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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

Peter D Clark Centre Long Term Care, 9 Meridian Pl, Nepean, ON K2G 6P8, Canada

Total all time reports:  1
Latest report: May 5, 2020 12:00 PM
3 people at the nursing home have test positive for COVID -19, Peter D Clark Centre Long Term Care, 9 Meridian Pl, Nepean, ON K2G 6P8, Canada

3 people at the nursing home have test positive for COVID -19

May 5, 2020 12:00 PM

“Two residents and an employee at the Peter D. Clark Centre nursing home test positive for COVID -19.

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

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August 5, 2020 12:36 AM

“Company name: Roque Plast S.A. de C.V.
Brand name: Command Brands
Product recalled: Hand Sanitizer
Reason of the recall: Methanol Contamination
FDA Recall date: August 04, 2020
Recall details: Roque Plast S.A. de C.V. is voluntarily recalling lots 200371-12, 200371OH-05, 170420OH-06, 170420OH-8 ... See Moremanufactured by Roque Plast S.A. de C.V. of Command Brands Gel AntiBac Instant Hand Sanitizer to the consumer level. This recall has been initiated due purported potential presence of methanol indicated by the Food and Drug Administration (FDA) when product was presented for import in the United States. Although, final official FDA analysis results and reports have not been received, out to the abundance of caution and as suggested by the FDA, Roque Plast S.A. de C.V. are recalling lots 200371-12, 200371OH-05,170420OH-06,170420OH-8.

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 Roque Plast S.A. de C.V. has not received reports of adverse events related to the products of this recall.

Recalled Products:
Name product: Command Brands Gel AntiBac Instant Hand Sanitizer
NDC: 50058-100-08
Package formats (sizes):  8.4 fl oz (250 mL)
Plastic bottleUPC: 8_52239_00689_2
Affected lot (numbers):  200371-12, 200371OH-05, 170420OH-06, 170420OH-8

The product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The products are packaged in an 8.4 fl oz (250 mL) PET or High-density polyethylene (HDPE) plastic bottle with UPC 8_52239_00689_2. The product is labeled with a red, blue and yellow stripes with the words Command Brands Gel AntiBac Instant Hand Sanitizer written in yellow and blue letters. The product was distributed nationwide throughout the United States.

Roque Plast S.A. de C.V. is notifying its customers/distributors by recall letter and consumers via this press release.  We are also notifying our distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled products.

Consumers, distributors, and retailers that have product which is being recalled should stop use or distribution and return to place of purchase. Consumers should contact their physician or healthcare provider if they experienced any problems that may be related to taking or using this product.

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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July 13, 2020 4:00 PM

“Company name: 4e Brands North America
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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
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Reported By SafelyHQ.com User

I was Rushed to the hospital for a bad allergic reaction, Bubba Gump Shrimp Co., Las Vegas Boulevard South, Las Vegas, NV, USA

Symptoms: Diarrhea Nausea Vomiting Other
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July 14, 2020 12:51 PM

“I was Rushed to the hospital for a bad allergic reaction & they refuse to refund.

They were informed of my food allergies before ordering. They messed up my order twice and informed me that there was no tomatoes or jalapeños ... See Moreitle="Product: Pepper">peppers in the remade dishes but I still had an allergic reaction to the food. No could tell me if the dish was prepared separate, with clean, uncontaminated utensils. If the cook changed his gloves before pairing my food or if he'd touch tomatoes or jalapeños when preparing my dish or card to answer any of my questions. The response was, "well we made a knew dish. I don't know what happened." No one took responsibility.

The the staff were not trained to respond in a food allergy emergency. My tongue, lips and throat swelled. The waiter gave me water and ice, I took benadryl, then began vomiting the contaminated food. My friend and another customer had to get help and tell the manager to call 911. The manager comped one dish and made My friend pay the bill before the ambulance took me to the hospital.

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Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Urgent Care

March 21, 2020 3:19 PM

“Interview - Doctor in Paris, France:
This is a first-hand account from a SafelyHQ user that is a medical professional on the coronavirus situation in France. She discusses how her work has changed since the start of the pandemic, work rotations and testing for medical professionals, and issues faci ... See Moreng patients and medical professionals.

Charlotte:
I'm a pediatric resident and I work in a pediatric hospital. I was working in the genetics unit and it's mostly outpatient and non-intensive care, so we were actually closed down last week. Just because most of us are pediatricians and so we were kind of needed elsewhere. So I decided to stop working because of my pregnancy. But then all my other colleagues are still working and they're actually now, at home, confined at home and they're waiting to be called to different departments are probably either the ER or intensive care unit and from what they understand for now, they just have to stay home and rest. And they're going to be called out probably next week when the first wave of doctors start being a little tired, probably hospitalized because they themselves are sick. So right now they're mostly, resting at home. And then I know that our unit, so was shut down and a lot of other non-urgent care at our hospital was shut down and everything is being reorganized so that we have Covid units. And so at the hospital I work in, is actually a pediatric hospital, but they're going to open an adult Covid unit just because obviously adults are more affected than children are.

SafelyHQ:
Are there any changes as a pediatrician?

Charlotte:
In most maternity at least in Paris, the dads aren't allowed in the delivery room or in the hospital at all for now. So things are pretty rough on new moms right now. And I know that we're also kind of being slowly prepared that we're probably not going to be able to have an epidural just because there won't be any doctors available. So, getting prepared for maybe a rough delivery for most new moms right now, at least new Parisian moms.

SafelyHQ:
Is testing easy for people to get so far or has it been a problem for some people. And how do things look like on that front?

Charlotte:
So, in our hospital it's very easy for all medical, staff if they have any of the symptoms to get tested. It's very, very easy. I know that for patients we only test patients that are unstable or in very critical care. Just because we can't afford to test everyone, but staff is definitely prioritized and we're all told we can get tested as easily if we want to. Or if I mean, not if you want to obviously if you have symptoms.

SafelyHQ:
Did you know anyone who has got diagnosed with coronavirus?

Charlotte:
Yeah, actually, I already have a couple of friends who are staying at home because they have it. One of my, well actually he is also a pediatric resident is at home right now with, well he's getting tested today, but it's most likely Covid. His wife was tested and got tested positive after having a five day fever. And now he has a fever since yesterday, so he did his test today. So very, very likely, also Covid positive. And so his wife is also a medical resident who probably got it working at the ER and then he got it through her.

SafelyHQ:
Being in the medical field and seeing what, the medical field is doing in France and learning about, about coronavirus. And having some friends who have it, do you have any, messages that you, they have for people who want to learn more?

Charlotte:
I think just the best thing is to stay informed on what's happening on reliable sites because I know there's a lot of misinformation out there and just do what they can to stay home. Because the big wave is going to come. And I know all my friends in the hospitals are getting as ready as they can, but I'm sure you've heard that there already some parts of France that are in a very, very complicated situation where they're already out of machines for like life support machines and out of room in intensive care units. And so hopefully Paris doesn't get there, but we never know. And it all kind of just relies on people really being careful and staying home and I know everyone wants to go outside to buy their bread and whatever, but it's always a risk. And just be mindful that, yeah, doctors are doing the best they can. And I know I have friends that are pharmacist and other things like that that are complaining because they don't have masks or they're not protected. But the truth is doctors rarely have mask as well, and everyone's of kind of going through it as they can and doing the best they can. So yeah, that's the message. I think just relax, stay at home and know that everyone is trying to get organized and do the best they can, and it's obviously not perfect, but it is what it is for now.
See Less
Reported By SafelyHQ.com User

June 1, 2020 6:00 PM

“Company name: Amneal Pharmaceuticals LLC
Brand name: Amneal
Product recalled: Metformin Hydrochloride Extended-Release Tablets, USP 500mg and 750mg
Reason of the recall: Due to detection of N-Nitrosodimethylamine (NDMA)
FDA Recall date: June 01, 2020
Recall details: Amneal Pharmaceuticals L ... See MoreLC Bridgewater, New Jersey (Amneal), is voluntarily recalling all lots of Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, within expiry to the Retail Level. Amneal was notified by the U.S. FDA that the Agency’s testing of seven lots of Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, showed N-Nitrosodimethylamine (NDMA) amounts above acceptable FDA levels.

FDA recommended the recall of the seven tested lots. Amneal has agreed to this recall and has further decided to extend the recall to all lots within expiry of Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, out of an abundance of caution. Further scientific evaluations are ongoing at Amneal. To date, Amneal has not received any reports of adverse events that have been confirmed to be directly related to this recall. Amneal’s Metformin Hydrochloride Immediate Release Tablets, USP are not affected by 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 found in water and foods, including meats, dairy products, and vegetables. Metformin HCl Extended-Release Tablets, USP, 500 mg and 750 mg, manufactured by Amneal, are prescription, solid oral products that are indicated as an adjunct to diet and exercise to improve blood sugar control in adults with type 2 diabetes mellitus. The Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, subject to the recall, are identified by the NDC numbers stated on the product label.

Metformin HCl Extended-Release Tablets, USP, 500 mg
53746-178-01. 100 count bottles
53746-178-05. 500 count bottles
53746-178-10. 1000 count bottles
53746-178-90. 90 count bottles
53746-178-Bulk. Bulk Box
65162-178-09. 90 count bottles
65162-178-10. 100 count bottles
65162-178-11. 1000 count bottles
65162-178-50. 500 count bottles

Metformin HCl Extended-Release Tablets, USP, 750 mg
53746-179-01. 1000 count bottles
53746-179-Bulk. Bulk Box
65162-179-10. 100 count bottles

The affected Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, lots were distributed nationwide in the US directly to Wholesalers, Distributors, Retailers, and Repackagers.

Amneal is notifying its direct customers via mail (UPS Standard Overnight) by mailing a recall notification letter and is arranging for the return of all the recalled products. Anyone with an existing inventory of the product should quarantine the recalled lots immediately.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

April 20, 2020 6:00 PM

“Company name: Braun Medical Inc
Brand name: B. Braun
Product recalled: Ceftazidime for Injection USP (2g) and Dextrose for Injection USP (50 ml) in Duplex® Container
Reason of the recall: Out-of-Specification Results for High Molecular Weight Polymers
FDA Recall date: April 20, 2020
Recall de ... See Moretails: Braun Medical Inc. (B. Braun) is voluntarily recalling one (1) lot of 2g Ceftazidime for Injection USP (2g) and Dextrose for Injection USP (50 ml) in Duplex® Container to the hospital/user level.. During stability testing of Batch H8J812, test results were found to exceed the specification limits for High Molecular Weight Polymers (HMWP) at the nineteen (19) month [82 week] stability interval. Elevated levels of High Molecular Weight Polymers have been shown to cause kidney damage and liver issues in animal studies. While the impact of HMWP in humans is unknown, B. Braun is initiating this voluntary recall out of an abundance of caution to prevent any risks of adverse reactions due to the elevated HMWP levels.

To date there have been no complaints or reports of adverse reactions associated with this product lot. Ceftazidime for Injection USP and Dextrose Injection USP is a cephalosporin antibacterial indicated in the treatment of the following infections caused by susceptible isolates of the designated microorganisms: Lower respiratory tract infections; skin and skin-structure infections; bacterial septicemia; bone and joint infections; gynecologic infections; intra-abdominal infections; and central nervous system infections.

Ceftazidime for Injection USP and Dextrose Injection USP in the DUPLEX® Container is a flexible dual chamber container containing approximately 50 mL of 5% Dextrose Injection in the diluent chamber and ceftazidime in the drug powder chamber. After reconstitution, the concentration is equivalent to 2 g ceftazidime. Ceftazidime for Injection USP and Dextrose Injection USP is packaged in 24 DUPLEX® Containers per case. The affected recalled product includes the following lot number and expiration date:

- NDC: 0264-3145-11. Ref: 3145-11. Dose/Volume: 2 g per 50 mL. Impacted batch: H8J812. Exp. Date: 31 Jul 2020.

Product was distributed Nationwide within the United States to domestic distributors. Pictures of the product and product labeling follow this press release.

B. Braun is notifying its distributors and customers by an official recall notice sent via certified registered mail and is arranging for return of all recalled products. Facilities and distributors that have product which is being recalled should discontinue use immediately and contact the B. Braun Medical Inc. Customer Support Department

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

July 6, 2020 11:30 PM

“Company name: J. M. Smucker Company
Brand name: Natural Balance
Product recalled: Ultra Premium Chicken & Liver Paté Formula
Reason of the recall: Due to elevated levels of choline chloride
FDA R ... See Moreecall date: July 03, 2020
Recall details: The J. M. Smucker Company today announced a voluntary recall of one lot of Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food due to health concerns likely associated with elevated levels of choline chloride. Ingesting impacted product may cause nausea with excessive salivation, constricted pupils and poor vision, diarrhea or vomiting to more severe symptoms including difficulty walking, muscle shaking, tremors, irregular heartbeat, difficulty breathing, possible cardiac or respiratory failure and, in extreme situations, death. Pet parents are encouraged to contact their cat’s veterinarian immediately if their cat is displaying any of these symptoms.

If pet parents have any product matching the following description in their possession, they should stop feeding it to their cats and dispose of the product. This information can be found on the bottom of each can.

- Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food (5.5 oz). UPC: 2363353227. Lot code: 9217803. Best by: 08 04 2021

These products are most commonly sold in pet specialty retailers and online throughout the United States and Canada. No other Natural Balance® products are impacted by this recall.

The Company has received reports of adverse reactions. Pet parents that have questions or would like to report adverse reactions should call 888-569-6828, Monday through Friday, 8 a.m. – 5 p.m. ET or email anytime at info@naturalbalanceinc.com.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User