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4061 Indian Creek Parkway, Overland Park, Kansas, United States

Updated:

A

Covid-19 OSHA Complaint, Saint Luke's Primary Care Mission Farms, 4061 Indian Creek Parkway, OVERLAND PARK, KS, 66207, USA

2 years ago

employees are beings asked to collect COVID-19 tests without training; Covid-19 positive patients are not being kept quarantined from other patients.


Source: Osha.gov | Receipt Date: 2021-12-30

#coronaviruscovid19 #osha #4061indiancreekparkway #overlandpark #kansas #us

378

Recent Interesting Reports

Aruba Aloe Hand Sanitizer Gel and Alcoholada Gel - recalled because they contain Methanol, USA

3 weeks ago •source www.fda.gov

Recall notice

Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel to the consumer level. The products have been found to contain alcohol denatured with methanol. Products were distributed between 5/1/2021 and 10/27/2023 and sold in … See More
the US online only via the Aruba Aloe Balm N.V. website. To date, Aruba Aloe Balm N.V. has not received any reports of adverse events related to these products.

Aruba Aloe Hand Sanitizer Gel is used as a sanitizer to help reduce bacteria that potentially can cause disease and is packaged in 12 fl oz (355 mL) dark green plastic bottles with white label reading in part “ARUBA ALOE Hand Sanitizer GEL 80% Alcohol Made in Aruba World’s Finest Aloe”, with barcode 0 82252 03300 5.

Aruba Aloe Alcoholada Gel is used for temporary relief of pain and itching associated with minor burns, sunburn, insect bites, or minor skin irritations and is packaged in two sizes: 2.2 fl oz (65 mL) plastic bottles with barcode 0 82252 34030 1 and 8.5 fl oz (251 mL) plastic bottles with barcode 0 82252 03120 9. The plastic bottles are transparent with a label reading in part “Alcoholada Gel Pain Relieving Gel 0.5% Lidocaine Hydrochloride”.

The affected Aruba Aloe Hand Sanitizer GEL product lots (filled in 12, 2.2, and 8.5 fl. oz bottles bottles) can be viewed in the link below.

Aruba Aloe Balm N.V. has notified all customers that bought these products by email and has offered a discount coupon for a next purchase. Consumers that have products which are being recalled should stop using and discard the product.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache blurred vision, coma, seizures, permanent blindness, permanent damage to the central 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.

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: Aruba Aloe Balm N.V.
Brand name: Aruba Aloe
Product recalled: Hand Sanitizer Gel and Alcoholada Gel
Reason of the recall: Product contains methanol
FDA Recall date: April 05, 2024

Source: www.fda.gov
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#recall #us

Aruba Aloe Hand Sanitizer Gel and Alcoholada Gel - recalled because they contain Methanol photo #1
303
N

Scam Alert, Portland, OR, USA

2 weeks ago •reported by user-ndcmr139

I received a package from Shipping Center, 5572 Silver Hill Rd, Bryan TX that I never ordered. USPS Tracking # 9200 1903 1714 8120 0282 144****. USPS should be able to determine who originated the tracking code. I was recently scammed by a fake website that resulted … See More
in a charge by WWW .WEBSHOP-SRL. COM MILANO IT, which I have disputed
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#scam #onlineshopping #onlinescam #delivery #uspostalservice #portland #oregon #us

Scam Alert photo #1
712

Tejocote Dietary Supplements - recalled because it contains toxic yellow oleander, USA

2 weeks ago •source www.fda.gov

Recall notice

Global Mix, Inc. of New York, is recalling tejocote products to include the following brands: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra. The recalled products are labeled as tejocote root but are toxic yellow oleander. The recalled products were distributed in the following states: AL, AK, … See More
CA, CO, CT, DE, FL, GA, HI, ID, IL, IA, IN, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NM, NC, NY, NJ, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI, and WY through website. The recalled products were also sold via the below websites via courier direct delivery and mail order. Etsy, amazon, eva-nutrition, tejocotemexican, niwali, scienceofalpha. The recalling firm has not received any reported of illness.

Recalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.

Product Name: Eva Nutrition MexicanTejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Science of Alpha Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: NWL Nutra Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Niwali Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025

Per the safety alert update on 3/12/24, "The FDA continues to receive adverse event reports related to the products identified in this Safety Alert."

The recall was the result of a routine sampling program by the company which revealed that the finished products contained the yellow oleander. The company has ceased the production and distribution of the product as the company continues their investigation as to what caused the problem. Further the company is conducting comprehensive quality control and monitoring process.

Customers who have purchased these products should stop using them immediately and return them to the point of purchase for a full refund.

Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.

Company name: Global Mix, Inc.
Brand name: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra
Product recalled: Tejocote Dietary Supplements
Reason of the recall: Product contains toxic yellow oleander.
FDA Recall date: April 10, 2024

Source: www.fda.gov
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#recall #us

Tejocote Dietary Supplements - recalled because it contains toxic yellow oleander photo #1
303
B

Cynthia D. Blanchard and Copper Tree Management Price Tower, Bartlesville, Oklahoma, USA

3 weeks ago •reported by user-bxhk3293

Cynthia Blanchard has told lie after lie to literally steal money via wire fraud in a series of crypto currency investments and then real estate transactions. Cynthia Blanchard took our money via wire transfer and more money via crypto currencies to give us bogus fraudulent stock, fake … See More
crypto currency, fake crypto backed by gold called AGLD for AnthemGold. com a missing website. Her other businesses AnthemVault. com is out of business and even HeraSoft. com she claimed had contracts with foreign governments and the State of California and the Department of Energy is also gone from the internet and out of business. She now claims they are selling the building that was supposed to be the corporate headquarters that was purchased with our investment capital and now she is running the PriceTower in Bartlesville Oklahoma, a tall building built by Frank Lloyd Wright that she says she bought for $10 and if we want our money we need invest more in the PriceTower. Enough with the fraud, dishonesty, misrepresentations. Give us our money back and go directly to jail you LIAR! Cynthia D. Blanchard is a LIAR and a fraud, she belongs in Prison!
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#scam #bartlesville #oklahoma #us

Cynthia D. Blanchard and Copper Tree Management Price Tower photo #1
17

Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil, USA

4 days ago •source www.fda.gov

Recall notice

STOP CLOPEZ CORP is voluntarily recalling one lot of Schwinnng capsules to the consumer level. FDA analysis has found the Schwinnng products to contain Nortadalafil. Nortadalafil is an active drug ingredient known for the treatment of male erectile dysfunction. The presence of Nortadalafil in Schwinnng capsules makes … See More
it an unapproved new drug for which the safety and efficacy have not been established and, therefore subject to recall. The product was distributed Worldwide via Amazon at www.amazon.com. To date, no adverse events have been reported.

The Schwinnng products contain Nortadalafil, which may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.

This product is marketed as a dietary supplement for male sexual enhancement and is packaged and coded as follows:

SCHWINNNG Lot 2108 EXP 10/2024

STOP CLOPEZ CORP is notifying its customers by this press announcement of this recall release and is arranging for a return of all recalled products. Consumers that have a Schwinnng product that is being recalled should stop using and destroy / return if desired to STOP CLOPEZ CORP. Schwinnng products must include the blister pack foil (with any pills remaining) containing all lot codes and receipt of proof of purchase, and your return address.

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.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Link to FDA Advisory

If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.

Company name: STOP CLOPEZ CORP
Brand name: Schwinnng
Product recalled: Herbal Dietary Supplement
Reason of the recall: Product is tainted with Nortadalafil
FDA Recall date: April 23, 2024

Source: www.fda.gov
See Less

#recall #drugs #us

Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil photo #1
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