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Tennessee, United States
Updated: November 22, 2020 12:00 PM
Employee tested positive for Covid-19, MATA (Memphis Area Transit Authority) Headquarters, 1370 Levee Rd, Memphis, TN 38108, United States
MATA (Memphis Area Transit Authority) Headquarters, 1370 Levee Rd, Memphis, TN 38108, United States
November 22, 2020 12:00 PM
“Another employee at the Memphis Area Transit Authority has recently tested positive for COVID-19
Source: fox13memphis.com See Less”
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Six individuals tested positive for Covid-19, Ralph Askins School, Shady Lane, Fayetteville, TN, USA
Ralph Askins School, Shady Lane, Fayetteville, TN, USA
November 22, 2020 12:00 PM
“Two Fayetteville City Schools employee and four students at Ralph Askins School have recently tested positive for COVID-19.
Source: elkvalleytimes.com See Less”
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Covid-19 OSHA Complaint, Bellevue Middle School, 655 Colice Jeanne Rd, Nashville, TN 37221, United States
Bellevue Middle School, 655 Colice Jeanne Rd, Nashville, TN 37221, United States
November 18, 2020 12:00 PM
“An employee who was under quarantine orders from their doctor entered the building for a staff training. The employee had been tested for Covid the previous day and was told to quarantine by the health department until receiving results from the test. The employee knowingly violated the quarantine t... See Moreo attend the training without results from the covid test. The employee's immediate supervisor knew the employee was supposed to be under quarantine and did not turn the employee away upon entering the building. The employee was exposed to staff members and openly told others that the employee was supposed to be under quarantine but violated it to attend the training.
Source: Osha.gov | Receipt Date: 2020-10-23 See Less”
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Covid-19 OSHA Complaint, Sedonabear Inc., 240 East Main Street, Hendersonville, TN 37075, USA
Sedonabear Inc., 240 East Main Street, Hendersonville, TN 37075, USA
November 18, 2020 12:00 PM
“1. Employees are not being protected from potential exposure to COVID-19.
Alleged Hazards: 1, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-10-09 See Less”
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Covid-19 OSHA Complaint, Exedy America Corporation, 2121 Holston Bend Drive, Mascot, TN 37806, USA
Exedy America Corporation, 2121 Holston Bend Drive, Mascot, TN 37806, USA
November 18, 2020 12:00 PM
“The employer is not enforcing measures to protect workers from exposure to SARS-COV-2(COVID-19).
Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-10-28 See Less”
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Covid-19 OSHA Complaint, One Horse Town Entertainment, LLC, 11220 Outlet Drive, Knoxville, TN 37932, USA
One Horse Town Entertainment, LLC, 11220 Outlet Drive, Knoxville, TN 37932, USA
November 18, 2020 12:00 PM
“1. There are no masks being worn in the building except on the dance floor.* 2. Social distancing cannot be maintained because there are too many people inside the building at one time.* *In regards to COVID-19.
Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-09... See More-28 See Less”
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Covid-19 OSHA Complaint, Old Navy - with Curbside Pickup, 4550 Frontage Rd NW, Cleveland, TN 37312, USA
Old Navy - with Curbside Pickup, 4550 Frontage Rd NW, Cleveland, TN 37312, USA
November 18, 2020 12:00 PM
“1) There have been multiple employees test positive for COVID-19 and management is not informing employees who were in close contact with the positive cases.
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-10-28 See Less”
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Covid-19 OSHA Complaint, Marshal Mize Ford, 5348 State Highway 153, Hixson, TN 37343, USA
Marshal Mize Ford, 5348 State Highway 153, Hixson, TN 37343, USA
November 18, 2020 12:00 PM
“1) Employees are not social distancing. 2) Not all employees wear masks at all times. 3) A manager was present in the facility while positive for COVID-19 and was not wearing a mask. 4) Customers are not required to wear masks, exposing employees to COVID-19.
Alleged Hazards: 4, Employees Expose... See Mored: 1
Source: Osha.gov | Receipt Date: 2020-10-27 See Less”
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Covid-19 OSHA Complaint, Total Network Manufacturing, 8005 Volkswagen Drive, Chattanooga, TN 37416, USA
Total Network Manufacturing, 8005 Volkswagen Drive, Chattanooga, TN 37416, USA
November 18, 2020 12:00 PM
“1.) No ergonomic safety rules are applied; there is no warmup stretch routine. 2.) Workers are required to change stations every two hours due to ergonomics, however, the workers are not being rotated as needed. 3.) Quality inspectors have no ergonomic relief and are required to work the same muscle... See Moregroup 12 hours a day, 5-7 days a week. 4.) Employees are standing one foot apart from each other and are not social distancing to prevent the spread of COVID-19. 5.) Work has not been paused or shut-down to deep-clean the facility after employees have tested positive for COVID-19. 6.) Sanitizer is not available. 7.) No COVID-19 rules are being applied, except during inspections.
Source: Osha.gov | Receipt Date: 2020-10-22 See Less”
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Covid-19 OSHA Complaint, Jim 'N Nick's Bar-B-Q, 3068 Mallory Ln, Franklin, TN 37067, USA
Jim 'N Nick's Bar-B-Q, 3068 Mallory Ln, Franklin, TN 37067, USA
November 18, 2020 12:00 PM
“1. The recommended CDC guidelines are not being followed for COVID-19.
Source: Osha.gov | Receipt Date: 2020-10-27 See Less”
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Recent Interesting Reports
They do not report positive COVID cases, In-N-Out Burger Distribution Center, Hamburger Lane, Baldwin Park, CA, USA
In-N-Out Burger Distribution Center, Hamburger Lane, Baldwin Park, CA, USA
October 31, 2020 12:15 AM
“I am a Butcher for the In N Out Meat Department in Baldwin Park. They do not report positive COVID cases. They just recently began social distance. Supervisor and managers and associates are covid positive or with symptoms. One associate has lost his sister to covid. He was never quarantined. In n o... See Moreut burger is responsible for a big part in the spread of the virus all across California. See Less”
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3 people found this review helpful
Walmart Supercentre, Boulevard Maloney Ouest, Gatineau, QC, Canada, Walmart Supercentre, Boulevard Maloney Ouest, Gatineau, QC, Canada
Walmart Supercentre, Boulevard Maloney Ouest, Gatineau, QC, Canada
November 15, 2020 8:18 PM
“They are practically forcing people to put hand sanitizer on their hands even though they are not required to do so. I am allergic to some of the stuff because I don't know what's in their hand sanitizer and my hands got all cracked and chapped. They still practically forced people to do it even tho... See Moreugh there's no law. See Less”
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2 people found this review helpful
November 23, 2020 2:00 PM
“Company name: Fusion Health and Vitality LLC
Brand name: CORE, Immune Boost
Product recalled: CORE essential nutrients and Immune Boost Sublingual Vitamin D3
Reason of the recall: Unapproved new drug
FDA Recall date: November 23, 2020
Recall details: Fusion Health and Vitality LLCis voluntaril... See Morey recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune Boost Labeling was found to contain statements that caused it to become and unapproved new drug under FDA labeling laws. Hordenine HCl is possibly unsafe when taken by mouth. Hordenine HCl might have similar stimulant effects and side effects such as rapid heart rate and high blood pressure.
Fusion Health and Vitality LLC has not received any reports of adverse events related to this recall. Please review the attached photos for identification. We began shipping Core Essential Nutrients on 1/2/2020 and we began shipping Immune Boost Sublingual Vitamin D3 on 4/15/2020. Both products are packaged with labels which prominently display the product name. CORE essential nutrients are found in a dark colored jar, in powdered format.
This product was formulated to mix into a liquid before consumption. The Immune Boost sublingual was packaged in a 2 ounce bottle that came with a sublingual application dropper. Fusion Health and Vitality is notifying its customers by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using it and return it to Fusion Health and Vitality for destruction. Consumers with questions regarding this recall or how to return recalled product can contact Fusion Health and Vitality by calling 1-888-964-5327, 9am to 5pm, Monday Thru Friday, EST. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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October 28, 2020 11:00 AM
“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: October 28, 2020
Recall details: Sunstar Americas, Inc. (SAI) is voluntarily... See Morerecalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 6/30/22 – 9/30/22 (see specific lots below) to the consumer level. This product may be contaminated with the bacteria Burkholderia lata.
Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia. To date, no adverse events have been reported to SAI related to this recall. The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:
- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.
The product can be identified by as shown in the images below: Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.
Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers are detailed in the link below.
Check the full recall details on fda.gov
Source: FDA See Less”
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October 28, 2020 10:00 PM
“Company name: Whole Foods Market
Brand name: Whole Foods Market
Product recalled: Macaroni and Cheese products
Reason of the recall: Undeclared egg
FDA Recall date: October 28, 2020
Recall details: Whole Foods Market is voluntarily recalling select prepared Macaroni & Cheese products from store... See Mores across five states because they contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
The affected products were sold at Whole Foods Market stores in Maryland, New Jersey, Pennsylvania, Virginia and Washington, D.C. The product was sold in plastic containers and in family-style meal kits with Whole Foods Market scale labels in the prepared foods department, available both hot and refrigerated. The product was also available from the chef’s case counter and from Whole Foods Market online and catering menus. The affected products can be identified by the following information. All affected product has been removed from store shelves. No allergic reactions have been reported to date.
- Macaroni & Cheese, chef’s case. Product Code (begins with) M: 286501. Best by 10/28/2020
- Macaroni & Cheese, packaged. Product Code (begins with) M: 263608. Best by 10/27/2020
- Macaroni & Cheese, online and catering. Product Code (begins with) M: 114449 | 109866. Best by 10/23/2020
- Rotisserie Chicken Meals with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 261596 | 261580 | 261590 | 261601 | 261608 | 261616. Best by 10/26/2020
- Fried Chicken Meal with Mac & Cheese, packaged. Product Code (begins with) M: 247257. Best by 10/25/2020
- Fried Chicken Meal with Mac & Cheese, packaged on hot bar. Product Code (begins with) M: 237444. Best by 10/24/2020
- Chicken Rustico Romano Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 241442. Best by 10/28/2020
- Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 299430. Best by 10/28/2020
- BBQ Turkey Meatballs Chef Plate with Mac & Cheese and Green Beans, packaged. Product Code (begins with) M: 241464. Best by 10/28/2020
- Roasted Turkey Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 242019. Best by 10/28/2020
Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.
Check the full recall details on fda.gov
Source: FDA See Less”
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November 9, 2020 5:00 PM
“Company name: Lohxa, LLC
Brand name: Lohxa
Product recalled: Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free
Reason of the recall: May be contaminated with Burkholderia lata
FDA Recall date: November 09, 2020
Recall details: Lohxa, LLC is voluntarily recalling Chlorhexidine Gluconat... See Moree Oral Rinse USP, 0.12% Alcohol free (NDC:70166-027-15) products bearing an expiration date from 01/31/21 – 03/31/21 (see specific lots below) to the consumer level. This product is sourced and repackaged from Sunstar Americas Inc. who has notified us the product may be contaminated with the bacteria Burkholderia lata.
Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia. To date, no adverse events have been reported to Lohxa, LLC related to this recall.
The prescription oral rinse product, available through institutional use only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:
- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free is distributed in cases each containing 50 unit dose cups. Each case contains a colored label around the lid and body of the case.
The product can be identified by as shown in the images below. Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free was distributed to Nationwide to hospital pharmacies. Lohxa, LLC is notifying its direct customers by Fedex overnight mail, electronic mail, phone call and is arranging for return of all recalled products.
Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately. Consumers with questions regarding this recall can contact Lohxa, LLC by phone at 1-800-641-5564 or email info@lohxa.com on Monday-Friday from 8am-5pm EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers follow below:
- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free, 15 mL (NDC:70166-027-15) LOT/ EXP: T09101A/01/2021 |T08292A/02/2021 |T10011A/02/2021 |M10193A/03/2021 |T10223A/03/2021
Check the full recall details on fda.gov
Source: FDA See Less”
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November 19, 2020 6:01 PM
“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi USA
Product recalled: Dexmedetomidine HCL in 0.9% Sodium Chloride Injection
Reason of the recall: Cross Contamination with Lidocaine
FDA Recall date: November 19, 2020
Recall details: Fresenius Kabi USA is voluntarily recalling a singl... See Moree lot of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to a trace amount of lidocaine present in the lot. This recall is being performed to the user level. To date, no adverse drug experience reports have been received for the recalled lot. Administration of Dexmedetomidine HCl containing trace amounts of lidocaine to a patient with lidocaine allergy could result in a potentially life-threatening allergic reaction.
Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection is approved for intravenous use and indicated for sedation of non-intubated patients prior to and/or during surgical and other procedures. Listed below is a table of the recalled lot distributed nationwide to wholesalers, distributors, hospitals and pharmacies between April 9, 2020 and April 13, 2020. An image of the label is also included below.
- Dexmedetomidine HCl in 0.9%. Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL fill in a 50 mL vial. NDC Number: 63323-671-50. Product Code: 671050. Batch number: 6123925. Expiration Date: 03/2022. First Ship Date: 04/09/2020. Last Ship Date: 04/13/2020
Fresenius Kabi is notifying its distributors and customers by letter and asking them to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product.
Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing any affected lots, and to return the product to Fresenius Kabi.
Customers with questions regarding this recall may contact Fresenius Kabi at 1-866-716-2459 Monday through Friday, during the hours of 8:00 a.m. to 5:00 p.m. Central Time. Consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using this drug product.
Check the full recall details on fda.gov
Source: FDA See Less”
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Covid-19 OSHA Complaint, Magnolia Manor, 411 Ansel Street, Greenville, SC 29601, USA
Magnolia Manor, 411 Ansel Street, Greenville, SC 29601, USA
November 10, 2020 12:00 PM
“An employee tested positive for COVID-19. The employer did not test the employees who worked in close proximity with the employees who tested positive.
Source: Osha.gov | Receipt Date: 2020-08-12 See Less”
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Covid-19 OSHA Complaint, SCHOOL DIST #210 KING COUNTY, 4041 S 298th St, Auburn, WA 98001, USA
SCHOOL DIST #210 KING COUNTY, 4041 S 298th St, Auburn, WA 98001, USA
November 18, 2020 12:00 PM
“Employees have tested positive for Covid19 and employees that have been in direct contact are not being informed. Employees are all over the building without a mask.
Source: Osha.gov | Receipt Date: 2020-10-22 See Less”
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2 employees tested positive for Covid-19, Georgia-Pacific Corporation, 17 Kitty Hawk Dr, Santa Teresa, NM, USA
Georgia-Pacific Corporation, 17 Kitty Hawk Dr, Santa Teresa, NM, USA
November 3, 2020 12:00 PM
“Multiple employees(2) at GEORGIA-PACIFIC CORP in SANTA TERESA, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 11/04/2020,
Source: env.nm.gov See Less”
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