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Safety Reports: Blood

Updated:

Real Time Reports

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

3 years ago •source fda.gov • details

Recall notice

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

#dietarysupplements #recall #blood #unitedstates

Red Mammoth Capsules - recalled due to undeclared Sildenafil and Tadalafil photo #1
  Comments Comment

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

3 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #blood #unitedstates

MAC DADDY DIETARY SUPPLEMENTS - recalled due to undeclared Sildenafil & Tadalafil photo #1
  Comments Comment

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

3 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #blood #unitedstates

Your Favorite Shop The Red Pill - recalled due to undeclared Tadalafil photo #1
  Comments Comment

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

3 years ago •source fda.gov • details

Recall notice

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

#drugs #amazon #recall #blood #unitedstates

MegMan Performance Booster capsules - recalled due to undeclared Tadalafil photo #1
  Comments Comment

Hard Dawn Rise and Shine capsules - recalled due to undeclared tadalafil, USA

3 years ago •source fda.gov • details

Recall notice

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, an ingredient known as a phosphodiesterase (PDE-5) inhibitor found in… See more

#drugs #blood #unitedstates

Hard Dawn Rise and Shine capsules - recalled due to undeclared tadalafil photo #1
  Comments Comment

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

3 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #blood #unitedstates

Hard Dawn Rise and Shine capsules - recalled due to Undeclared Tadalafil photo #1
  Comments Comment

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

3 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #blood #unitedstates

RevitaDerm Wound Care Gel - recalled due to Bacillus cereus contamination photo #1
  Comments Comment

Covid-19 OSHA Complaint, Sharp Grossmont Hospital, 5555 Grossmont Center Drive, LA MESA, CA, 91942, USA

3 years ago • details

Regulatory Report

T8 CCR 5193(f)(3)(C) The employer did not provide for collection and testing of employee's blood for HBV, HCV and HIV serological status consent was obtained from the employee who sustained a needlestick injury. T8 CCR 51963(f)(3)(B)(3) The result of the source individual's testing was not made available… See more

#coronaviruscovid19 #osha #blood #5555grossmontcenterdrive #lamesa #california #unitedstates

  Comments Comment

Covid-19 OSHA Complaint, Wendy's, 1200 Eagle Drive, LOVELAND, CO, 80537, USA

3 years ago • details

Regulatory Report

1. Employees are potentially exposed to the health hazards associated with COVID-19. It was reported to OSHA that this establishment has had four confirmed cases of COVID-19 and that the employer did not conduct contact tracing or notify those employees who had close contact. Contrary to Section… See more

#coronaviruscovid19 #osha #wendys #blood #1200eagledrive #loveland #colorado #unitedstates

  Comments Comment

Covid-19 OSHA Complaint, PREMIER PROCESSING LLC, 3002 W PAWNEE ST, SUITE 104, WICHITA, KS, 67213, USA

3 years ago • details

Regulatory Report

Location is in the paint booths: 1. Supplied airhood used, fresh air has stopped flowing and employee(s) have difficulties to breathe. 2. Not performing blood testing for hexavalent chromium. 3. No fit- testing for respirator use nor medical surveillance. 4. Chromium out all over the floor. 4.… See more

#coronaviruscovid19 #osha #blood #3002westpawneestreet #wichita #kansas #unitedstates

  Comments Comment

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