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Antioch, California, United States

Updated: March 24, 2021 12:00 PM

Covid-19 OSHA Complaint, Geno's Auto Body, 1825 West 10th Street, ANTIOCH, CA, 94509, USA

Geno's Auto Body, 1825 West 10th Street, ANTIOCH, CA, 94509, USA

March 24, 2021 12:00 PM

“1. The employer did not ensure to exclude COVID-19 cases from the workplace until the return to work criteria subsection (c)(11) has been met. T8 CCR 3205(c)(10)(A). 2. The employer did not give notice to employees on their potential exposure to a COVID-19 positive case. T8 CCR 3205(c)(3)(B)(3). 3.... See MoreThe employer did not ensure to exclude employees with a COVID-19 exposure from the workplace for 10 days from date of last exposure. T8 CCR 3205(c)(10)(B). 4. The employer did not ensure employees are wearing facial coverings properly. T8 CCR 3205(c)(7)(A). 5. The employer did not ensure employees can maintain a physical distance of at least 6 feet between other persons while in meetings or in work spaces. T8 CCR 3205(c)(6). 6. The employer did not ensure that walking and working surfaces are free from dangerous projections and other hazard such as sharp blades. T8 CCR 3273(a).

Alleged Hazards: 6, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-24
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Tri Delta Transit, 801 Wilbur Avenue, ANTIOCH, CA, 94509, USA

Tri Delta Transit, 801 Wilbur Avenue, ANTIOCH, CA, 94509, USA

March 24, 2021 12:00 PM

“1. The employer did not ensure that all machinery and equipment are maintained in accordance with the manufacturers recommendations. T8 CCR 3328(b). 2. The employer did not ensure that permanent working surfaces are maintained free of oils and grease to prevent slipping hazards to employees working... See Morein the area. T8 CCR 3373(a). 3. The employer did not implement a cleaning and disinfecting procedure to disinfect high touch surfaces/objects on their buses. T8 CCR 3205(c)(8)(c).

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-12
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Contra Costa County Employment & Human Services, 4545 Delta Fair Blvd, ANTIOCH, CA, 94509, USA

Contra Costa County Employment & Human Services, 4545 Delta Fair Blvd, ANTIOCH, CA, 94509, USA

March 10, 2021 12:00 PM

“1. The employer did not give notice to employees on their potential exposure to a COVID-19 positive case. T8 CCR 3205(c)(3)(B)(3). 2. The employer did not ensure to exclude employees from the workplace who have been exposed to a positive COVID-19 case. T8 CCR 3205(c)(10)(B). 3. The employer did not... See Moreensure to conduct an evaluation of the indoor HVAC system and to increase filtration efficiency to the highest level compatible with the existing ventilation system. T8 CCR 3205(c)(2)(E). 4. The employer did not implement an effective cleaning and disinfecting procedure to disinfect high touch surfaces and objects. T8 CCR 3205(c)(8)(c). 5. The employer did not implement an effective policy and/or procedure to correct the unsafe/unhealthy condition of allowing employees who are at a higher risk of having negative outcome should they contract COVID-19 by denying those employees access to their work from home program. T8 CCR 3205(c)(4).

Alleged Hazards: 5, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-03
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Reported By SafelyHQ.com User
Vaccine Side Effects Special summary

Covid-19 OSHA Complaint, Delta Dispensary Inc., 2101 W. 10th Street, Ste J, ANTIOCH, CA, 94509, USA

Delta Dispensary Inc., 2101 W. 10th Street, Ste J, ANTIOCH, CA, 94509, USA

February 3, 2021 12:00 PM

“Employees don't wear masks while not visible to the public and wear masks improperly a lot of the times. Also, they don't maintain physical distance in breakroom and there are no physical barriers to protect employees from customers. 1. The employer did not ensure employees are wearing facial coveri... See Morengs properly. T8 CCR 3205(c)(7)(A). 2. The employer did not ensure employees can maintain a physical distance of at least 6 feet between other persons. T8 CCR 3205(c)(6). 3. The employer did not ensure that effective barriers were installed to reduce the risk of transmission between patrons and employees. T8 CCR 3205(c)(8)(A).

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-17
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, McDonald's, 914 Main Street, OAKLEY, CA, 94561, USA

McDonald's, 914 Main Street, OAKLEY, CA, 94561, USA

January 21, 2021 12:00 PM

“1. The employer is not ensuring that COVID-19 cases are excluded from work. T8 CCR 3205(c)(10)(A). 2. The employer is not ensuring that COVID-19 cases only return to work once the return to work criteria has been met. T8 CCR 3205(c)(11).

Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov |... See MoreReceipt Date: 2020-12-21 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Antioch Nissan, 1831 Auto Center Drive, ANTIOCH, CA, 94509, USA

Antioch Nissan, 1831 Auto Center Drive, ANTIOCH, CA, 94509, USA

January 14, 2021 12:00 PM

“The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer is not ensu... See Morering that COVID-19 cases are excluded from work and return only once the return to work criterion have been met, T8 CCR 3205(c)(11).

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-21
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Victory Fire Protection, Inc., 5083 Lone Tree Way, ANTIOCH, CA, 94531, USA

Victory Fire Protection, Inc., 5083 Lone Tree Way, ANTIOCH, CA, 94531, USA

January 14, 2021 12:00 PM

“The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not ens... See Moreure employees are wearing facial coverings properly, T8 CCR 3205(c)(7)(A). 2. The employer did not ensure employees maintain a physical distance of at least 6 ft. between each other, T8 CCR 3205(c)(6)(A). 3. The employer did not develop ad implement a screening process to respond to employees with COVID-19 symptoms, T8 CCR 3205(c)(2)(B).

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-21
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Contra Costa Farms (CoCo Farms), 3400 Wilbur Avenue, ANTIOCH, CA, 94509, USA

Contra Costa Farms (CoCo Farms), 3400 Wilbur Avenue, ANTIOCH, CA, 94509, USA

January 14, 2021 12:00 PM

“The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not ens... See Moreure to exclude employees from the work place who have tested positive for COVID-19, T8 CCR 3205(c)(10)(B). 2. The establishment has ineffective barriers, T8 CCR 3205(c)(10)(A). 3. The employer did not implement disinfecting barriers, T8 CCR 3205(c)(8). 4. The employer did not implement specific disinfecting protocols for areas where positive COVID-19 cases worked, touched or had been in contact with, T8 CCR 3205(c)(8)(C)(3). 5. The employer did not ensure to reduce the number of patrons to allow for a physical distance of at least 6 ft. between persons at all times, T8 CCR 3205(c)(6)(A).

Alleged Hazards: 5, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-07
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Georgia-Pacific Corporation LLC, 801 Minaker Drive, ANTIOCH, CA, 94509, USA

Georgia-Pacific Corporation LLC, 801 Minaker Drive, ANTIOCH, CA, 94509, USA

January 14, 2021 12:00 PM

“The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not ens... See Moreure that high touch surfaces and areas touched or worked in by positive COVID-19 cases were properly disinfected, T8 CCR 3205(c)(8)(C).

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-04
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Taco Bell, 3445 Deer Valley Road, ANTIOCH, CA, 94531, USA

Taco Bell, 3445 Deer Valley Road, ANTIOCH, CA, 94531, USA

January 14, 2021 12:00 PM

“The employer did not maintain an effective Injury and Illness Prevention Program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not tra... See Morein employees on how to limit the spread of COVID-19, including how to screen themselves for symptoms and stay home if they them. T8 CCR 3203(a)(7). 2. The employer did not implement individual control measures and screenings. T8 CCR 3203(a)(6). 3. The employer did not implement handwashing protocols. T8 CCR 3203(a)(6). 4. The employer did not ensure masks or other personal protective equipment are being properly used. T8 CCR 3203(a)(4)(6).

Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-30
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Reported By SafelyHQ.com User

Recent Interesting Reports

Pfizer First Dose Vaccine, Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

Symptoms: Headache Fatigue Soreness
Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

April 2, 2021 7:33 PM

“The vaccine process went relatively smooth. Waited the recommended 15 minutes for any allergic reactions. Had none. My side effects have been mild. Headache, run down feeling, head fogginess, sore arm from where the vaccine was injected, alittle fatigued, and have noticed my heart rate being alittle... See Moretoo high for comfort. See Less
Reported By SafelyHQ.com User

April 5, 2021 4:16 PM

“I ordered a Stihl battery operated hand held saw off the internet for $37.00 and got a chain with 2 cloth handles. I would like my saw or money back. See Less
Reported By SafelyHQ.com User

April 7, 2021 11:00 AM

“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: Cliffside Park, NJ, Yol... See Moreo Studio is voluntarily recalling all lots of PremierZEN Extreme 3000, PremierZEN Black 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 Black 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 Black 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 Black 5000, & Triple SupremeZEN Plus 3500 include all lots. PremierZEN Extreme 3000, PremierZEN Black 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 Black 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. 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
Vaccine Side Effects Special summary

March 25, 2021 9:01 AM

“Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Antimicrobial Hand Sanitizer
Reason of the recall: Due to microbial contamination
FDA Recall date: March 24, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan announces a voluntary recall of the lot... See Mores listed in the table below of Durisan Antimicrobial Hand Sanitizer, Non-Alcohol products in various sizes listed. The products are being recalled due to microbial contamination. Specifically, out of specification results for bacterial count for Burkholderia cepacia complex and Ralstonia pickettii. The issue was discovered during a routine audit focused on production scale-up during the height of the pandemic.

Check the link below for the full list of Durisan Antimicrobial Solutions Hand Sanitizer Sizes and Lot Numbers. To date, no reports of adverse reactions or customer complaints have been reported related to this recall.

The product was packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. Pictures are available in the attached related file.

Use of a hand sanitizer contaminated with Burkholderia cepacia complex and Ralstonia pickettii, can range from no reaction to serious infections in a person with a hand wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems. Health care professionals who use this contaminated hand sanitizer and tend to an at-risk patient, such as one with cystic fibrosis, could lead to adverse events ranging from a localized infection to lung or bloodstream infections, which could require patient hospitalization.

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. The product can be identified by examples of the product labels below. The product was manufactured from Feb. 1, 2020 until June 30, 2020, and distributed to selected retailers nationwide in the United States.

Durisan has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. Consumers that have the product which is being recalled are advised to destroy it immediately.

Consumers with questions regarding this recall can contact Durisan at 941-351-9114 [Call: 941-351-9114] , 8:30 am - 4:30 pm Eastern time, Monday through Friday or by e-mail at customerservice@durisan.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.

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

March 23, 2021 5:59 PM

“All I received was the chain and straps not the chain saw how can I get my money back? I am 73 and got cheated out of $29.99 plus tax for a chain saw when all I received was a chain and I want my money back See Less
Reported By SafelyHQ.com User

March 17, 2021 11:00 AM

“Company name: PNHC, LLC d/b/a Heal the World
Brand name: Heal the World
Product recalled: Hand Sanitizer
Reason of the recall: Because they resemble water bottles; risk of ingestion
FDA Recall date: March 17, 2021
Recall details: Raleigh, North Carolina, PNHC, LLC, d/b/a Heal the World, is vol... See Moreuntarily recalling all lots of Heal the World hand sanitizer packaged in 9.6 fl. oz containers to the consumer level. The products are being recalled because they resemble 9.6ounce water bottles. The recall does not affect any other Hand Sanitizer products from PNHC, LLC and/or Heal the World.

- Heal the World Hand Sanitizer (9.6 FL. OZ (285 mL)). NDC: 73333-285-01. Lot Nos. SAA21, SAA24, SAA27, SAA22, SAA23, SAA29, SAA26, SAA28, SAA25, SAA32, SAA55, SAA56, SAA44, SAA60.

To date, PNHC, LLC, d/b/a Heal the World has received no reports of adverse reactions and no complaints have been received. Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute.

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 9.6 ounce plastic bottles. The product can be identified by the bottle’s label pictured below. Product was distributed to selected retailers in the United States.

PNHC, LLC has provided notification to its distributors and retailers. Distributors and retailers that have product which is being recalled should stop distribution. While the product is not available for purchase and has not been available for several months, if a consumer has product which is being recalled he or she is advised to contact the entity who sold the product to consumer for return.

Consumers with questions regarding this recall can contact PNHC, LLC at 813-434-0741 from 9:00 am- 5:00 pm EST, Monday through Friday. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

March 26, 2021 7:00 PM

“Company name: Namoo Enterprise LLC
Brand name: PremierZen
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 26, 2021
Recall details: Little Ferry, NJ, Namoo Enterprise LLC is voluntarily recalling al... See Morel lots within expiry of PremierZen Black 5000 capsules to the consumer level. FDA analysis has found the product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil, known as phosphodiesterase (PDE-5) inhibitors, are found in FDA approved products for the treatment of male erectile dysfunction.

The presence of sildenafil and tadalafil in PremierZen Black 5000 products makes them unapproved new drugs for which the safety and efficacy have not been established and therefore subject to recall. Risk Statement: Consumers with underlying medical issues who take PremierZen Black 5000 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, Namoo Enterprise LLC has not received any reports of adverse events related to this recall. The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in card form with one capsule per card and is aware of at least one lot with an expiration date of December 2023. Each pack is black with gold, blue, white and red text. The capsule appears black and is enclosed within clear plastic on the package. The affected lots of PremierZen Black 5000 includes all lots. PremierZen Black 5000 was sold nationwide in the USA via the internet and fulfilled by ebay at www.ebay.com and also fulfilled by amazon at www.amazon.com.

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. Namoo Enterprise LLC is notifying its customers by this press announcement and by mailing recall letters. Consumers that have PremierZen Black 5000 should stop using and destroy them. Consumers with questions regarding this recall can contact Namoo Enterprise LLC by phone at 201-267-0539, Monday to Friday, 9 A.M. to 5 P.M. EST or email at namooenterprise@gmail.com from Monday to Friday.

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. 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 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

J&J one shot vaccine, Valencia, Santa Clarita, CA, USA

Symptoms: Nausea Fever Headache Chills Soreness
Valencia, Santa Clarita, CA, USA

April 5, 2021 7:15 PM

“Recieved my shot on 4/1/21 @ 2pm. By 10pm had a headache. Middle of the night low grade fever, chills, and nausea. Lasted 48 hours. Now 5 days out and still redess, soreness, and lump at injection site. See Less
Reported By SafelyHQ.com User