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Applebee's Grill + Bar, 5605 2nd Ave, Kearney, NE 68847, USA
Latest report: July 5, 2020 12:00 PM
RT
Employee test positive for Covid-19
1 year ago
An Applebee's worker at the 5605 Second Ave. location contracted COVID-19. The team member worked on June 21/
Source: kearneyhub.com See Less
12
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About 6 minutes after taking second pfizer dose, I began to sweat, blood pressure dropped, nausea set in and almost lost consciousness a couple of times. A nurse and a doctor stayed with me and offered some water. That didn't help ad after about an hour, I... See More was taken by ambulance to emergency room and treated with fluids and anti-nausea feeds. About 5-6 hours later I began to feel better and went home. | Symptoms: Nausea See Less
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Recent Interesting Reports
I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT See Less
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Nutrisure Ltd is recalling Naturya Hemp Protein Powder because it contains gluten, which is not mentioned on the label. This means the product is a possible health risk for anyone with an allergy or intolerance to gluten. This batch was only sold in Sainsbury’s stores.
Naturya Hemp... See More Protein Powder (100g)
Pack size: 100g
Batch code: W02135
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Allergens: Gluten
If you have bought the above product and have an allergy or intolerance to gluten, do not eat it. Instead, return it to the store from where it was bought for a full refund.
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Product recalled: Naturya Hemp Protein Powder
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Check the full recall details on food.gov.uk
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International Golden Foods, Inc (IGF) of Bensenville, IL is voluntarily recalling certain lot codes of the Al kanater brand tahini because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people... See More and others with weakened immune system. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The product was distributed nationwide and is sold in 16 Oz. jars. The jars are labelled “Al kanater Tahini.” Lot codes are printed on the jar. Product code, description, lot code, and UPC information are noted below.
Product Code: AT1LB
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No illnesses have been reported to-date in connection with the Al Kanater Brand Tahini.
This problem was revealed as a result of a random sampling by the Michigan Department of Agriculture.
Consumers who have purchased Al kanater Tahini with these lot codes should discontinue use and return it to the store of purchase for a full refund. Retailers that may have further distributed the recalled lot codes should share this notice with their customers.
Company name: International Golden Foods, Inc.
Brand name: Al Kanater
Product recalled: Tahini
Reason of the recall: Salmonella
FDA Recall date: November 30, 2021
Check the full recall details on fda.gov
Source: FDA See Less
101
NJ post office is a ‘black hole’, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
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On 9-24-21 I valued package was returned using Pitney Bowes shipping label provided by the merchant (American Mint). It was dropped off at the USPS store in Daytona Beach, picked up by Daytona Beach Post Office on 9-28-21 and retrieved from that Post office by Newgistics (Pitney... See More Bowes) on 9-30-21. On 10-4-21 it arrived and was dispatched from sorting at the Monroe Township, Middlesex County, New Jersey Post Office. Since then it is missing, in a black hole, unable to be found. This is a shame since this is a product scammed to my mother (senior of 86) who followed every step to have her $149.99 from American Mint and now can not receive her money back since the company has not received the product back. Please address this issue to return what is rightfully my mother's. This is a shame.
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American Screening LLC of Shreveport, Louisiana is voluntarily recalling 153,336 units of Hand Sanitizer, containing 70% ethyl alcohol gel to the consumer level. The hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption.
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The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in an eight-ounce bottle. The affected hand sanitizer lots include the following expiration dates of 5/21/2022 and 05/24/2022 for black-capped bottles and no lot numbers or expiration dates for clear capped bottles. The product can be identified by its shape (small water bottle), with a black flip top cap or clear cap with blue pouring spout with the weight of measure of eight (8) ounces/237mL, UPC 8 4005051579 2.
The Hand Sanitizer was sold to customers & distributors Nationwide via the internet at americanscreeningcorp.com and/or in-house sales.
Consumers & distributors that have this hand sanitizer which is being recalled should stop distribution/use and return to place of purchase or discard. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to ingesting the hand sanitizer packaged in the 8 oz. water bottle style.
Company name: American Screening LLC
Brand name: American Screening
Product recalled: Hand Sanitizer
Reason of the recall: Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption
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Check the full recall details on fda.gov
Source: FDA See Less
102
Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products.
Risk Statement: Benzene is... See More classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.
To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See the link below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically the ones listed in the link below.
The products were distributed nationwide in the United States through various retailers. Consumers, distributors, and retailers that have product which is being recalled should stop using or selling these specific Odor-Eaters® spray products and dispose of them appropriately.
Company name: Odor-Eaters®, owned by Blistex Inc.
Brand name: Odor-Eaters®
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Reason of the recall: Due to the presence of benzene
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Check the full recall details on fda.gov
Source: FDA See Less
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On April 6, I ordered a saw for wood and I never received it! See Less
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Teterboro, NJ USPS, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
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Package was supposed to be delivered November 6, 2021.
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Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... See More no illnesses reported to date.
During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.
The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.
The full list of affected products is on the link below.
Lot numbers and expiration dates are found on the bottom of each container.
Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.
Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements
Check the full recall details on the FDA website: fda.gov
Source: FDA See Less
101
DreamBone Twist Sticks are making my dogs vomiT - from Chewy.com., Hickory Valley, TN, USA
2 weeks ago
DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.
I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so... See More far today and STILL pieces of DreamBone Twist Sticks See Less
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