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Harper's Restaurant & Brewpub, 131 Albert St, East Lansing, MI 48823, United States
14 people that visited have test positive for Covid-19
3 years ago
14 people have tested positive for COVID-19 after recently visiting Harper's Restaurant & Brewpub in downtown East Lansing. If you visited between June 12 - June 20 to watch for symptoms.
Papa johns is not protecting their employees from COVID, Papa Johns Pizza, 9123 N Loop 1604 W, San Antonio, TX 78249, United States
3 months ago
Papa johns is not protecting their employees from COVID. I just got COVID and strep tested and it came back positive for both. They immediately told me to come back to work. This is completely unsanitary and unsafe for employees and customers. They are not following protocols... due COVID -19 and are disregarding everything just to have the correct amount of staffing.
I started feeling symptoms yesterday morning after eating at this location in Dunn. The location was very dirty and none of the people wore masks. I have had to cancel my driver's test, dentist appointment, doctor's appointment and several other events. | Symptoms: Other
I was staying at a shelter in Lockport Cares and there was a Christian pastor at the shelter. Guess again. I dialed an ubulanxe to go to the hospital because my teeth were bleeding.and I was coughing up blood. The woman told me I should not stay... at Lockport Cares because I called an ambulance to go to the hospital.
I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.
For 2 nights there is always corn or brownies during Bible study at 8pm at night.
I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.
My blood sugar was low and I was coughing up blood and my teeth were bleeding.
Warning. Lockport Cares does food poisoning
Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
You are not required to wear mask indoors.amd of you are positive for covid 19, you are not required to wear a mask. There is a woman positive for covid 10 not wearing a mask everyday spreading her disease. Lockport Cares allows kids and married couples to stay the night also.
Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.
Warning. | Symptoms: Cough
11 months ago
Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, their molecular, over-the-counter test used to identify SARS-CoV-2 (the virus that causes Covid-19) in self-collected nasal swabs. The recall affects a total of 11,102 tests shipped to customers from July 26th, 2022 through August 26th,... 2022. The test was granted Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) on October 28, 2021. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution.
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. The reliability of positive test results is not affected.
Below is a list of the affected lots. The lot number can be found on the side of each test box along with the Use By date.
Lot Number: HB264, Use By Date: 1/1/2023, Number of Tests Shipped: 7,382
Lot Number: HY263, Use By Date: 1/1/2023, Number of Tests Shipped: 1,800
Lot Number: HY264, Use By Date: 1/1/2023, Number of Tests Shipped: 1,920
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution. The reliability of positive test results is not affected.
Detect is notifying all customers and distributors affected by the recall. Anyone in possession of any unused tests from the affected lots should dispose of the tests. The outer packaging is recyclable while all the test components can be discarded as regular trash. Detect Hubs are not affected by the recall and do not need to be discarded.
Test users who attempt to use recalled tests will be notified in the Detect App™ that the test has been recalled and may not be used.
Detect, Inc. will issue a refund* for the affected tests (as verified by Detect) upon customers’ acknowledgement of receipt of the recall-related communication and confirmation that any affected tests in possession have been disposed of.
Company name: Detect, Inc.
Brand name: Detect
Product recalled: Over the counter Covid-19 Test
Reason of the recall: There is an increased chance that the tests from the lot numbers listed below may give false negative results
FDA Recall date: December 12, 2022
11 months ago
We presumed we had bad food but it turned out to be the latest covid variant. Extreme stomach pain and headache, along with bad bowel and bitter mouth. Not like the extreme fatigue and sinus of the last few rounds of SARS-Co-V-2. There was an issue with... chorizo fat in a breakfast burrito that added to it, however that was not the main culprit, just difficult to digest (apparently for many). A tasty evil. Currently in California | Symptoms: Headache, Fatigue, Stomach Pain
1 month ago
Nearly 1,500 Lansing Board of Water & Light customers are currently affected by a power outage. According to BWL’s Outage Map, the cause has not been determined yet.
Outage link: outages.lbwl.com
5 months ago
As of 2:30 p.m. Thursday, power had been restored to affected areas of East Lansing and Meridian Township. Nearly 2,000 Consumers Energy customers in East Lansing and Meridian Township were out of power as of 12:30 p.m. on Thursday afternoon.The Consumers Energy Outage Map showed the impacted... areas being between Park Lake and Abbot roads, north of Haslett Road and some of the area north of Lake Lansing Road. The Jackson-based electric utility company said trees were to blame for the disruption.
Consumers Energy: consumersenergy.com
Jackson Electric: outagemap.jacksonemc.com
5 months ago
Around 6,604 Consumers Energy customers in Lansing are without power, the energy company reports. The outage is mostly contained to the East Lansing, DeWitt and Bath areas, with some outages creeping into Lansing proper.
Outage link: consumersenergy.com
1 year ago
Thousands of Lansing Board of Water & Light customers lost electrical service Friday after a utility pole caught fire in East Lansing. At one point, more than 4,000 customers were without power
Outage link: outages.lbwl.com
Published: 2022 02 11
Recent Interesting Reports
4 weeks ago
Cardinal Health, Inc. is initiating a voluntarily recall for all lots of ophthalmic products supplied by Velocity Pharma, LLC to the consumer level. Cardinal Health, Inc. received information from FDA indicating investigators found insanitary conditions in the manufacturing facility and positive bacterial test results from environmental sampling... of critical drug production areas in the facility. Products were distributed Nationwide to Wholesalers and Retailers starting December 12, 2021. To date, Cardinal Health, Inc., and its subsidiaries have received reports of three (3) adverse events related to these products. The reports of adverse events were shared with their supplier, Velocity Pharma, LLC.
The recalled products are:
- LEADER™ Eye Irritation Relief (Polyvinyl Alcohol, 0.5%, Povidone, 0.6%, and Tetrahydrozoline Hydrochloride, 0.05%), 0.5 FL OZ bottle (15 mL), NDC:
- LEADER™ Dry Eye Relief (Carboxymethylcellulose Sodium, 1%), 0.5 FL OZ bottle (15 mL), NDC: 70000-0089-1
- LEADER™ Lubricant Eye Drops (Carboxymethylcellulose Sodium, 0.5%), 0.5 FL OZ bottle (15 mL). NDC: 70000-0090-1
- LEADER™ Lubricant Eye Drops (Carboxymethylcellulose Sodium, 0.5%), 2 bottles, 0.5 FL OZ (15 mL) each. NDC: 70000-0090-2 (Carton) 70000-0090-1 (Bottle)
- LEADER™ Dry Eye Relief (Polyethylene Glycol 400, 0.4% and Propylene Glycol, 0.3%), 0.33 FL OZ bottle (10 mL), NDC: 70000-0088-1
- LEADER™ Lubricant Eye Drops (Propylene Glycol, 0.6%) 0.33 FL OZ bottle (10 mL), NDC:70000-0587-1
These products are available as over the counter (OTC) products used for temporary relief of burning and irritation due to dryness of the eye, for use as a protectant against further irritation or to relieve dryness of the eye, and/or to relieve redness of the eye due to minor eye irritations.
Risk Statement: For those patients who use these products, there is a potential risk of eye infections that could result in partial vision loss or blindness. These products are intended to be sterile. Ophthalmic drug products pose a potential heightened risk of harm to users because drug applied to the eyes bypass some of the body’s natural defenses.
Wholesalers, Distributors and Retailers that have the affected product which is being recalled should cease distribution of the products. Consumers should stop using the recalled eye drop products and may return them to the place of purchase.
In case you experience harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Cardinal Health, Inc.
Brand name: LEADER
Product recalled: OTC Ophthalmic Sterile Drops
Reason of the recall: Insanitary manufacturing conditions
FDA Recall date: November 01, 2023
Received a package from "Jane" at 371 Little Falls Rd Unit 4 Cedar Grove, NJ. 07009. 2 "Trump" Coins - 1 "gold", 1 "silver". Never ordered anything from Jane and would NEVER order a Trump anything.
TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder - recalled due to presence of benzene, USA
6 days ago
Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company (“Insight”), is voluntarily recalling two lots of TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder to the consumer level. A recent review by our manufacturer and their third-party lab found that samples from two lots of the... product contained elevated levels of benzene. The affected lots were distributed nationwide in the United States through a limited number of retailers and online. To date, the Company has not received any serious adverse events related to this recall.
Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it potentially can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Insight is recalling these products out of an abundance of caution. Benzene is ubiquitous in the environment. Humans around the world have daily exposure to it indoors and outdoors from multiple sources.
TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder is packaged in green and white aerosol cans with Lot codes located on the bottom of the can.
Samples of the recalled lots below have been found to contain trace levels of Benzene related to the propellant that sprays the product out of the can. Benzene is not an ingredient in any Ting products.
- Product: TING 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder, NDC: 63736-532-05, Lot Code: 0H88645, Expiration: 07/24, Package Size: 4.5 oz/128 g
- Product: TING 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder, NDC: 63736-532-05, Lot Code: 0B88345, Expiration: 02/24, Package Size: 4.5 oz/128 g
Insight has notified retailers via overnight mail to remove any remaining recalled product from shelves and follow the instructions provided in the Drug Recall Notification. The company will also offer reimbursement for consumers who have purchased TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray marked with one of the lot codes.
In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Insight Pharmaceuticals
Brand name: TING®
Product recalled: 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder
Reason for the recall: Presence of benzene
FDA Recall date: November 24, 2023
They come as -vogue house live service.
fashionlandf service…. All from hong konk
This is what they sent, then wanted me to mail it back to them at my expense of $17.00, so it was sent but of course never received.
Your order has been shipped out and on its way normally. You can enter your tracking number: AG5195377**** here:17track.net ... for tracking your order and viewing details, but please note that there is a delay in updating tracking information in this online system. And the shippers informed us that under the very strict custom inspection, which might cause the delay, could you please kindly wait for it.
2 weeks ago
I received a package in the mail addressed to me with my name and address. Upon opening it, the package was a women's diamond ring. The only return address on the package is 2800 N. Franklin Road, Indianapolis, IN.
I received a clear cheap phone case which appears to be for an iPhone 14 from 4868 Duff Dr., Cincinnati, OH. I don’t know what the scam would be, but why would someone send a postage paid and ordered item to so many people? It also states... “please contact seller directly, we are shipper, not seller space space ZR2019*****”
Last 30 days