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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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Product: Orange

Updated: June 29, 2020 7:47 AM

June 29, 2020 7:47 AM

“Found piece of Plastic in Whole Foods Icecream. Reported the issue to Whole Foods on Jun 7th, but not sure if they are making any effort to recall the product.
UPC: 099482478209
Batch or lot code: 12-25-2020
Product name: 365 Everyday value, ... See More/chocolate#scroll" title="Product: Chocolate">Chocolate Valencia Orange Icecream See Less
Reported By SafelyHQ.com User

June 27, 2020 10:00 AM

“Company name: Saniderm Products
Brand name: Saniderm
Product recalled: Advanced Hand Sanitizer
Reason of the recall: May contain methanol (wood alcohol)
FDA Recall date: June 27, 2020
Recall details: Saniderm Products (Saniderm) is voluntarily recalling Saniderm Advanced Hand Sanitizer, packag ... See Moreed in 1-liter bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol). To date, Saniderm has not received any reports of adverse events related to the product in question.

In response to a recent news alert by the Food and Drug Administration advising consumers of potentially toxic hand sanitizer manufactured by Eskbiochem SA de CV in Mexico, Saniderm has proactively taken necessary precautions to ensure the safety of consumers. Out of an abundance of caution, Saniderm has initiated a voluntary recall of all products produced by Eskbiochem SA de CV with a “Made in Mexico” origin.

The product is a hand sanitizer and is packaged in 1-liter plastic bottles with an orange twist-top cap. The affected Sandiderm Advanced Hand Sanitizer include lot number 53131626, manufactured date April/1/20, clear bottle that can be further distinguished by looking at the back side label and identifying “Made in Mexico” and “Produced by: Eskbiochem SA de CV”. No other bottles distributed by Saniderm match the description above, hence all products as described above are subject to the voluntary recall. The product can be identified by the photos below. The product was distributed in Virginia, Maryland, and New Jersey on April 15,2020.

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.”

Saniderm is notifying its distributors and customers by email and is arranging for the handling of all voluntary recalled products. All individuals that have the bottle in question should immediately stop using and contact Saniderm for guidance on the return and disposal of the product. Consumers with questions regarding this voluntary recall can contact Saniderm at +1 (415) 562-5502‬ or info@sanidermproducts.com from Monday-Friday 9am-6pm, PST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to 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

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Employee test positive for Covid-19, Whitey's Fish Camp, 2032 County Rd 220, Fleming Island, FL 32003, USA

Whitey's Fish Camp, 2032 County Rd 220, Fleming Island, FL 32003, USA

June 23, 2020 12:00 PM

“An employee at Whitey’s Fish Camp in Orange Park has tested positive for COVID-19. The person returned only ... See Moreworked June 14.

Source: actionnewsjax.com
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Reported By SafelyHQ.com User

Employee test positive for COVID-19, Aunt Catfish's On the River, 4009 Halifax Dr, Port Orange, FL 32127, USA

Aunt Catfish's On the River, 4009 Halifax Dr, Port Orange, FL 32127, USA

June 17, 2020 12:00 PM

“An employee at Aunt Catfish’s on the River in Port Orange has tested positive for the coronavirus

Source: news-journalonline.com See Less
Reported By SafelyHQ.com User

May 11, 2020 6:00 PM

“Company name: MasterPharm, LLC
Brand name: MasterPharm, LLC
Product recalled: Finasteride Plus 1.25mg, capsules
Reason of the recall: Contains undeclared minoxidil
FDA Recall date: May 11, 2020
Recall details: MasterPharm, LLC. is voluntarily recalling 1 lot of Finasteride Plus 1.25mg, capsules ... See Moreto the consumer level. The Finasteride Plus capsules have been found to contain undeclared minoxidil, an antihypertensive drug, at levels greater than those found in FDA approved products. The undeclared minoxidil was found when tested with an independent testing laboratory.

Risk Statement: Consumption of undeclared minoxidil would be expected to result in low blood pressure, rapid heartbeat, and salt and water retention causing swelling. Consequently, patients may be at risk of developing heart failure or other heart damage. Excess fluid between the heart and the sac surrounding the heart has also been reported in association with minoxidil use. MasterPharm, LLC. has received 33 reports of increased heart rate, retention of water, dizziness, and low blood pressure.

The product is a compounded drug for hair loss and is packaged in orange prescription bottles containing 30 capsules or blue prescription bottles containing 90 capsules. The affected Finasteride Plus 1.25mg lots include the following 02-27-2020:04@11 and a Beyond Use Date of August 25, 2020. The product can be identified by the patient-specific labeled prescription bottles with product batch labels and a patient-specific prescription label. Finasteride Plus 1.25mg was distributed Nationwide on a patient-specific prescription basis only.

MasterPharm, LLC. is notifying its customers by telephone, e-mail, and common carrier letters and is arranging for return and replacement of all recalled products. Consumers that have Finasteride Plus 1.25mg which is being recalled should stop using and return the Finasteride Plus 1.25mg to MasterPharm, LLC. self-addressed packaging from MasterPharm, LLC. that has been sent to all customers previously. 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

April 21, 2020 12:00 PM

“An employee at Trader Joe’s market on Tustin in Orange, CA has tested positive for COVID-19. The employee was last inside the store on Friday April the 17th.

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

March 10, 2020 9:29 AM

“8 suspected cases - MAR-06-2020 Source: orangeville.com See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

July 9, 2020 11:32 AM

“I’ve never been served a raw pizza like I was served a raw chicken sandwich See Less
Reported By SafelyHQ.com User

July 22, 2020 11:37 AM

“Decided to go to there The food was undercooked. See Less
Reported By SafelyHQ.com User

July 28, 2020 2:00 AM

“Company name: Resource Recovery & Trading, LLC
Brand name: Resource Recover & Trading, LLC
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol subpotency ethyl alcohol
FDA Recall date: July 27, 2020
Recall details: RESOURCE RECOVERY & TRADING LLC, is voluntarily recalling ... See Moreall the lots manufactured by MXL Comercial S.A. de C.V. of Hand Sanitizer with the next information: HAND SANITIZER 70% Ethyl Alcohol Disinfectant Gel, packaged in 6.7 FL Oz. (200 ml) bottles, UPC 650240026020 and HAND SANITIZER Non-sterile Solution 70% Topical Solution, packaged in 20L (5.28 Gal) liter plastic containers, UPC 37710600013 to the consumer level. The products are being recalled due to the potential presence of undeclared methanol (wood alcohol) and subpotency ethyl alcohol.

Risk Statement: The main concern with the use of hand sanitizer that is sub-potent for ethyl alcohol is the potential for decreased bactericidal and virucidal activity. Adverse health consequences can be related to increased infections. In addition substantial, undeclared methanol exposure, which has inferior antiseptic properties compared to ethanol, 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, RESOURCE RECOVERY & TRADING LLC has not received any reports of adverse events related to this recall. The product is used as a hand sanitizer to decrease germs when soap and water is not available and is packaged in 200 ml plastic bottles and 20 liter plastic containers. The product can be identified by the label attached. The product was distribution between June 10, 2020 and June 20, 2020 in the states of Alabama and Georgia.

RESOURCE RECOVERY & TRADING LLC is notifying its distributors and customers by phone calls and emails and is arranging for return and destruction of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using products, initiate recalls to the user level, and return all products to the 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.

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

July 16, 2020 5:32 PM

“gotta love getting raw chicken from here! absolutely shocking! at least i won’t be dying from covid...i’ll be dying from salmonella instead See Less
Reported By SafelyHQ.com User

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.
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Reported By SafelyHQ.com User

June 23, 2020 8:01 PM

“Company name: Golden Nutrition Inc.
Brand name: Golden Nutrition Inc.
Product recalled: Anti-Viral Immune Enhancement Capsules
Reason of the recall: Unsubstantiated Health Claims on Label
FDA Recall date: June 23, 2020
Recall details: Golden Nutrition Inc. of Opa Locka, Florida is recalling fou ... See Morer (4) Lots of Anti-Viral Immune Enhancement Capsules because the label makes unsubstantiated health claims. The recalled Anti-Viral Immune Enhancement were distributed to distributors through orders. The distribution is in Puerto Rico where consumers are able to get the product via retailers.

The product of 60 capsules comes in a green 150cc PET Bottle, with a gold cap marked with lot and expiration number on the bottom of the bottle. The Lot and expiration numbers that are being recalled are the following: Lot:1493 with Expiration: 04/2023, Lot:1499 with Expiration: 04/2023, Lot:1513 with Expiration:05/2023, and Lot:1515 with Expiration 05/2023.  

No illnesses have been reported to date in connection with this problem.

The noncompliance with FDA regulations for label claims was noted after one of our distributors brought it to our attention. The label makes unsubstantiated health claims that the product “helps fight corona virus and influenza.” Consumers that use this product instead of seeking medical treatment run the risk of serious, life threatening health consequences. The production of the product has been suspended while the company works to correct the label. Consumers who have purchased the Anti-Viral Immune Enhancement are urged to return them to the place of purchase for a full refund.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

June 29, 2020 2:01 PM

“Company name: UVT, INC.
Brand name: Saniderm
Product recalled: Advanced Hand Sanitizer, 70% alcohol content
Reason of the recall: Potential presence of methanol (wood alcohol)
FDA Recall date: June 29, 2020
Recall details: UVT, INC. is voluntarily recalling 38,830 liters of SANIDERM ADVANCED H ... See MoreAND SANITIZER, packaged in 1-liter bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol) To date, UVT, INC. has not received any reports of adverse events related to this recall.

The affected SANIDERM ADVANCED HAND SANITIZER includes lot number 0530, Expiration date 04/2022. The product can be identified by the label below. The product was distributed Nationwide in the United States. The product is used as a hand sanitizer and is packaged in 1-liter plastic bottles.

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.

UVT, INC. is notifying its distributors and customers by phone calls, emails and letter and is arranging for replacement and destruction of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using products, initiate recalls to the user level, and return all products to the place of purchase.

Consumers with questions regarding this recall can contact UVT, INC. by phone (951) 427- 3108 or e-mail to customerservice@uvt.world Monday to Friday from 9:00 am and 3:00 pm Pacific Time. 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. 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
Reported By SafelyHQ.com User

July 23, 2020 11:37 AM

“my fiancee was served this raw chicken burger at your restaurant. She noticed it was raw halfway through. Very upsetting and disgusting. See Less
Reported By SafelyHQ.com User

Trader Joe's, 2986 N Eagle Rd, Meridian, ID, United States, Trader Joe's, 2986 N Eagle Rd, Meridian, ID, United States

Symptoms: Nausea Vomiting Cramps Stomach Pain
Trader Joe's, 2986 N Eagle Rd, Meridian, ID, United States

July 26, 2020 1:06 PM

“I took their very green capsules and was puking all night and have stomach pains very severe! Hours and hours of cramping and gut wrenching pain See Less
Reported By SafelyHQ.com User

June 5, 2020 9:34 AM

“They ignoring customers and giving us raw chicken. See Less
Reported By SafelyHQ.com User