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Alameda, California, United States

Updated: April 7, 2021 12:00 PM

Covid-19 OSHA Complaint, Cafe Jolie, 1500 Webster Street, ALAMEDA, CA, 94501, USA

Cafe Jolie, 1500 Webster Street, ALAMEDA, CA, 94501, USA

April 7, 2021 12:00 PM

“1. The employer failed to implement cleaning and disinfection of areas, material, and equipment used by two COVID-19 cases during the high-risk exposure period. T8 CCR 3205(c)(8)(C) 2. The employer did not investigate two COVID-19 cases in the workplace and determine which employees had COVID-19 exp... See Moreosure, nor did the employer give notice of the potential exposure, within one business day, to all employees who may have had COVID-19 exposure. T8 CCR 3205(c)(3)B) 3. The employer did not exclude employees who had COVID-19 exposure from the workplace for 10 days after the last known COVID-19 exposure to a COVID-19 case. T8 CCR 3205(c)(10)(B)

Alleged Hazards: 3, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-02-02
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Peet's Coffee, 1365 Park Street, ALAMEDA, CA, 94501, USA

Peet's Coffee, 1365 Park Street, ALAMEDA, CA, 94501, USA

April 7, 2021 12:00 PM

“The employer failed to disinfect surfaces after twelve employees were excluded from the workplace due to COVID-19 infections. T8 CCR 3205(c)(8)(C)

Alleged Hazards: 1, Employees Exposed: 12
Source: Osha.gov | Receipt Date: 2021-01-26 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Alameda Municipal Power, 2000 Grand Street, ALAMEDA, CA, 94501, USA

Alameda Municipal Power, 2000 Grand Street, ALAMEDA, CA, 94501, USA

April 1, 2021 12:00 PM

“1. The employer failed to investigate a COVID-19 case in the workplace on or about February 1, 2021. An employee who did have close contact with the COVID-19 case was not informed by the employer and was not excluded from the workplace for at least 10 days. T8 CCR 3205(c)(3)(B) 2. The employer faile... See Mored to clean and disinfect the areas, material, and equipment used by a COVID-19 case during the high-risk exposure period. T8 CCR 3205(c)(8)(C) 3. The employer failed to ensure that employees wear face coverings over the nose and mouth when indoors. T8 CCR 3205(c)(7)(A) 4. The employer failed to give notice of potential COVID-19 exposure within one business day to all employees who may have had COVID-19 exposure and their authorized representatives. T8 CCR 3205(c)(3)(B)3. 5. The employer failed to ensure that employees are separated from other persons by at least six feet. Employees in the break room sit directly across from each other and are seated back to back when facing the table. T8 CCR 3205(c)(6)(A)

Alleged Hazards: 5, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-02-10
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Reported By SafelyHQ.com User
Vaccine Side Effects Special summary

Covid-19 OSHA Complaint, Oltmans Construction Company, 1410 Harbor Bay Parkway, ALAMEDA, CA, 94502, USA

Oltmans Construction Company, 1410 Harbor Bay Parkway, ALAMEDA, CA, 94502, USA

March 24, 2021 12:00 PM

“1. The employer failed to develop and implement a process for screening employees for and responding to employees with COVID-19 symptoms. The employer may ask employees to evaluate their own symptoms before reporting to work. If the employer conducts screening at the workplace, the employer shall en... See Moresure that face coverings are used during screening by both screeners and employees and, if temperatures are measured, that non-contact thermometers are used. T8 CCR 3205(c)(2)(B) 2. The employer failed to ensure that employees were separated from other persons by at least six feet, except where an employer can demonstrate that six feet of separation is not possible, and except for momentary exposure while persons are in movement. T8 CCR 3205(c)(6)(A) 3. The employer failed to ensure that face coverings are worn by employees over the nose and mouth when indoors, when outdoors and less than six feet away from another person, and where required by orders from the CDPH or local health department. T8 CCR 3205(c)(7)(A) 4. The employer failed to require the use of seatbelts. Employees are driving equipment/vehicles without seatbelts. T8 CCR 1597(h)

Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-22
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walgreens, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

Walgreens, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

March 24, 2021 12:00 PM

“1. T8 CCR 3205(c)(2)(B) The employer failed to ensure that employees conduct effective screening prior to beginning their shift work. 2. T8 CCR 3205(c)(8)(C) The employer failed to disinfect surfaces adequately after an employee tested positive.

Alleged Hazards: 2, Employees Exposed: 15
Source: O... See Moresha.gov | Receipt Date: 2021-01-15 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walgreens, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

Walgreens, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

March 24, 2021 12:00 PM

“1. The employer failed to send home employees who are showing signs and symptoms of COVID. An employee took a test on 01/08/21 and continued to work through 01/12/21 while coughing. Employee was sent home once test results were confirmed on 01/12/21. T8 CCR 3205( c)(2)(B) 2. The employer failed to e... See Morenforce that employees wear face masks at all times. The store manager would not wear his facemask in the office and break areas, which is shared with other employees. The Store manager was also coughing during this time. T8 CCR 3205(c )(7)(A) 3. The employer failed to sanitize the common touch areas where an employee who tested positive for COVID worked on 01/12/21. T8 CCR 3205(c )(8)(C )

Alleged Hazards: 3, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-01-13
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walgreens, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

Walgreens, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

March 24, 2021 12:00 PM

“1. The employer did not develop and implement an effective process of screening employees for and responding to employees with COVID-19 symptoms. The thermometers used to take employee temperatures are defective and display the exact same temperature for all employees. T8 CCR 3205(c)(2)(B) 2. The em... See Moreployer did not clean and disinfect the areas, materials, and equipment being used by a COVID-19 case during the high-risk exposure period. T8 CCR 3205(c)(8)(C) 3. The employer did not ensure that a COVID-19 case was excluded from the workplace until the return to work requirements of subsection (c)(11) were met. T8 CCR 3205(c)(10)(B) 4. The employer did not determine who may have had COVID-19 exposure to the employee who returned to work before the requirements of subsection (c)(11) were met. T8 CCR 3205(c)(3)(B) 5. The employer failed to ensure that employees, who are confirmed COVID-19 cases, do not return to work for at least 10 days since their symptoms first appeared or for a minimum of 10 days since the date of specimen collection of their first positive COVID-19 test. T8 CCR 3205(c)(11)

Alleged Hazards: 5, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-01-19
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Donut Petit, 711 Santa Clara Avenue, ALAMEDA, CA, 94501, USA

Donut Petit, 711 Santa Clara Avenue, ALAMEDA, CA, 94501, USA

March 17, 2021 12:00 PM

“1. The employer failed to notify employees and exclude them from the workplace after being exposed to a COVID-19 case while in the workplace. T8 CCR 3205(c)(10)(B) & (c)(3)(B)3. 2. The employer failed to report information regarding a COVID-19 case at the workplace to the local health department. T8... See MoreCCR 3205(c)(9)(A)

Alleged Hazards: 2, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-02-01
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Donut Petit, 711 Santa Clara Avenue, ALAMEDA, CA, 94501, USA

Donut Petit, 711 Santa Clara Avenue, ALAMEDA, CA, 94501, USA

March 17, 2021 12:00 PM

“1. The employer failed to notify employees and exclude them from the workplace after being exposed to a COVID-19 case while in the workplace. T8 CCR 3205(c)(10)(B) & (c)(3)(B)3. 2. The employer failed to report information regarding a COVID-19 case at the workplace to the local health department. T8... See MoreCCR 3205(c)(9)(A)

Alleged Hazards: 2, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-02-01
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walgreens #9248, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

Walgreens #9248, 2300 Otis Drive, ALAMEDA, CA, 94501, USA

March 17, 2021 12:00 PM

“1. The employer has not ensured that employees are separated from other persons by at least six feet in the Pharmacy Department. T8 CCR 3205(c)(6) 2. The employer has not excluded employees who had exposure to two known COVID-19 cases from the workplace for at least 10 days. Due to the employees in... See Morethe pharmacy department working in close proximity, many of these employees had exposure to the two known COVID-19 cases. T8 CCR 3205(c)(10)(B) 3. The employer did not disinfect the areas, material, and equipment used by COVID-19 cases in the workplace. T8 CCR 3205(c)(8) 4. The employer failed to engage in adequate and effective infection prevention and to implement the proper control measures to protect its workers from COVID-19 hazards. On 1/14/21, an employee tested positive for COVID-19. That employee worked 8 hours the previous day and exposed at least five other employees. The employer require those employees to report to work without testing or quarantine. T8 CCR 3205(c)

Alleged Hazards: 4, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-01-25
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Reported By SafelyHQ.com User

Recent Interesting Reports

Moderna vaccine first shot, Sayville, NY, USA

Symptoms: Numbness Fatigue Soreness
Sayville, NY, USA

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
Reported By SafelyHQ.com User

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
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Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User
Vaccine Side Effects Special summary

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
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Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User

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
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Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Salmonella

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
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Reported By SafelyHQ.com User

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
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Reported By SafelyHQ.com User

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. .
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Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User