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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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Good Samaritan Society - Sioux Falls Village, 3901 S Marion Rd, Sioux Falls, SD 57106, United States

Total all time reports:  1
Latest report: April 21, 2020 12:00 PM
40 people at a Retirement community test positive for COVID-19, Good Samaritan Society - Sioux Falls Village, 3901 S Marion Rd, Sioux Falls, SD 57106, United States

40 people at a Retirement community test positive for COVID-19

April 21, 2020 12:00 PM

“23 residents and 17 employees at the Good Samaritan Society - Sioux Falls Village retirement community have tested positive.

Source: keloland.com See Less
Reported By SafelyHQ.com User

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June 5, 2020 5:00 PM

“Company name: Marksans Pharma Limited, India
Brand name: Time-Cap Labs, Inc.
Product recalled: Metformin Hydrochloride Extended-Release Tablets, USP 500mg
Reason of the recall: Due to detection of N-Nitrosodimethylamine (NDMA)
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Recall details: Marksans Pharma Limi ... See Moreted, India is voluntarily recalling Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004, to the consumer level. FDA analysis has found the product to contain N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit (ADI) of 96ng/day. 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 found in water and foods, including meats, dairy products and vegetables.

Marksans Pharma Limited has not received any reports of adverse events related to this recall to date. Metformin Hydrochloride Extended-Release Tablets, USP 500mg is indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in 100 count bottles with NDC code 49483-623-01. The affected Metformin Hydrochloride Extended-Release Tablets, USP 500mg, are white to off white, capsule shaped, biconvex tablets, debossed with ‘101’ on one side and plain on the other side.

Product name: Metformin Hydrochloride Extended Release Tablets USP, 500 mg
Lot #: XP9004
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The product can be identified by lot # XP9004 and expiration date 12/2020. Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004 was distributed by Time-Cap Labs, Inc. nationwide in the USA to wholesalers who further distributed to pharmacies. Marksans Pharma Limited is notifying its distributors and customers by issuing notification letter and press release and is arranging for return/replacement etc. of recalled product lot.

Distributors/retailers that have Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004 which is being recalled should return to place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug 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

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March 17, 2020 8:43 PM

“Interview - Maroy, Lyon France:
This is a first hand account of the coronavirus situation in Lyon France, including one member of their community that has been diagnosed, and another working in a nearby hospital.

Maroy:
I am 25 and I'm living in Lyon in the east France and it's like the third ... See Moreregion which is the most touched by the virus. And right now I'm at home since Monday the government told us to stay at home, so I'm not touched by the virus, but I know some, an old person who are touched by the virus. And I have a friend who is working in the hospital in the care units and she explained to me what the media is hiding and what's the truth behind this virus.

Safelyhq:
What area does your friend work in the hospital? And what is she seeing?

Maroy:
She's living in the South of France, Toulouse and she's in the care units. So she's working closely with the people who are in the worst situation in the hospital. So she see's a lot of cases everyday and everyday she's told me that it's worse.

Safelyhq:
Some of the materials state that it's mostly older people that are impacted, is that what she's seeing?

Maroy:
So at first in the media, they say that only old people and fragile persons who have a disease are impacted. But now this is not the truth. Now,people who are 23 years old, 25, 30 are impacted.

Safelyhq:
Have you heard anything about testing? Is it hard to get testing or is it easy to get testing?

Maroy:
Yes. One week ago I was talking with my doctor and we were talking about the virus and he told me, you know, we are talking a lot with the other doctors and I can tell you right now that we don't have in France,no testing, no tests anymore. We don't know if a person has a flu, if it's simple flu or the coronavirus and when he told me that I was really anxious because even the doctors can't diagnose now if this only a flu or if it's worse.

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Maroy:
Don't take that too lightly. This is really my word, don't take that too lightly. When I see that in UK, they say that they are counting on the auto immunity of people. I just don't understand. If I have a thing to say it, don't shake hands, don't hug someone, wash your hands carefully, and just take it this really, really seriously. Because this is not a simple flu. It's bigger than that.
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Raw chicken sandwich, Wendy's, Orlando, FL 32827, United States

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April 20, 2020 4:00 PM

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Brand name: Fresenius Kabi
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Reason of the recall: Presence of Particulate Matter
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Recall details: Freseni ... See Moreus Kabi USA, LLC is voluntarily recalling 13 lots of Ketorolac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial and Ketorolac Tromethamine Injection, USP, 60 mg/2 mL (30 mg/mL), 2 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter composed of the following elements: carbon, silicon, oxygen, and polyamides.

Particulate matter was found in eight reserve sample vials. Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.

Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine injection should not exceed 5 days. Listed below is a table of the recalled lots distributed nationwide to wholesalers, distributors, hospitals, and pharmacies between May 5, 2018 and December 16, 2019, as well as a copy of the label:

- Ketorolac Tromethamine Injection, USP, 30 mg / mL, 1 mL fill in a 2 mL amber vial. NDC: 63323-162-01. Product code: 160201. (Check the recall notice for specific batch numbers)
- Ketorolac Tromethamine Injection, USP, 60 mg / 2 mL (30 mg / mL), 2 mL fill in a 2 mL amber vial. NDC: 63323-162-02. Product code: 160202. (Check the recall notice for specific batch numbers)

Check the full recalled product list and details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User