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County Dublin, Ireland
Updated: April 26, 2020 12:00 PM
Tested positive for coronavirus with no symptoms, South Dublin, County Dublin, Ireland
South Dublin, County Dublin, Ireland
April 26, 2020 12:00 PM
“I tested positive for the coronavirus with 000 symptoms & so did some of my friends!! You can feel completely fine and be positive for the virus but your friends Mam etc could have asthma or a heart condition and will get very very sick!! See Less”
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family friend contracted coronavirus, Dublin, Ireland
Dublin, Ireland
April 3, 2020 12:00 PM
“A very close family friend developed symptoms for COVID-19 and have now tested positive. She is one of the nicest person I know, so please pray for her full recovery? See Less”
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my mom, dad and brother have symptoms of COVID 19, South Dublin, County Dublin, Ireland
South Dublin, County Dublin, Ireland
April 2, 2020 12:00 PM
“My mom, dad, and brother have symptoms of COVID 19. My brother is the only one who was tested and is positive. Drs refuse to test my mom and dad because of the shortage. So who knows that the actual numbers in the USA are for those affected See Less”
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Coronavirus-like symptoms, Dublin, Ireland
Dublin, Ireland
March 11, 2020 8:33 PM
“I literally have all the symptoms of coronavirus and my doctor was like “ur grand” and here I am 2 days later, absolutely not grand See Less”
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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 See Less”
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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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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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5 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, Good Samaritan Hospital, 375 Dixmyth Avenue, Cincinnati, OH 45220, USA
Good Samaritan Hospital, 375 Dixmyth Avenue, Cincinnati, OH 45220, USA
November 25, 2020 12:00 PM
“1. On the 11th A/B floor, COVID-19 positive patients are not being treated in negative pressure rooms. The ventilation intake in the wall is not being vented to the outside. The filters at the intakes are not being changed. These were positive pressure rooms for the immune compromised. Aerosol-gener... See Moreating procedures take place in these rooms 2. On the 11th A/B floor, COVID-19 positive patients have portable ventilators placed in their rooms. The ventilators are venting to the hallway. The filters in the units are not being changed. The filters are not the correct particulate size. The filters have a MERV rating of 8 instead of 16. Employees have not been trained on how to properly handle these units to ensure that negative pressure is being maintained. 3. Employees have to enter the dirty room and bypass dirty personal protective equipment to obtain clean N95 respirators.
Alleged Hazards: 3, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-10-21 See Less”
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1 person found this review helpful
Covid-19 OSHA Complaint, Faurecia Gladstone Plant, 601 South Gladstone Avenue, Columbus, IN 47201, USA
Faurecia Gladstone Plant, 601 South Gladstone Avenue, Columbus, IN 47201, USA
November 25, 2020 12:00 PM
“An employee was around someone who tested positive for covid-19. This was a week ago and still working. Today the employee was sent home to be quarantined. Faurecia did not tell anyone they may have been exposed to it. Employees over heard the union talking about it. The employee was having symptoms... See Moreyesterday and today. Faurecia has not quarantined anyone else and the employee was in close contact with over 20 other employees. Faurecia only cares about parts ans this is putting other employees at risk and thier families. They did not clean anything either the employee was touching.
Source: Osha.gov | Receipt Date: 2020-08-20 See Less”
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Covid-19 OSHA Complaint, McLaughlin Painting, 875 Cinnabar St, San Jose, CA 95126, USA
McLaughlin Painting, 875 Cinnabar St, San Jose, CA 95126, USA
November 18, 2020 12:00 PM
“Potential concern regarding implementing Center for Disease Control (CDC), Local Health Department and Cal/OSHA Guidance on Requirements to Protect Workers from Coronavirus to prevent the spread between person-to-person and close contact (within about 6 feet) while working and enforce wearing of fac... See Moree covering by all employees. Title 8 CCR Sections 3203 & 3380
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-23 See Less”
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Covid-19 OSHA Complaint, Tenneco Automotive, 800 Trey St, Jeffersonville, IN 47130, USA
Tenneco Automotive, 800 Trey St, Jeffersonville, IN 47130, USA
November 10, 2020 12:00 PM
“They are not following COVID-19 guidelines they sat in place to clean between shifts and also let all employees know of confirmed cases. They took seats out from the break room leaving metal poles sticking up from the tables which is an easy trip hazard. They have staggered schedules to keep exposur... See Moree low but they also send people from one line to the next. Today's meeting employees were told that they would be working 12 hour days, 7 days a week until further notice. The factory focus manager said that is was "unusual circumstances" and had nothing to do with customer demand. After talking to other employees in the plant, employees discovered that they sent 22 people home. They took them one by one outside and told them to go get tested and not come back until the results are negative. It was also discovered that two team leads have contracted COVID-19. The factory focus manager did not discuss any further information about the reason for such a drastic schedule change. He also stated that he cannot give employees any more information. Employees pieced together that many more have came into contact with these two team leads and possibly the entire 3rd shift. A group lead just last week went to 3rd shift to cover for another group lead out on vacation. Employees are all extremely worried for their health and the health of their families as they will be in contact with each other constantly until further notice.
Source: Osha.gov | Receipt Date: 2020-07-16 See Less”
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Covid-19 OSHA Complaint, Michaels, 540 Frandor Ave, Lansing, MI 48912, USA
Michaels, 540 Frandor Ave, Lansing, MI 48912, USA
November 10, 2020 12:00 PM
“1. The employer does not disinfect high touch surfaces such as shopping carts, doors, or PIN input pads at registers. 2. Employees are not aware if there is a response plan. 3. A symptom self-questionnaire log is not kept, nor has one ever been kept. Employees are only asked to self-report a tempera... See Moreture scan when an employee punches in on site, with no direction to report any symptoms to management. 4. An employee recently tested positive for COVID, and it is unknown if this was reported to the health department or to coworkers who may have been in contact with the employee. 5. Employees are not aware if there is a designated COVID safety coordinator on site. 6. On 10/16 the "mask required for entry signage" was taken down, and it is unsure if there are plans to replace this it. Frequently the requirement is not enforced within the store when customers come in without a mask. 7. Basic rules are not followed across the store as whole, and similar violations took place under the rescinded Governor's orders.
Source: Osha.gov | Receipt Date: 2020-10-19 See Less”
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