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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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Yuma Regional Medical Center, 2400 South Avenue A, Yuma, AZ 85364, USA

Total all time reports:  1
Latest report: April 27, 2020 12:00 PM
Three Employees Test Positive For COVID -19, Yuma Regional Medical Center, 2400 South Avenue A, Yuma, AZ 85364, USA

Three Employees Test Positive For COVID -19

April 27, 2020 12:00 PM

“Three Yuma Regional Medical Center employees have tested positive for the coronavirus

Source: kawc.org See Less
Reported By SafelyHQ.com User

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Recent Interesting Reports

July 14, 2020 4:01 PM

“Company name: AAA Cosmetica, S.A. de C.V.
Brand name: bio aaa
Product recalled: Hand Sanitizer
Reason of the recall: Potential Undeclared Methanol Contamination
FDA Recall date: July 14, 2020
Recall details: AAA Cosmética, S.A. de C.V. is voluntarily recalling all lots of bio aaa Advance Hand ... See MoreSanitizer currently in US distribution, packaged in 480 mL bottles, to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol). To date, AAA Cosmética has not received any complaints or adverse event reports related to this recall.

The product is used as a hand sanitizer and it is packaged in 480 mL plastic bottles. The product can be identified by the label below. Product was distributed Nationwide in the United States. AAA Cosmetica is recalling the following bio aaa Advance Hand Sanitizer lots, all of which bear the expiration date of April 2022:

20DF9001 / 20DF9002 / 20DF9003 / 20DF9004 / 20DF9005 / 20DF9006
20DF9007 / 20DF9008 / 20DF9009 / 20DF9010 / 20DF9011 / 20DF9012
20DF9013 / 20DF9014 / 20DF9015 / 20DF9016 / 20DF9017 / 20DF9018
20DF9019 / 20DF9020 / 20DF9021 / 20DF9022

Risk Statement: Substantial methanol exposure could result in nausea, diarrhea, vomiting, severe abdominal pain, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Persons using these products on their hands may be at risk; however young children who accidently ingest them and adolescents and adults who drink these products are most at risk for methanol poisoning.

Check the full recall details on fda.gov

Source: FDA
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“Company name: Biota Biosciences, LLC
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Reason of the recall: Unapproved new drug
FDA Recall date: May 20, 2020
Recall details: Biota Biosciences is voluntarily recalling the followi ... See Moreng lots in the table below of Cannabidiol (CBD) Complex, Curcumin Complex, and Cannabidiol + Curcumin Injectables to the customer level. These injectable products are being recalled because they were marketed without FDA approval. The products claims on our website make these products unapproved new drugs. Further, the products are misbranded because the labeling fails to bear adequate directions for use.

- Product Name: Cannabidiol(CBD)Complex / Strength(mg): 40 / Multiple Dose Vial Size: 10 mL / Lot: 2H071219P / Expiration: 07/12/2021

- Product Name: Cannabidiol(CBD)Complex / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 10102019P / Expiration: 10/10/2021

- Product Name: Curcumin Complex / Strength(mg): 40 / Multiple Dose Vial Size: 10 mL / Lot: 2H071219CCD / Expiration: 07/12/2021

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- Product Name: Cannabidiol + Curcumin / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 10102019PC / Expiration: 10/10/2021

Risk Statement: Unapproved new drugs injected into the bloodstream for which safety and efficacy have not been established could pose a serious risk of harm to users because they bypass many of the body’s natural defenses against toxic ingredients, toxins, or dangerous organisms that can lead to serious and life-threatening conditions such as septicemia or sepsis. Biota Biosciences has not received any reports of adverse events related to this recall.

Risk Statement: Unapproved new drugs injected into the bloodstream for which safety and efficacy have not been established could pose a serious risk of harm to users because they bypass many of the body’s natural defenses against toxic ingredients, toxins, or dangerous organisms that can lead to serious and life-threatening conditions such as septicemia or sepsis. Biota Biosciences has not received any reports of adverse events related to this recall.

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Water Soluble 40mg/10m products can be identified by the labels attached.

Water Soluble 500mg/10m products can be identified by the labels attached.

Check the full recall details on fda.gov

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March 18, 2020 2:36 PM

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

User:
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.

Safelyhq:
Now that you're impacted by coronavirus, do you have any message to people, now that it's something you've experienced personally or any recommendations?

User:
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August 10, 2020 12:37 AM

“Company name: Soluciones Cosmeticas
Brand name: Bersih
Product recalled: Hand Sanitizer Gel
Reason of the recall: Potential Methanol Contamination
FDA Recall date: August 09, 2020
Recall details: Company Announcement Soluciones Cosméticas voluntary recalled all lots of Bersih Hand Sanitizer Gel ... See MoreFragrance Free sold in 16.9 ounce bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol). This release provides additional information about the packaging for the recalled products. Risk Statement: Substantial methanol exposure can 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 accidently 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 Soluciones Cosméticas has not received reports of adverse events related to this recall. The product is used as a hand sanitizer and is packaged in 16.9 ounce plastic clear bottles with blue tops or green tops with UPC Codes 816822026667 or 7503007103178. The lot numbers range from 0100K01 to 0148K01. This product was distributed nationwide to wholesale distributors and retailers. Soluciones Cosméticas is notifying its distributors by voluntary recall letter and consumers via this press release. Consumers that have the product subject to this recall should stop using and either contact Soluciones Cosméticas per the below for disposal instructions or return it to the place of purchase. Consumers with questions regarding this recall can contact Soluciones Cosméticas at  866-912-8410 Monday through Friday 8am to 5pm Eastern Time or by email at bersihrecall6551@stericycle.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product. 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. Complete and submit the report Online
Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Original Press Release FDA updates on hand sanitizers consumers should not use.
Check the full recall details on fda.gov
Source: FDA
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