Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences. The recall was initiated after Vi-Jon, LLCs third party microbial testing identified the presence of Gluconacetobacter liquefaciens. Vi-Jon, LLC is continuing their investigation into the cause of the problem.
The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle. In addition to the lemon flavor, the recall now includes the Cherry flavor and Grape flavor noted below in the table in bold print. Affected Brand, NDC #, UPC # information are listed in the link below.
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: Vi-Jon, LLC
Brand name: Multiple Brands
Product recalled: Magnesium Citrate Saline Laxative Oral Solution
Reason of the recall: Potential Gluconacetobacter liquefaciens contamination
FDA Recall date: July 26, 2022
Source: fda.gov See Less
458
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