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Wendy's, 13430 W Maple Rd, Omaha, NE 68164, United States
Total all time reports:
1
Latest report: May 26, 2020 9:34 PM
More incidents from:
Restaurant
Wendy's
Food Safety
13430, West Maple Road
Omaha
Nebraska
United States
Raw Chicken
May 26, 2020 9:34 PM
“Wifey wants to thank you for the raw chicken sandwich and upcoming bout of diarrhea. PukeCity See Less”
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1 person found this review helpful
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“Company name: Teva Pharmaceuticals
Brand name: Teva
Product recalled: Topotecan Injection 4 mg/4 mL (1 mg/mL)
Reason of the recall: Presence of particulate matter
FDA Recall date: July 01, 2021
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The administration of an injectable product that contains particulate matter may result in local irritation or swelling in response to the foreign material. If the particulate matter reaches the blood vessels it can travel to various organs and block blood vessels in the heart, lungs or brain which can cause stroke and even lead to death. While the health hazard risk could be severe if particulate matter is infused, Teva’s internal health assessment determined that the likelihood of patient exposure to impacted product is remote or unlikely.
To date, Teva has received no further complaints or reports of illness or injury.
- Carton NDC: 0703-4714. Vial NDC: 0703-4714-71. Lot# 31328962B. Exp. Date: 04/2022
Topotecan Injection, as a single agent, is indicated for the treatment of patients with metastatic ovarian cancer after disease progression on or after initial or subsequent chemotherapy and for patients with small cell lung cancer (SCLC) platinum-sensitive disease who progressed at least 60 days after initiation of first-line chemotherapy. It is also indicated for treatment of patients with Stage IV-B, recurrent, or persistent cervical cancer which is not amenable to curative treatment, in combination with cisplatin. It is packaged in 4 mg/4 mL single use vials. The affected product information is listed in the table above. Teva distributed the product nationwide to six of its Wholesale customers.
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Check the full recall details on fda.gov
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July 19, 2021 9:02 PM
“Company name: Alpha Male Plus
Brand name: Alpha Male Plus
Product recalled: Alpha Male Plus Male Enhancer fruit chew
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 19, 2021
Recall details: Tucson, AZ, Alpha Male Plus is voluntarily recalling all lots within expiry of Alpha... See More Male Plus Male Enhancer fruit chews to the consumer level. FDA analysis has found the product to be tainted with tadalafil, an ingredient known as a phosphodiesterase (PDE-5) inhibitor found in a FDA approved product for the treatment of male erectile dysfunction. The presence of tadalafil in Alpha Male Plus Male Enhancer renders the product an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Risk Statement: Consumers with underlying medical conditions who take Alpha Male Plus Male Enhancer with undeclared tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, Alpha Male Plus has not received any reports of adverse events related to this recall.
The tainted Alpha Male Plus Male Enhancer product was manufactured by Dr Manuel Mascarenas M.D. in Tucson, Arizona located at 5190 E Farness Dr Ste 104, 85712. Dr Mascarenas is the originator and manufacturer of these products for the global market. Alpha Male Plus was selected to act as the US distributor and distribute these products for the US market.
The tadalafil ingredient was never disclosed or made known to its US distributor and was only discovered through FDA laboratory analysis. Dr Manuel Mascarenas is solely responsible for the creation, formulation and proliferation of this product. Through the use of concealment, dishonest means and an unknowing 3rd party Dr Mascarenas was able to begin distributing this mislabeled and potentially harmful product to the US market.
Alpha Male Plus was marketed as a dietary supplement for male sexual enhancement and is packaged in 1strip per foil pouch within a cardboard box, UPC [8 60003 03770 6] [8 60003 74512 0].
The affected Alpha Male Plus Male Enhancer includes all lots. The product was distributed nationwide in the USA via internet directly to consumers via their website.
Company is notifying its distributors and customers by e-mail and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using or return to place of purchase/discard/contact their doctor, etc.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
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Their of money, Brookville, OH, USA
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June 29, 2021 2:00 PM
“Company name: Manna Pro Products, LLC
Brand name: Flock Party
Product recalled: Duck treats
Reason of the recall: Potential to be contaminated with Salmonella
FDA Recall date: June 29, 2021
Recall details: Company Announcement Manna Pro Products, LLC, St. Louis, Missouri, is voluntarily recalling a single lot... See More of Flock Party Quack Snacks (poultry treat) with a Best By date of 12/2023, packaged in 1.68 pound bags because it has the potential to be contaminated with Salmonella.
Manna Pro Products LLC was informed by the State of West Virginia of a positive Salmonella spp. result in a routine surveillance sample of Flock Party Quack Snacks.
Salmonella is a risk to humans from handling contaminated products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.
The bags are magenta and light blue in color and made of plastic (see images below). These products have a Best By date of 12/2023, which is printed on the bottom of the bag. This voluntary recall applies only to Flock Party Quack Snacks with Best By dates of 12/2023.
Distribution of this product has been suspended while Manna Pro continues its investigation as to the source of the contamination. This product was distributed beginning February 2, 2021 at retail stores throughout the United States.
Customers who purchased Flock Party Quack Snacks with a Best By date of 12/2023 should stop feeding the product immediately, throw the product away, and contact Manna Pro at the phone number below for a full refund. Customers with questions or concerns should contact Manna Pro at (800) 690-9908 ext. 2, Monday through Friday from 8:00 AM to 4:00 PM Central time. Members of the media can should refer their inquiries to Noah Messel of O’Malley Hansen at (314) 656-8302 or Noah.Messel@omalleyhansen.com.
Check the full recall details on fda.gov
Source: FDA See Less”
Diagnosis: Salmonella
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Augusta, GA, USA
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