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Safety Reports: Recall

Updated: February 8, 2022 9:04 PM

Real Time Reports

Recall notice

Red Mammoth Capsules - recalled due to undeclared Sildenafil and Tadalafil, USA

4 years ago •source fda.gov • details

Celebrate Today is voluntarily recalling lot number DK1027, Exp 08/01/2023 of Red Mammoth capsules to the consumer level. Celebrate Today was informed by Amazon that laboratory analysis has found the product to be tainted with sildenafil and tadalafil, ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA… See more

#vitamins #blood #recall #unitedstates

Recalls Red Mammoth Capsules - recalled due to undeclared Sildenafil and Tadalafil Celebrate Today is volunt... photo #1

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Recall notice

MAC DADDY DIETARY SUPPLEMENTS - recalled due to undeclared Sildenafil & Tadalafil, USA

4 years ago •source fda.gov • details

ABC SALES 1 INC is voluntarily recalling MAC DADDY RED Capsules, Lot 1230004, Exp 03/30/2024 and MAC DADDY PURPLE Capsules, Lot 1230005, Exp 03/30/2024 to the consumer level. ABC Sales 1 Inc was informed by Amazon that laboratory analysis found MAC DADDY RED capsules to be tainted… See more

#blood #recall #drugs #unitedstates

Recalls MAC DADDY DIETARY SUPPLEMENTS - recalled due to undeclared Sildenafil & Tadalafil ABC SALES 1 INC is... photo #1

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Recall notice

Your Favorite Shop The Red Pill - recalled due to undeclared Tadalafil, USA

4 years ago •source fda.gov • details

Your Favorite Shop is voluntarily recalling lot # 26436989. Expiry 10/30/2023 of The Red Pill, packaged in 10-count blisters packaged in a carton to the consumer level. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com nationwide in the USA.

Your Favorite Shop… See more

#blood #recall #drugs #unitedstates

Recalls Your Favorite Shop The Red Pill - recalled due to undeclared Tadalafil Your Favorite Shop is volunta... photo #1

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Recall notice

STANDARD Q COVID-19 Ag Home Test - recalled due to illegally imported into the US, USA

4 years ago •source fda.gov • details

SD Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed reports that the test kits were illegally imported into the United States. The STANDARD Q COVID-19 Ag Home Test is not authorized,… See more

#recall #medicaldevices #unitedstates

Recalls STANDARD Q COVID-19 Ag Home Test - recalled due to illegally imported into the US SD Biosensor, Inc.... photo #1

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Recall notice

Vyaire Medical ventilators - recalled due technical failure alarm, USA

4 years ago •source fda.gov • details

Imtmedical ag, a subsidiary of Vyaire Medical, initiated a voluntary field correction for certain bellavista™ ventilators. With specific software version and configuration combinations, the ventilators can cease ventilation and generate a technical failure alarm 305. There is a potential issue with bellavista™ 1000 and 1000e ventilators that… See more

#recall #medicaldevices #unitedstates

Recalls Vyaire Medical ventilators - recalled due technical failure alarm Imtmedical ag, a subsidiary of Vya... photo #1

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Recall notice

MegMan Performance Booster capsules - recalled due to undeclared Tadalafil, USA

4 years ago •source fda.gov • details

Junp LLC is voluntarily recalling Lot number 2010291, Exp Date: 01/07/2024 of MegMan Performance Booster capsules, packaged in 10-count blisters packaged in a carton to the consumer level. Junp LLC was notified by Amazon that laboratory analysis has found the product to be tainted with Tadalafil.

Tadalafil… See more

#recall #blood #amazon #drugs #unitedstates

Recalls MegMan Performance Booster capsules - recalled due to undeclared Tadalafil Junp LLC is voluntarily r... photo #1

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Recall notice

Hard Dawn Rise and Shine capsules - recalled due to Undeclared Tadalafil, USA

4 years ago •source fda.gov • details

Esupplementsales, LLC is voluntarily recalling lot number 2107 of Hard Dawn Rise and Shine capsules to the consumer level. Esupplementsales, LLC was informed by Amazon that laboratory analysis has found the product to be tainted with tadalafil, which renders the product an unapproved drug for which safety… See more

#blood #recall #drugs #unitedstates

Recalls Hard Dawn Rise and Shine capsules - recalled due to Undeclared Tadalafil Esupplementsales, LLC is vo... photo #1

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Recall notice

AuroMedics Polymyxin B for Injection USP, 500,000 Units/Vial - recalled due to Particulate Matter, USA

4 years ago •source fda.gov • details

East Windsor, New Jersey, AuroMedics Pharma LLC has initiated a voluntary recall of lot number CPB200013 of Polymyxin B for Injection USP, 500,000 Units/Vial, to the consumer level from the USA market due to a product complaint for the presence of particulate matter, identified as hair being… See more

#recall #drugs #unitedstates #cake

Recalls AuroMedics Polymyxin B for Injection USP, 500,000 Units/Vial - recalled due to Particulate Matter Ea... photo #1

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Recall notice

RevitaDerm Wound Care Gel - recalled due to Bacillus cereus contamination, USA

4 years ago •source fda.gov • details

Blaine Labs Company is voluntarily recalling one lot of RevitaDerm Wound Care to the consumer level because a bottle of the 1.0 ounce RevitaDerm Wound Care Gel has been found to be contaminated with Bacillus cereus.

Risk Statement: Patients who apply the contaminated product to a wound… See more

#blood #recall #drugs #unitedstates

Recalls RevitaDerm Wound Care Gel - recalled due to Bacillus cereus contamination Blaine Labs Company is vol... photo #1

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Recall notice

Semglee Insulin glargine injection, 100 units/ml (U-100), 3mL prefilled pens - recalled due to Missing Label, USA

4 years ago •source fda.gov • details

Mylan Pharmaceuticals Inc., a Viatris company, is voluntarily recalling one batch of its non-interchangeable Semglee® (insulin glargine injection), 100 units/ml (U-100), 3mL prefilled pens, which are packaged in a labelled carton of five (5) pens. The product is being recalled due to the potential for the label… See more

#blood #recall #drugs #unitedstates #sugar

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Safety Reports: Recall

Real Time Reports

Red Mammoth Capsules - recalled due to undeclared Sildenafil and Tadalafil, USA

MAC DADDY DIETARY SUPPLEMENTS - recalled due to undeclared Sildenafil & Tadalafil, USA

Your Favorite Shop The Red Pill - recalled due to undeclared Tadalafil, USA

STANDARD Q COVID-19 Ag Home Test - recalled due to illegally imported into the US, USA

Vyaire Medical ventilators - recalled due technical failure alarm, USA

MegMan Performance Booster capsules - recalled due to undeclared Tadalafil, USA

Hard Dawn Rise and Shine capsules - recalled due to Undeclared Tadalafil, USA

AuroMedics Polymyxin B for Injection USP, 500,000 Units/Vial - recalled due to Particulate Matter, USA

RevitaDerm Wound Care Gel - recalled due to Bacillus cereus contamination, USA

Semglee Insulin glargine injection, 100 units/ml (U-100), 3mL prefilled pens - recalled due to Missing Label, USA

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