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Product: Ham
Updated: July 8, 2020 12:00 PM
Employee test positive for Covid-19, Livingston Parish Library, Denham Springs-Walker Branch, 8101 U.S. Hwy 190, Denham Springs, LA 70726, United States
Livingston Parish Library, Denham Springs-Walker Branch, 8101 U.S. Hwy 190, Denham Springs, LA 70726, United States
July 8, 2020 12:00 PM
“The Denham Springs/Walker Branch re-closed earlier in the week after an employee at the branch tested positive for COVID-19.
Source: wbrz.com See Less ”
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Employee test positive for Covid-19, Lee's Nails, 389 W State St, Binghamton, NY, USA
Lee's Nails, 389 W State St, Binghamton, NY, USA
July 7, 2020 12:00 PM
“An employee of Lee’s Nail Salon, 389 W. State St. in Binghamton, has tested positive for COVID-19. The Health Department is asking anyone who was in the salon between June 28 and July 3 to self-quarantine for 14 days after the date they were there.
Source: ... See Moretarget='_blank'>pressconnects.com See Less ”
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Employee test positive for Covid-19, Walgreens, 1050 North Main, Chatham, IL 62629, USA
Walgreens, 1050 North Main, Chatham, IL 62629, USA
July 6, 2020 12:00 PM
“An employee at Walgreens on Main Street in Chatham has tested positive for COVID-19. It is unknown when the employee last worked.
Source: newschannel20.com See Less ”
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Employee test positive for Covid-19, Publix Super Market at Post Commons Shopping Center, 4100 North Wickham Road, Melbourne, FL, USA
Publix Super Market at Post Commons Shopping Center, 4100 North Wickham Road, Melbourne, FL, USA
July 5, 2020 12:00 PM
“A Publix employee at the location on 4100 N Wickham Road, Suite 109, Melbourne has tested positive for Covid-19.
Source: floridatoday.com See Less ”
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Publix employee test positive for Covid-19, Publix Super Market at Suntree Square, 7777 N Wickham Rd, Melbourne, FL 32940, United States
Publix Super Market at Suntree Square, 7777 N Wickham Rd, Melbourne, FL 32940, United States
July 5, 2020 12:00 PM
“A Publix employee at the location on 7777 N. Wickham Road, Melbourne has tested positive for Covid-19.
Source: floridatoday.com See Less ”
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Employee test positive for Covid-19, Publix Super Market at Hamlin Cove, 5400 Hamlin Groves Trail, Winter Garden, FL, USA
Publix Super Market at Hamlin Cove, 5400 Hamlin Groves Trail, Winter Garden, FL, USA
July 5, 2020 12:00 PM
“A Publix employee at the location on 5400 Hamlin Groves Trail, Winter Garden has tested positive for Covid-19.
Source: orlandosentinel.com See Less ”
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Employee test positive for Covid-19, United States Postal Service, 309 N Market St, Brenham, TX 77833, United States
United States Postal Service, 309 N Market St, Brenham, TX 77833, United States
July 2, 2020 12:00 PM
“A worker at Brenham post office tested positive for covid-19
Source: kwhi.com See Less ”
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Employee test positive for Covid-19, Blue Bell Creameries Distribution Center, 1101 S Blue Bell Rd, Brenham, TX 77833, United States
Blue Bell Creameries Distribution Center, 1101 S Blue Bell Rd, Brenham, TX 77833, United States
July 1, 2020 12:00 PM
“Another Blue Bell Creameries employee at the Brenham facility tested positive for COVID-19
Source: kwhi.com See Less ”
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Employee test positive for Covid-19, The 57th Fighter Group Restaurant, 3829 Clairmont Rd, Atlanta, GA 30341, USA
The 57th Fighter Group Restaurant, 3829 Clairmont Rd, Atlanta, GA 30341, USA
June 29, 2020 12:00 PM
“An employee at 57th Fighter Group Restaurant in Chamblee has tested positive for Covid-19 on June 3.
Source: atlanta.eater.com See Less ”
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Employee test positive for Covid-19, gusto! Chamblee, 4945 Peachtree Blvd, Chamblee, GA 30341, USA
gusto! Chamblee, 4945 Peachtree Blvd, Chamblee, GA 30341, USA
June 29, 2020 12:00 PM
“Another employee at Gusto at Chastain and in Chamblee has tested positive for Covid-19.
Source: atlanta.eater.com See Less ”
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Recent Interesting Reports
IcelandicPlus LLC Whole Capelin Fish Pet Treats - recalled due to Potential for Clostridium botulinum, Fort Washington, PA, USA
Fort Washington, PA, USA
April 3, 2020 2:00 PM
“Company name: IcelandicPlus LLC
Brand name: Icelandic+
Product recalled: Whole Capelin Fish Pet Treats
Reason of the recall: Potential for Clostridium botulinum
FDA Recall date: March 23, 2020
Recall d ... See Moreetails: Out of an abundance of caution IcelandicPlus LLC of Ft. Washington, PA, is recalling its Capelin Pet Treats because some of the fish have exceeded the FDA compliance guideline for fish larger than 5 inches. The FDA has determined that salt-cured, dried, or fermented un-eviscerated fish larger than 5 inches have been linked to outbreaks of botulism poisoning in humans between 1981 and 1987 and again in 1991. Since some IcelandicPlus Capelins are larger than 5 inches there is a possible health risk. To date there have been no reported illnesses of dogs, cats, or persons in connection with Capelin. Nor has there been any positive test results for Clostridium botulinum from any IcelandicPlus Capelin, but because of the potential risk, and despite no known illnesses in connection with our products, we have decided in co-operation with the FDA, to announce this product recall. Clostridium botulinum toxin can cause severe clinical signs including death in both animals consuming the pet treat and people handling the pet treat or coming in contact with contact areas that have been exposed to the product. Common symptoms may include dizziness, blurred or double vision, trouble with speaking or swallowing, difficulty breathing, muscle weakness, abdominal distension, and constipation. Consider that several of the listed symptoms, such as double vision, cannot be easily assessed in animals or conveyed by an animal. Pets or persons experiencing these symptoms should seek immediate medical attention. The Capelin product was shipped to distributors in the United States with the intent to be sold to Retailers who in turn sell to Consumers. This product would be found in Independent Pet Specialty Stores within all States in the United States. The product comes in a clear plastic package or tube, and marked Icelandic+ Capelin WHOLE FISH, PURE FISH TREATS FOR DOGS, or PURE FISH TREATS FOR CATS UPC CODES, 8 5485400775 9; 8 5485400711 7; and 8 5485400757 5 are packaged in a 2.5 ounce tube or a 1.5 or 2.5 ounce bag (lot numbers 02/2020 to 02/2022)IcelandicPlus is family owned and run by pet parents who take the safety and wellbeing of its consumers and clients with the utmost importance, as such we are conducting this voluntarily recall to further protect our customers. Additionally, we are changing our Capelin supplier to ensure that the fish in our product are consistently less than 5 inches, or if larger, they will be completely eviscerated. Distributors, Retailers and Consumers who have purchased IcelandicPlus’s Capelin can return it to the location where it was purchased for a refund.
Check the full recall details on fda.gov
Source: FDA See Less ”
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2 people found this review helpful
Hardee's, Army Post Road, Des Moines, IA, USA, Hardee's, Army Post Road, Des Moines, IA, USA
Symptoms: Other
Hardee's, Army Post Road, Des Moines, IA, USA
June 5, 2020 8:07 AM
“Foreign objects in coffee. Looked like burger from nose. See Less ”
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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 See Less ”
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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 See Less ”
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Chengdu Ai Qin Colored contact lenses - recalled due to being distributed without FDA clearance, USA
USA
June 24, 2020 6:00 PM
“Company name: Chengdu Ai Qin E-commerce Co., Ltd
Brand name: TTDeye
Product recalled: Colored contact lenses
Reason of the recall: Distributed without FDA clearance may pose health risk
FDA Recall date: June 24, 2020
Recall details: On June 18, 2020, Chengdu Ai Qin E-commerce Co., Ltd initiate ... See Mored a nationwide recall of 1362 pairs of colored contact lenses. The relevant series of contact lenses have been found to be distributed without FDA clearance and may pose a threat to health. The company has received no complaints to date.
These colored contact lenses were sold through the company website and shipped directly to the customer from 08/05/2019 - 10/11/2019. The recalled products were manufactured in August 2018 and may be identified by name of the product and the date of manufacture, “2018-08”, found on the package label. The following products are being recalled:
- TTDeye. Black Starshine. Lot code: B16112100
- TTDeye. Diamonds Starlight. Lot code: B16112203
- TTDeye. Flower. Lot code: Brown. Lot code: B16112210
- TTDeye. Flower Grey. Lot code: B16112231
- TTDeye. Radial. Lot code: Brown. Lot code: B16112109
- TTDeye. Radial Pink. Lot code: B16112110
- TTDeye. Devil Red. Lot code: B16112201
If you have received this product, immediately cease use and contact the company via online chat at www.ttdeye.com between 9AM and 6PM (GMT+8) or contact the company via email at info@ttdeye.com (24 hours) for further information.
Chengdu Ai Qin E-commerce Co., Ltd is notifying its customers by email and is arranging for return/replacement of all recalled colored contact lenses.
Chengdu Ai Qin E-commerce Co., Ltd is voluntarily recalling these contact lenses after becoming aware of the problem. Chengdu Ai Qin E-commerce Co., Ltd has notified the FDA of this action.
Check the full recall details on fda.gov
Source: FDA See Less ”
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KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom, KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom
KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom
May 27, 2020 9:34 AM
“No chips with my meal and pink chicken Face with symbols over mouth Absolutely grim man See Less ”
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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 See Less ”
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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)
FDA Recall date: June 05, 2020
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
Expiry Date (MM/YYYY): 12/2020
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
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 ”
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Interview - SafelyHQ User in Malaysia - Live Account of the Coronavirus Situation, Petaling Jaya, Selangor, Malaysia
Petaling Jaya, Selangor, Malaysia
March 18, 2020 2:36 PM
“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.
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:
Okay. basically just stay away from large crowds. Stay within your own home if possible as much as possible. Only go out if you absolutely need to like get groceries done or get food or things like that, which is basically the aim of this movement control that we are having now. Basically that for individuals, do not travel, interstate or do not travel long distances back to your hometowns or homelands because that might cause the infection amongst other people who are older or elder, it's mostly the elderly people who get affected the most with the underlying conditions. However, one of the deaths in our country, is from a 34 year old men. Who didn't have any preexisting conditions. So that's actually quite scary. For this, I think the advice of staying away from people, and keeping checks on your health and practicing all the hygiene things, washing your hands for 20 seconds, wash up your hands and hand sanitizers and things like that See Less ”
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4 people found this review helpful
Shearer's Foods employee tested positive for COVID-19, Shearer's Snacks, 800 NW 4th St, Perham, MN 56573, USA
Shearer's Snacks, 800 NW 4th St, Perham, MN 56573, USA
April 12, 2020 12:00 PM
“Details: Shearer's Foods confirmed Thursday that an employee in its Perham manufacturing location has tested positive for COVID-19.
The employee has been asked to self-quarantine at home for 14 days and has not come in contact with the product so there is no food safety risk.
Report: 4/10/2020 ... See MoreSource: perhamfocus.com See Less ”
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