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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Goodbye! and best wishes in your recovery

Central State Hospital, 10510 La Grange Rd, Louisville, KY 40223, United States

Total all time reports:  1
Latest report: April 14, 2020 12:00 PM
Patients and hospital staff test positive for COVID-19, Central State Hospital, 10510 La Grange Rd, Louisville, KY 40223, United States

Patients and hospital staff test positive for COVID-19

April 14, 2020 12:00 PM

“Central State Hospital confirmed 12 patients and 24 employees have tested positive of COVID-19 and 2 staff members have died from the coronavirus

Source: 13wmaz.com See Less
Reported By SafelyHQ.com User

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“Interview - SafelyHQ User in Malaysia:
This is a first hand account of the coronavirus situation in Malaysia. The user discusses a colleague's mother being infected, tested, and treatment as well as the situation in the country.

User:
All right. I'm located in Petaling Jaya city in Selangor in ... See MoreMalaysia.

Safelyhq:
Okay, thanks. And what's the scenario in, in your case, how has coronavirus impacted, or what's the experience that you've had?

User:
Initially I thought it wasn't that bad because there were the only like 20 cases, so I thought with 20 cases, you actually just heal up then, it explode to about 50 or a hundred cases. And one of those cases actually affected a colleague's mother in my workplace. And so, we were all given the directive to self-quarantine immediately while the office was getting sanitized. The effect it has had, is a little bit surreal to know that it's coming very close, in terms of actually effecting one of the colleagues. But thankfully he has been tested negative so far so that's a good thing. So just after that, just last night or something, our prime minister declared a movement restriction order in that nonessentials services will be closed and things like it. So things are getting serious and we just had two deaths in the country. Two people have been killed by the virus. And that's a pretty profound and the statistics are climbing for us, like almost 700 people are affected by the virus. I do not know what is the full impact of the restriction order. How will it be enforced, whether there'll be any enforcement of the restrictive order. Some private premises have already started closing. There are closure notices everywhere and things like that. We see councils and staff that are issuing notices of which places they're closing, which places they're checking. Even my friend has a small restaurant and he's saying that it's only open for take away. So, it remains to be seen how these will really affect me and the community and things like that.

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Do you know how testing worked for your colleague's mother, if she was able to get successfully tested and how that worked?

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I do have an account of the experience, she checked into the hospital with some fever and they did an initial test on her. The test that she took, it takes two days to have results. So after two days, they knew that was positive and by that time it was like Tuesday or something like that, Tuesday or Wednesday. And then we got the news then I was immediately told to evacuate the office because he was in office on Monday for a few hours so they might be some contamination and things like that. So on the colleague's mother, after the test was done she was warded into the hospital, special ward and was taken care of. And so far only experiencing mild fever and things like that. And after that she was tested a second time and it was still positive. The son is negative, and so far well she still has the virus inside her. Yeah, it's already been two weeks and not this week. So, we are not sure what is going to happen.

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“Company name: Mylan Institutional LLC
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Reason of the recall: Presence of particulate matter
FDA Recall date: July 07, 2020
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Intravenous administration of a solution containing visible particulates could lead to serious adverse events including, but not limited to, local irritation, vasculitis/phlebitis, antigenic or allergic reactions, and microvascular obstruction, including pulmonary embolism. This batch was distributed nationwide to wholesalers and retail pharmacies between April 2020 and May 2020. The recalled batch is as follows:

- NDC #: 67457-813-50
- Material Description: Daptomycin for Injection
- Strength: 500 mg/vial
- Size: 20 mL vial
- Lot No: 7605112
- Expiry: October 2021

Daptomycin for injection is an injectable antibacterial indicated for the treatment of complicated skin and skin structure infections (cSSSI) and staphylococcus aureus bloodstream infections (bacteremia) in adult patients.

Mylan is notifying its distributors and customers by letter and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop use/further distribution or dispensing.

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

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Brand name: Lupin
Product recalled: Metformin Hydrochloride Extended-release Tablets
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FDA Recall date: June 11, 2020
Recall details: Lupin Pharmaceuticals Inc. is voluntarily recalling Met ... See Moreformin Hydrochloride Extended-Release Tablets USP (generic equivalent of Fortamet®), 500mg, lot G901203 to the consumer level. FDA analysis revealed that this lot exceeded the Acceptable Daily Intake Limit for the impurity N-Nitrosodimethylamine (NDMA). To date, Lupin Pharmaceuticals Inc. has not received any reports of adverse events related to this recall.

Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products and vegetables. Metformin Hydrochloride Extended-Release Tablets USP, 500mg is a prescription oral medication indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus. It is packaged in a bottle containing 60 tablets with NDC 68180-336-07. The affected lot of Metformin Hydrochloride Extended-Release Tablets USP, 500mg is included in below table:

- Product Name: Metformin Hydrochloride Extended-Release Tablets USP, 500mg

- NDC: 68180-336-07

- Lot Number: G901203

- Expiration Date: 12/2020

The product can be identified by the NDC and the lot number available on the side of the bottle label. Metformin Hydrochloride Extended-Release Tablets USP, 500mg was distributed nationwide in the USA to wholesalers, distributors, and mail order pharmacies.

Lupin Pharmaceuticals Inc. is notifying its wholesalers, distributors, and mail order pharmacies by phone and through recall notification and is arranging for the return of all the recalled product lot. Patients taking Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, are advised to continue taking their medication and contact their pharmacist, physician, or medical provider for advice regarding an alternative treatment. According to the U.S. Food & Drug Administration, it could be dangerous for patients with this serious condition to stop taking their metformin without first talking to their health care professionals.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

March 19, 2020 2:35 PM

“Lindt & Sprüngli (USA) Inc. of Stratham, New Hampshire, is issuing a voluntary recall of one lot of its Lindt Excellence 85% Cocoa chocolate bars due to the bars being wrapped in the wrong packagi ... See Moreng. The bars are labeled as Excellence 85% Cocoa, but contain Lindt Excellence Dark Caramel Sea Salt bars. Therefore, this product does not contain accurate information about allergens.

Consumers who have a food allergy or have any sensitivity to milk or soy should not consume the product as it could result in a serious or life-threatening allergic reaction.

The recalled Lindt Excellence 85% Cocoa chocolate bars are labeled with Lot Code L5539, a Best Before date of 11-30-2020, and UPC of 3746601645.

For more information go here: fda.gov

Source: FDA
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Reported By SafelyHQ.com User

July 13, 2020 4:00 PM

“Company name: 4e Brands North America
Brand name: Blumen
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: July 13, 2020
Recall details: Company Announcement San Antonio, Texas, 4e Brands North America is voluntarily recalling ten (10) bottle sizes of H ... See Moreand Sanitizers to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol). Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, 4e Brands North America has not received reports of adverse events related to this recall. Recalled Products These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected Hand Sanitizers are packaged in clear plastic bottles. The recalled products are as follows (a full listing of lot numbers in numerical order is included below the chart):
Check the full recall details on fda.gov
Source: FDA
See Less
Reported By SafelyHQ.com User