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Covid-19 OSHA Complaint, Tri-County Metropolitan Transportation District, 4012 SE 17th Ave, Portland, OR 97202, USA

November 18, 2020 12:00 PM

4012 Southeast 17th Avenue, Portland, 97202 Oregon, United States

Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-07-01

Reported By SafelyHQ.com User

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“Violations of the following OSHA standards at the Montefiore Moses, Weiler, Westchester Square, Hutchinson Medical Center, or Montefiore Medical Center clinics: 1904 Failure to provide OSHA 300 Logs of Work-Related Injuries and Illnesses requested by the New York State Nurses Association on Friday,... See MoreApril 10th, 2020. 1910.132 No written, certified hazard assessment for COVID-10 is available. Fit testing is not being conducted on the types of respirators provided to staff to ensure a proper fit and seal. Nurses providing direct care to patients with confirmed COVID-19 are provided with gowns that are not fluid-resistant or impermeable and do not fully cover the back of the wearer. In addition, only one gown is provided per nurse per day, which creates additional infection control risk as the viral load on the gown becomes very high. Nurses are given one face shield per day and are told to clean them. The excessive use and cleaning process sometimes cause the face shield to break apart. Staff are not given access to additional face shields in a timely manner. This even includes nurses who are performing aerosol-generating procedures such as intubation on patients with confirmed COVID-19. Inconsistent or no training is provided to staff regarding safe donning and doffing of Personal Protective Equipment (PPE). Some receive video training, some receive text messages, and some receive no training at all. 1910.134 Staff are not being fit tested on the N95 respirators currently being provided. Montefiore does not have a range of sizes and types of respirators available. The 3M model 1860 N95 respirator currently being provided to nurses is causing medical reactions in many wearers including headaches, skin irritation and skin infections. Montefiore is not conducting safe procedures for discarding and cleaning disposable respirators that are in compliance with manufacturer instructions. 3M and other disposable respirator manufactures have stated that there is no proven method to safely decontaminate disposable respirator models while maintaining the fit and integrity of the respirator. In one facility a garbage bag is hanging on a wall with a sign that says, "Dispose of N95s here." It is not clear what is happening with those used respirators. Other nurses are being told that they must submit their disposable respirator to be auto-cleaned each day. This cleaning will be conducted 5 times and then a new respirator will be issued. Again, no form of cleaning/decontaminating disposable N95s has been approved by disposable respirator manufacturers. 1910.1030 Section 5(a)(1) Staff are not being provided with "clean" (uncontaminated) spaces to eat and drink during their shifts.


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Recent Interesting Reports

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
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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
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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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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
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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
Reported By SafelyHQ.com User

November 12, 2020 12:00 PM

“Additional 1 employees confirmed positive for Covid-19 at AM-1 Roofing in Deschutes County. Investigation Start Date: 10/28/2020 , with the most recent onset of: 10/26/2020 New Cases of: 1

Source: www.oregon.gov See Less
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Covid-19 OSHA Complaint, South Hills Gastroenterology, 825 North Gibson Road, Henderson, NV 89074, USA

South Hills Gastroenterology, 825 North Gibson Road, Henderson, NV 89074, USA

November 18, 2020 12:00 PM

“1. The employer is not providing employees with face masks in efforts to prevent the spread of Covid-19. 2. The employer is not following the Governor's Covid-19 guidelines in regards to enforcing social distancing among employees. Hazard location: Throughout the facility. 07/10/2020 DG

Alleged H... See Moreazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-10
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 1200 N Central Ave, Glendale, CA 91202, United States

Ralphs, 1200 N Central Ave, Glendale, CA 91202, United States

November 18, 2020 12:00 PM

“T8CCR 3203(a) - No temperature screening for employees. No social distancing. Cashiers do not wash their hands frequently and are not cleaning belts. Bathrooms are not cleaned frequently.

Alleged Hazards: 4, Employees Exposed: 25
Source: Osha.gov | Receipt Date: 2020-09-03 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, GTM Stores, 1462 Corporate Center Drive, San Diego, CA 92154, USA

GTM Stores, 1462 Corporate Center Drive, San Diego, CA 92154, USA

November 25, 2020 12:00 PM

“T8 CCR 3203(a)(6) / T8 CCR 3362(a) Several employees have been diagnosed with COVID-19. Employer is not sanitizing surfaces where COVID-19 positive employees were working prior to getting sick. Employees work in groups of 11-15 and have to work next to each other. Employer does not enforce social di... See Morestancing. Employer is not enforcing mandatory face covering for all employees. Forklift operators and drivers are observed in work areas not wearing face covering.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-09-17
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Sneaky Pete's, 16851 U.S. Highway 280, Chelsea, AL 35043, USA

Sneaky Pete's, 16851 U.S. Highway 280, Chelsea, AL 35043, USA

November 10, 2020 12:00 PM

“Employees at the front counter, kitchen, food prep area have been exposed to the COVID-19 virus due to the employer not following Center for Disease Control (CDC) and Alabama Department of Public Health (ADPH) guidelines such as the employer not requiring social distancing as well as not requiring f... See Moreacemasks to be worn.

Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-10-20
See Less
Reported By SafelyHQ.com User