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Covid-19 OSHA Complaint, Swickard Corporation, 25035 SW Parkway Ave, Wilsonville, OR 97070, USA

November 18, 2020 12:00 PM

25035 Southwest Parkway Avenue, Wilsonville, 97070 Oregon, United States

Serious

Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-06-10

Reported By SafelyHQ.com User

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Recent Interesting Reports

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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Reported By SafelyHQ.com User

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 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

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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

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November 29, 2020 9:25 PM

“The FSA announced the recall of raw dog food products by Happy Hounds Wales Ltd because they may contain salmonella.

FSA advises consumers not to use the recalled product. Instead, return it to the store from where it was bought for a full refund. When handling and serving raw pet food it is alw... See Moreays advised to clean utensils and feeding bowls thoroughly after use.

- Frozen Beef Kidney (1kg). Batch code: 962. Best before: 10/26/2021
- Frozen Whole Heart (Individual Item). Batch code: 962. Best before: 10/26/2021
- Frozen Chicken and Beef Sleeve (1kg). Batch code: 1344/962. Best before: 11/2/2021
- Frozen Lamb and Beef Sleeve (1kg). Batch code: 962-966. Best before: 11/4/2021
- Frozen Diced Heart (1.5kg). Batch code: 962. Best before: 10/26/2021

Check the full recall details on food.gov.uk

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Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Salmonella

Covid-19 OSHA Complaint, iTow Towing, 23642 Vía Fabricante, Mission Viejo, CA 92691, USA

iTow Towing, 23642 Vía Fabricante, Mission Viejo, CA 92691, USA

November 10, 2020 12:00 PM

“T8 CCR § 3203(a)(2) ¿ Facial coverings mandate not enforced in the workplace. Employees and patrons concerned with potential exposure to Covid-19 at the workplace.

Alleged Hazards: 1, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-10-13 See Less
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Covid-19 OSHA Complaint, Northern Pride Inc, 518 Pennington Ave S, Thief River Falls, MN 56701, United States

Northern Pride Inc, 518 Pennington Ave S, Thief River Falls, MN 56701, United States

November 10, 2020 12:00 PM

“There are at least six positive COVID-19 cases at the facility and the company is not having employees who worked in close proximity to these employees quarantined.


Source: Osha.gov | Receipt Date: 2020-10-19 See Less
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Covid-19 OSHA Complaint, Taste of Sicily, 132 East Main Street, Palmyra, PA 17078, USA

Taste of Sicily, 132 East Main Street, Palmyra, PA 17078, USA

November 10, 2020 12:00 PM

“The employer has not implemented a good infection control plan including things such as face coverings for employees, training, social distancing, etc. Refer to the Centers for Disease Control CDC guidance for employers at this link. cdc.gov... See Morebusinesses-employers.html OSHA in coordination with the Department of Health and Human Services has prepared Guidance on Preparing Workplaces for COVID-19. It can be found here: osha.gov OSHA has Guidance on Returning to Work osha.gov

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-08-03
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Mortenson Construction, 12918 Orange Plank Road, Locust Grove, VA 22508, USA

Mortenson Construction, 12918 Orange Plank Road, Locust Grove, VA 22508, USA

November 18, 2020 12:00 PM

“1. It is alleged employees are reporting to work with symptoms of COVID-19 and are allowed to remain at work. 2. It is alleged employees are not wearing a face covering when working within 6' of others and if they do, it is not being worn properly over both the nose and mouth to prevent the spread o... See Moref COVID-19. The wearing of a facemask is not enforced. 3. It is alleged thin painters plastic is in place in cars, work trucks, vans, etc., and the barriers are becoming contaminated as employees are not cleaning and disinfecting between other groups of employees riding in the vehicles. 4. It is alleged this painter plastic that is in place in vehicles is causing a visibility problem for the drivers. 5. It is alleged the cleaning products being used to sanitize equipment, etc., is so diluted that it does not kill the virus which causes COVID-19. 6. It is alleged employees are congregating together such as in trailers, at picnic tables and are not social distancing.

Alleged Hazards: 6, Employees Exposed: 620
Source: Osha.gov | Receipt Date: 2020-09-29
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Parts Authority Robinwood, 6161 Robinwood Rd, Baltimore, MD 21225, United States

Parts Authority Robinwood, 6161 Robinwood Rd, Baltimore, MD 21225, United States

November 25, 2020 12:00 PM

“Locations - Buildings 6101 and 6161. Possibly employees are exposed to COVID-19 where personal protective equipment (PPE) was not provided. Possibly employees are exposed to COVID-19 where chemicals used for disinfecting was not provided. Possibly employees exposed to electrical hazard as a result o... See Moref temporary wiring used in lieu of permanent wiring. Possibly employees exposed to tripping and struck by hazards as a result of poor housekeeping and low hanging wires. Possibly employees exposed to fall hazards by using ladders unable to reach elevated highs. Possibly employees exposed to inadequate lighting in aisleways. Possibly employees exposed to crushing hazards as a result of the lack of foot protection not required while using carts weighing up to approximately 75 pounds. Possibly employees exposed to egress hazards by possible blocked exits.


Source: Osha.gov | Receipt Date: 2020-05-20
See Less
Reported By SafelyHQ.com User