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Illinois, United States
Updated: November 25, 2020 12:00 PM
Covid-19 OSHA Complaint, Herscher High School, 501 N Main St, Herscher, IL 60941, USA
Herscher High School, 501 N Main St, Herscher, IL 60941, USA
November 25, 2020 12:00 PM
“I work at Bonfield Grade School as a paraprofessional in Herscher Community Unit School District #2. Starting last week, a child in the classroom that I work in was told to quarantine for two weeks because their mother tested positive for COVID-19. Early this week, another child from my classroom wa... See Mores sent home to quarantine because their parent tested positive. On Thursday, we were told about a third child in our class who had a parent that tested positive and is now on quarantine. This particular child was at school on Monday. As of today, 10/30, an entire class was sent home to quarantine because of a positive case in the classroom, EXCEPT the para professionals. Those para professionals were expected to continue to come to school and work the after school program like they normally do. This is putting our entire staff and students at risk of exposure. There has been no formal notifications to staff regarding positive cases, and specifically, none about the direct contact I¿ve had with COVID in my own classroom.
Source: Osha.gov | Receipt Date: 2020-10-30 See Less”
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Covid-19 OSHA Complaint, Northwest Special Recreation Association (NWSRA), 3000 W Central Rd, Rolling Meadows, IL 60008, United States
Northwest Special Recreation Association (NWSRA), 3000 W Central Rd, Rolling Meadows, IL 60008, United States
November 25, 2020 12:00 PM
“Employer has not been disclosing when an employee has tested positive with COVID-19 until days later. Approx. 6 people have tested positive, and the staff is expected to resume regular duties, even if directly exposed to those 6 people. The employer refuse to close down and offer options to work fro... See Morem home during an exposure/quarantine period. Certain employees are required to quarantine after traveling to different states or participating in events, while others are not required, with similar circumstances. The employees at NWSRA are forced to work regardless of exposure, which in turn, leads to exposing high risk participants within each program. NWSRA has not been consistent in cleaning and disinfecting and have not enforced exposure protocols, putting all lives at risk.
Alleged Hazards: 1, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-10-23 See Less”
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Covid-19 OSHA Complaint, University of Illinois Hospital & Health Sciences System, West Taylor Street, Chicago, IL, USA
University of Illinois Hospital & Health Sciences System, West Taylor Street, Chicago, IL, USA
November 25, 2020 12:00 PM
“Not provided opportunity to work remote. Unable to properly social distance in area due to employee spacing. Two employees test positive for COV 19 and co-workers not informed.
Source: Osha.gov | Receipt Date: 2020-10-20 See Less”
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Covid-19 OSHA Complaint, 9th District Chicago Police Department, 3120 S Halsted St, Chicago, IL 60608, United States
9th District Chicago Police Department, 3120 S Halsted St, Chicago, IL 60608, United States
November 25, 2020 12:00 PM
“COVID Health and Safety measures are not being enforced. Majority of employees in the building do not follow IDPH guidance on mask. Others who work in my workspace refuse to wear face coverings per IDPH guidance. Employer's quarantine does not follow IDPH guidance.
Source: Osha.gov | Receipt D... See Moreate: 2020-10-20 See Less”
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Covid-19 OSHA Complaint, Chicago Police Department, West Grand Avenue, Chicago, IL, USA
Chicago Police Department, West Grand Avenue, Chicago, IL, USA
November 25, 2020 12:00 PM
“Personal protective equipment (PPE) is not being distributed to employees at the 5555 W GRAND AVE location to prevent the spread of Covid-19. The PPE is being restricted by front office staff without a legitimate reason.
Source: Osha.gov | Receipt Date: 2020-10-13 See Less”
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Covid-19 OSHA Complaint, Shawnee Alliance, 6355 Brandhorst Dr, Carterville, IL 62918, USA
Shawnee Alliance, 6355 Brandhorst Dr, Carterville, IL 62918, USA
November 25, 2020 12:00 PM
“Not proper PPE or cleaning supplies for COVID-19
Source: Osha.gov | Receipt Date: 2020-08-13 See Less”
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Covid-19 OSHA Complaint, Domestics, Etc. (2nd Location in the Quincy Mall), 119 North 6th Street, Quincy, IL 62301, USA
Domestics, Etc. (2nd Location in the Quincy Mall), 119 North 6th Street, Quincy, IL 62301, USA
November 25, 2020 12:00 PM
“1. Employees are exposed to illnesses including coronavirus and the employer has not implemented distancing, barriers or required the use of masks covering the nose and mouth. 2. Employees are exposed to illnesses including coronavirus and the employer does not ensure shared surfaces are cleaned wit... See Moreh an EPA registered sterilant between different employee use.
Alleged Hazards: 2, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-10-30 See Less”
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Covid-19 OSHA Complaint, thyssenkrupp Presta Danville, LLC, 75 Walz Creek Dr, Danville, IL 61834, United States
thyssenkrupp Presta Danville, LLC, 75 Walz Creek Dr, Danville, IL 61834, United States
November 25, 2020 12:00 PM
“Employees are exposed to illnesses including coronavirus and the employer is not ensuring the work stations are cleaned with an EPA registered sterilant between shifts.
Alleged Hazards: 1, Employees Exposed: 25
Source: Osha.gov | Receipt Date: 2020-10-30 See Less”
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Covid-19 OSHA Complaint, Green Certified West, 2541 W Iles Ave, Springfield, IL 62704, USA
Green Certified West, 2541 W Iles Ave, Springfield, IL 62704, USA
November 25, 2020 12:00 PM
“1. Employees working upstairs are exposed illnesses including coronavirus and the employer does not ensure that workers practice distancing. 2. Employees working upstairs are exposed illnesses including coronavirus and the employer does not ensure the work surfaces are cleaned daily with an EPA appr... See Moreoved disinfectant.
Alleged Hazards: 2, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-10-20 See Less”
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Covid-19 OSHA Complaint, Triton Manufacturing Co. Inc, 5700 West Triton Way, Monee, IL 60449, USA
Triton Manufacturing Co. Inc, 5700 West Triton Way, Monee, IL 60449, USA
November 25, 2020 12:00 PM
“1. The employer is not following CDC guidelines in regarding informing employees of workers who have tested positive for Covid-19. Four employee(s) tested positive and the coworkers were not informed . Applicable OSHA standard(s): Section 5(a)(1) General Duty Clause of the Occupational Safety and He... See Morealth Act of 1970
Source: Osha.gov | Receipt Date: 2020-11-10 See Less”
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Recent Interesting Reports
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 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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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 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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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
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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Covid-19 OSHA Complaint, SLG Construction, 149 Church Street, New York, NY 10007, USA
SLG Construction, 149 Church Street, New York, NY 10007, USA
November 18, 2020 12:00 PM
“Complainant alleges the following: 1. Employees are not provided with proper and sufficient quantities of PPE. The employer is not providing N-95 respirators or nitrile gloves to employees while working. 2. Employees have to reuse N-95 respirators due to a limited supply. 3. Complainant is had conta... See Morect with an individual that tested positive for COVID-19 and requested a N-95 respirator to prevent potentially spreading the virus.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-06-01 See Less”
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Covid-19 OSHA Complaint, Michigan Milk Producers Association, 125 Depot St, Constantine, MI 49042, USA
Michigan Milk Producers Association, 125 Depot St, Constantine, MI 49042, USA
November 10, 2020 12:00 PM
“1. Numerous employees are refusing to wear masks on the grounds they have a medical condition. The employer has been made aware and has instructed employees to contact human resources to receive a face shield as an alternative to a face mask. This appears to be only enforced or encouraged by some ma... See Morenagement. 2. The employer has posted signs informing milk haulers they are required to wear a mask, but this isn't being followed either. This is especially concerning because they are traveling between farms and plants and coming into contact with a lot of people multiple times a day. 3. Symptoms of Covid-19 are still being ignored by management unless a doctor tells you not to go to work or you have a fever over 100.4. Employees are still expected to report to work, and will be written up for calling in for headaches, diarrhea, sore throats etc.
Source: Osha.gov | Receipt Date: 2020-08-19 See Less”
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Covid-19 OSHA Complaint, El Torito Drive-In Deli, 1116 South Standard Avenue, Santa Ana, CA 92701, USA
El Torito Drive-In Deli, 1116 South Standard Avenue, Santa Ana, CA 92701, USA
November 25, 2020 12:00 PM
“T8 CCR § 3203 (a)(6) ¿ Facial coverings order not enforced in the workplace. Employees and customers not wearing facial coverings.
Alleged Hazards: 1, Employees Exposed: 3
Source: Osha.gov | Receipt Date: 2020-10-20 See Less”
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