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Nevada, United States
Updated: April 7, 2021 12:00 PM
Covid-19 OSHA Complaint, The Apothecary Shoppe - Las Vegas Dispensary, 4240 West Flamingo Road, LAS VEGAS, NV, 89103, USA
The Apothecary Shoppe - Las Vegas Dispensary, 4240 West Flamingo Road, LAS VEGAS, NV, 89103, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to employees completing the required self-quarantine. There is concern that employees were exposed to COVID-19 positive employees and were not required to self-quarantine. HAZARD LOCATION: Throughout. 3/12/2021 JH
Alleg... See Moreed Hazards: 1,
Source: Osha.gov | Receipt Date: 2021-03-12 See Less”
Helpful
Covid-19 OSHA Complaint, Zenith American Solutions, Inc., 9121 West Russell Road, LAS VEGAS, NV, 89148, USA
Zenith American Solutions, Inc., 9121 West Russell Road, LAS VEGAS, NV, 89148, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to employees staying home while showing symptoms related to COVID-19. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to employees' quarantine period after testing positive for COVID-19. T... See Morehe employees and owner returned to work after testing positive for COVID-19. Hazard location: Suite 208 3/3/2021 EH
Alleged Hazards: 2, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2021-02-26 See Less”
Helpful
Covid-19 OSHA Complaint, Amazon DLV1, 3165 West Sunset Road Suite 120, LAS VEGAS, NV, 89118, USA
Amazon DLV1, 3165 West Sunset Road Suite 120, LAS VEGAS, NV, 89118, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to social distancing between employees. Employer requires employees to meet in groups of 6 or more to pick up merchandise that is prepared for distribution. At that location, there is usually driver crowding around the t... See Moreotes. HAZARD LOCATION: 1. Inside warehouse where drivers are assigned pick-ups. 2/24/2021 JH
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2021-02-24 See Less”
Helpful
Covid-19 OSHA Complaint, Costco Wholesale #685, 801 South Pavilion Center Drive, LAS VEGAS, NV, 89144, USA
Costco Wholesale #685, 801 South Pavilion Center Drive, LAS VEGAS, NV, 89144, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to social distancing between employees. A supervisor brought multiple breakroom tables and employees together during a meal break, with less than 6 feet of separation between the approximately 5 seated employees. The sup... See Moreervisor then announced that the violation of social distancing was allowed due to her allowing it. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to persons/patrons wearing face coverings while in the Employer's establishment. Management is not speaking to or reminding customers to wear their face covers, even when walking directly past customers who are not wearing face covers. Hazard Location: 1. Breakroom area. 2. Throughout the site. 2/22/2021 JB
Alleged Hazards: 2, Employees Exposed: 2
Source: Osha.gov | Receipt Date: 2021-02-22 See Less”
Helpful
Covid-19 OSHA Complaint, Worldwide Flight Services, McCarran International Airport, LAS VEGAS, NV, 89144, USA
Worldwide Flight Services, McCarran International Airport, LAS VEGAS, NV, 89144, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to social distancing between employees and the public. Employees are not socially distanced from boarding passengers. The employer is advising employees that they are in compliance due to face cover use, which allegedly... See Moreallows social distancing to not be maintained. 2. The employer is advising employees to not advise other employees if they tested positive for COVID-19. 3. The employer is not complying with the Governor's COVID-19 mandate in regard to requiring employee self-quarantine. The employer is not quarantining employees who stood/worked directly next to a COVID-19 positive employee. HAZARD LOCATION: 1. Allegiant ticket counter and gates in Terminal 1, departure. 2. Throughout. 2/4/2021 JH
Alleged Hazards: 3,
Source: Osha.gov | Receipt Date: 2021-02-04 See Less”
Helpful
Covid-19 OSHA Complaint, Romano's Macaroni Grill, 2001 North Rainbow Boulevard, LAS VEGAS, NV, 89108, USA
Romano's Macaroni Grill, 2001 North Rainbow Boulevard, LAS VEGAS, NV, 89108, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to following CDC guideline for employees who have had close contact (within 6 feet for 15 minutes or longer) with an individual who tested positive for COVID-19. Employees are not informed they may have had close contact... See Morewith individuals who tested positive for COVID-19. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to following CDC guidelines for employees who test positive for COVID-19. Employees continue to work after testing positive for COVID-19. 3. The employer is not complying with the Governor's COVID-19 mandate in regard to requiring employees to stay home if symptomatic. The employer does not encourage employees to stay home if symptomatic. Hazard Location: In the restaurant area 01/26/2021 EM
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-01-26 See Less”
Helpful
Covid-19 OSHA Complaint, Denny's, 1822 South Las Vegas Boulevard, LAS VEGAS, NV, 89104, USA
Denny's, 1822 South Las Vegas Boulevard, LAS VEGAS, NV, 89104, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to employees wearing face coverings. Employees are not wearing face masks or are wearing incorrectly below the chin while working in the establishment. 2. The employer is not complying with the Governor's COVID-19 mandat... See Moree in regard to social distancing between employees and the public. Employees are required to come in close proximity to the customers. 3.The employer is not complying with the Governor's COVID-19 mandate in regard to maintaining 25% occupancy limit. 4. The employer is not complying with the Governor's COVID-19 mandate in regard to employees testing positive at the workplace. Employees have tested positive for COVID-19 and the employer has not performed trace contact to ensure employees who were exposed quarantine for 10 days. Hazard Location: Throughout 1/22/2021 DJ
Alleged Hazards: 4, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2021-01-22 See Less”
Helpful
Covid-19 OSHA Complaint, Mandalay Bay Resort and Casino, 3950 South Las Vegas Blvd, LAS VEGAS, NV, 89119, USA
Mandalay Bay Resort and Casino, 3950 South Las Vegas Blvd, LAS VEGAS, NV, 89119, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to providing disinfectant to wipe down high touch surfaces on the casino floor. The employees are not being provided with disinfectant for cleaning purposes. The Director provides the EVS staff with water in the spray bo... See Morettles which are then used for wiping down high touch surfaces on the casino floor. The employer is potentially exposing employees and the public to contracting the COVID-19 virus. Hazard Location: Casino floor 1/15/2021 JB
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2021-01-15 See Less”
Helpful
Covid-19 OSHA Complaint, Mastercorp, Inc., 75 East Harmon Avenue, LAS VEGAS, NV, 89109, USA
Mastercorp, Inc., 75 East Harmon Avenue, LAS VEGAS, NV, 89109, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to employees quarantining after they return from out of the country. An employee of MasterCorp inc. returned from Cuba on December 22, 2020, and following news of that return, the controlling employer Marriott instructed... See Morethe employee to leave the property. The employee was originally told to return to work January 4, 2021 by the employer. However, on December 30,2020, the employee was contacted by management and other employer representatives and directed to work at a different property. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to employees quarantining after they return from out of the country. A manager returned from Mexico on September 1, 2020. On September 5, 2020, the manager returned to work in lieu of following the quarantine guidelines. 3. On November 24, 2020, a house keeper was directly exposed by a positive COVID-19 family member. When this information was communicated to MasterCorp Inc. management, they informed the housekeeper to return to work. On November 27, 2020, the controlling employer Marriott assessed the employee and directed the employee to leave the property in accordance with current COVID-19 guidelines. 4. Employees are concerned that the personal protective equipment provided for the purposes of sanitizing high-touch surfaces is inadequate and no additional protective equipment is provided. Hazard Location: Housekeeping Area, guest rooms. 12/30/2020 bm
Alleged Hazards: 4,
Source: Osha.gov | Receipt Date: 2020-12-30 See Less”
Helpful
Covid-19 OSHA Complaint, Real Sports, Inc., 3520 East Tropicana Avenue, LAS VEGAS, NV, 89121, USA
Real Sports, Inc., 3520 East Tropicana Avenue, LAS VEGAS, NV, 89121, USA
April 7, 2021 12:00 PM
“1. The employer is not complying with the Governor's COVID-19 mandate in regard to employees wearing face coverings. Limited face coverings are used within work areas. 2. The employer is not complying with the Governor's COVID-19 mandate in regard to maintaining a minimum 6-feet of separation betwee... See Moren workspaces. 3. The employer is not complying with the Governor's COVID-19 mandate in regard to sanitizing high-touch surfaces after each use. Third party cleaning services are only being done once a week. Hazard Location: Throughout the business 12/21/2020 FL
Alleged Hazards: 3,
Source: Osha.gov | Receipt Date: 2020-12-21 See Less”
Helpful
Recent Interesting Reports
April 6, 2021 9:13 PM
“Got my first shot yesterday afternoon at Walgreens. Felt fine most of the evening. Woke up at 1am and my left arm (I had the shot in my left arm) was numb along with the left side of my face. I started to panic thinking great it’s a stroke but I read about temporary Bell’s palsy and calmed down and... See Morewent to sleep. Woke up at 8:30. My arm was very sore which got worse as the day went on, I was very fatigued and had a low fever which Tylenol got rid of. Aches and pains came and went all day. My top lip on my left side of my mouth is still numb and parts of my face feels numb still but I look fine and feel fine otherwise. 30 hours later i would say the worst is the arm pain, I can’t really use my arm. I suggest getting it in your non dominant arm/hand which was suggested to me. Overall the numbness was scary but I think the vaccine is worth it. See Less”
Helpful
1 person found this review helpful
April 6, 2021 5:00 PM
“Company name: Yolo Studio
Brand name: PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: April 06, 2021
Recall details: Company Announcement Cli... See Moreffside Park, NJ, Yolo Studio is voluntarily recalling all lots of PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 to the consumer level. FDA analysis has found the product to contain undeclared tadalafil. Tadalafil is ingredient known as a phosphodiesterase (PDE-5) inhibitor found in FDA approved products for the treatment of male erectile dysfunction. The presence of tadalafil in PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 makes these unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall.
Consumers with underlying medical issues who take PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 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, Yolo Studio has not received any reports of adverse events related to this recall. These tainted products are marketed as dietary supplements for male sexual enhancement and are packaged in cardboard blisters containing one pill per card.
The affected lot numbers of PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 include all lots. PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 were distributed via internet and fulfilled by amazon at www.amazon.com nationwide in the USA. On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.
Yolo Studio is notifying its customers by this press announcement and via e-mail of this recall. Consumers that have PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500 which are being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Yolo Studio by phone at (201) 233-3521 Monday through Friday from 9am to 5pm eastern time zone or e-mail yolostudiodamazon@gmail.com.
Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to taking or using these drug products. 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.
- Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
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”
Helpful
Dream Bone Treats, Scott, AR, USA, Scott, AR, USA
Scott, AR, USA
March 24, 2021 9:25 AM
“My yar old cocker spaniel just had a seizure after giving him 2 dream bone peanut butter treats! Poor lil guy ate 2 of these shitty made in China peanut butter treats! Next thing I see is him convulsing on the floor uncontrollably! Very sad to have to watch! His half sister has been having them for... See More2 years , but it’s gotta be coming from this treat. Do not ever feed your dogs these. I am devasted to now have 2 dogs that have has seizures due to this. See Less”
Helpful
2 people found this review helpful
March 24, 2021 4:00 PM
“Company name: Alembic Pharmaceuticals, Inc.
Brand name: Alembic
Product recalled: Telmisartan Tablets, USP, 20 mg
Reason of the recall: Incorrect Product Strength on Label
FDA Recall date: March 24, 2021
Recall details: Bridgewater, NJ, Alembic Pharmaceuticals, Inc is voluntarily recalling on... See Moree lot of Telmisartan Tablets, USP, 20 mg, packaged in 30-count bottles, Lot No. 1905005661 to the consumer level. The product is being recalled due to a market complaint received which stated that one bottle labelled as 30-count Telmisartan Tablets, USP, 20 mg incorrectly contained 30 tablets of Telmisartan Tablets, USP, 40mg.
Risk Statement: Patients who could be on a doubled dose of telmisartan for a prolonged period of time, could experience low blood pressure, worsening of kidney function, or an elevation of potassium which can be life-threatening. To date, Alembic Pharmaceuticals Limited has not received any reports of adverse events related to this recall. The product is used for the treatment of hypertension i.e. to lower blood pressure and is packaged in a bottle of 30 tablets having NDC Number 62332-087-30.
The affected lot of Telmisartan Tablets, USP, 20 mg is the lot number 1905005661 and the lot expires in March 2022. The wrong product can be identified by checking the shape and embossing details on the tablets i.e. Telmisartan Tablets, USP, 20 mg bottles may incorrectly contain oval shaped White to off-white tablets debossed with L203 on one side instead of correct product i.e. round shaped White to off-white tablets debossed with L 202 on one side. Telmisartan Tablets, USP, 20mg, Lot No. 1905005661 was distributed Nationwide in the USA to wholesalers, retailers, and pharmacies.
Alembic Pharmaceuticals Limited is notifying its distributors and retailers through letter and is arranging for return of the recalled lot. Consumers that may have Telmisartan Tablets, USP, 20 mg which is being recalled should not discontinue use until speaking with their pharmacist or healthcare professional for a replacement before returning to place of purchase. Consumers with questions regarding this recall can contact Alembic Pharmaceuticals Inc by phone at +1 908-552-5839 (9:00 am – 5:00 pm, EDT, Monday through Friday) or email address david.cobb@alembicusa.com.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
1 person found this review helpful
Johnson&Johnson vaccine, Kansas City, KS, USA
Kansas City, KS, USA
April 9, 2021 3:15 PM
“I got the j&j vac at 1:00pm its been 1 hour so far only a slight tingling on vaccination spot other than that nothing big hoping for the best See Less”
Helpful
1 person found this review helpful
April 4, 2021 6:56 PM
“The CDC announced that they are currently investigating a multistate outbreak of Salmonella infections where 19 people have been reported sick from 8 states (CA, KY, MS, NH, OK, OR, TN, WA). Eight people of the total have required hospitalization but no deaths have been reported to date.
Accordin... See Moreg to the outbreak notice, there are reports of wild songbirds, such as pine siskins (small, streaked, yellow-tinged songbirds in the finch family) sick with the same strain of Salmonella that is making people sick in this outbreak. Salmonella germs can spread between species of birds, to pets, and to people.
You can get sick when you touch your mouth with unwashed hands after touching wild birds, bird feeders or bird baths, or your pets that have contact with wild birds.
CDC advises to:
- Clean and disinfect your bird feeder and bird bath weekly or when they are visibly dirty.
- Do not touch or hand-feed wild birds with your bare hands.
- Always wash your hands with soap and water
- Call your healthcare provider right away if you have any of these severe Salmonella symptoms
Most people infected with Salmonella develop diarrhea, fever, and stomach cramps 6 hours to 6 days after being exposed to the bacteria and the illness usually lasts 4 to 7 days, and many recover without treatment.
Check the CDC website for the full investigation details cdc.gov
Source: CDC See Less”
Doctor Visit: Yes
Diagnosis: Salmonella
Helpful
1 person found this review helpful
March 30, 2021 10:00 AM
“Company name: Bit & Bet LLC
Brand name: Thumbs Up 7
Product recalled: Blue 69K Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 30, 2021
Recall details: Bit & Bet LLC is voluntarily recalling all lots of Thumbs Up 7... See MoreBlue 69K capsules to consumer level. FDA analysis has found the product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction.
The presence of sildenafil and tadalafil in Thumbs Up 7 Blue 69K capsules make them unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall. Consumers with underlying medical issues who take Thumbs Up 7 Blue 69K capsules with undeclared sildenafil and 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, Bit & Bet has not received any reports of adverse events related to this recall. To date, Bit & Bet has not received any reports of adverse events related to this recall This tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in blister foil sheets in a box labeled with UPC 6 17135 89467 3. Each box contains 10 capsules. The affected lot numbers of Thumbs Up 7 Blue 69K includes all lots. Thumbs Up 7 Blue 69K was distributed via internet and fulfilled by amazon at www.amazon.com nationwide in the USA.
On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, e Bay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms. Bit & Bet LLC is notifying its customers by this press announcement and via email of this recall. Consumers that have Thumbs up 7 Blue 69K, which is being recalled should stop using and descard them.
Consumers with questions regarding this recall can contact Bit & Bet LLC by phone at (201) 208-2836 Monday to Friday from 9AM to 5PM or e-mail thumbsup7blue@gmail.com. For more information, please visit www.thumbsup7blue.com. Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to takin 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. 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”
Helpful
March 29, 2021 8:00 PM
“Company name: Antoto-K
Brand name: Thumbs Up 7
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 29, 2021
Recall details: Manassas, VA, Antoto-K is voluntarily recalling all lots of Thumbs Up 7 Red 7... See More0K, 10 capsules to consumer level. FDA analysis has found the product to contain undeclared Sildenafil and Tadalafil. Sildenafil and Tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction.
The presence of Sildenafil and Tadalafil in Thumbs Up 7 Red 70K, 10 capsules makes them unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall. Consumers with underlying medical issues who take Thumbs Up 7 Red 70K, 10 capsules with undeclared Sildenafil and 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, Antoto-K has not received any reports of adverse events related to this recall. This tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in foil sheet and a box containing 10 capsules. The affected lot numbers of Thumbs Up 7 Red 70K includes all lots. Thumbs Up 7 Red 70K was distributed via internet and fulfilled by amazon at www.amazon.com nationwide in the USA.
On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms. Antoto-K is notifying its customers by this press announcement and via e-mail of this recall. Consumers that have Thumbs Up 7 Red 70K which is being recalled should stop using and destroy them.
Consumers with questions regarding this recall can contact Antoto-K by email at ngtbtr.k17@gmail.com. Consumers should contact their physicians 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. 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”
Helpful
1 person found this review helpful
I am reporting Pfizer vaccine, Lecompte, LA 71346, USA
Symptoms: Other
Headache
Lecompte, LA 71346, USA
March 22, 2021 7:48 PM
“In February I received my 1st dose of Pfizer vaccine and I did get a headache.. yet it was the second dose on March 3 that made me go to the doctor and found that that vaccine has cause me to have high high blood pressure! My numbers doubled and I have not recovered. Now on high blood pressure me... See Moreds. The doctor says I have fluid built up around my heart and palpitations that are driving me to unhappy days.
Letting you know. . See Less”
Helpful
5 people found this review helpful
March 31, 2021 12:02 PM
“Company name: Nuri Trading LLC
Brand name: Thumbs Up 7, Shogun-X, 69MODE
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil, Tadalafil, Vardenafil
FDA Recall date: March 31, 2021
Recall details: Nuri Trading is voluntarily recalling all... See Morelots within expiry of Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, and 69MODE Blue 69 capsules to the consumer level. FDA analyses have found these products to contain undeclared tadalafil, sildenafil, and/or vardenafil. Sildenafil,tadalafil, and vardenafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction.
The presence of sildenafil, tadalafil, and/ or vardenafil in Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, and 69MODE Blue 69 capsules make them unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall.
Consumers with underlying medical issues who take Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69 capsules with undeclared sildenafil,tadalafil, and/or vardenafil 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, Nuri Trading has not received any reports of adverse events related to this recall. These tainted products are marketed as dietary supplements for male sexual enhancement and are packaged in blister foil sheets in a box. Each box contains 10 capsules. These products were distributed via internet and fulfilled by amazon at www.amazon.com nationwide in the USA. On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.
Nuri Trading LLC is notifying its customers by this press announcement and via email of this recall. Consumers that have Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69, which are being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Nuri Trading by phone at (201) 380-1046 Monday to Friday from 9AM to 5PM eastern time or e-mail nuritrading17@gmail.com. For more information, please visit www.nuritradingusa.com.
Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to takin 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. 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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