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Safety Reports: Drugs

Updated: September 29, 2022 9:00 PM

Real Time Reports

Recall notice

Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up, USA

3 years ago •source fda.gov • details

Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This voluntary… See more

#blood #recall #drugs #unitedstates

Recalls Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up Golden State Medic... photo #1

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Recall notice

My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil, USA

3 years ago •source fda.gov • details

Proper Trade LLC/My Stellar Lifestyle is voluntarily recalling Wonder Pill lot 20210912 and lot 31853-501, expiry 09/24, packaged in 10-count blisters co-packaged in a carton and in 60-count bottles to the consumer level. Proper Trade LLC/My Stellar Lifestyle was notified by Amazon that laboratory analysis has found… See more

#blood #recall #drugs #unitedstates #sub #ro-tel

Recalls My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil Proper Trade LLC/My... photo #1

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Recall notice

Auromedics Acyclovir Intravenous Product - recalled due to particulate inside the vial, USA

3 years ago •source fda.gov • details

East Windsor, New Jersey, Eugia US LLC (formerly AuroMedics Pharma LLC) has initiated a voluntary recall of lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial to the consumer level from the U.S. market due to… See more

#drugs #unitedstates #ro-tel

Recalls Auromedics Acyclovir Intravenous Product - recalled due to particulate inside the vial East Windsor,... photo #1

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Recall notice

Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene, Seattle, WA, USA

3 years ago •source fda.gov • details

Salon Technologies International. Inc. is voluntarily recalling one lot of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A. Expiration 6/18/2023 to the consumer level. Firm lab testing has found the product to contain benzene. Benzene is classified as a human carcinogen. Exposure to benzene can… See more

#blood #drugs #seattle #washington #unitedstates

Recalls Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene Salon Techn... photo #1

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Recall notice

Family Dollar Toothpaste - recalled due to storage outside of labeled temperature, USA

3 years ago •source fda.gov • details

Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to a limited number of stores in AZ, CA, GA, ID, IN, MT, NM, NV, OR, TX, and UT on… See more

#familydollar #drugs #truckton #colorado #unitedstates

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Recall notice

Propofol Injection Emulsion, USP - recalled due to the presence of particulates, USA

3 years ago •source fda.gov • details

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion (containing benzyl alcohol), 100mL Single Patient Use Glass Fliptop Vial; lot EA7470, to the user level due to visible particulates observed in two vials during annual examination of retention samples. The product lot… See more

#pfizer #blood #drugs #unitedstates #pita

Recalls Propofol Injection Emulsion, USP - recalled due to the presence of particulates Hospira, Inc., a Pfi... photo #1

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Recall notice

Magnesium Citrate Saline Laxative Oral Solution - recalled due to microbial contamination, USA

3 years ago •source fda.gov • details

Vi-Jon, LLC is revising a previously reported list of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry that were voluntarily recalled to the consumer level to include product that was distributed in the United States, Canada and Panama. This includes all lots of Cherry… See more

#recall #drugs #unitedstates #lemon #patio

Recalls Magnesium Citrate Saline Laxative Oral Solution - recalled due to microbial contamination Vi-Jon, LL... photo #1

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Recall notice

Major Milk of Magnesia, Magnisium Hydroxide/Aluminum Hydroxide/Simethicone Oral Suspension - recalled due to microbial contamination, USA

3 years ago •source fda.gov • details

Plastikon Healthcare, LLC is issuing an update to the voluntary recall initiated on June 3, 2022. The recall has been expanded to include Lot 20076A of Magnesium Hydroxide 1200 mg / Aluminum Hydroxide 1200 mg / Simethicone 120 mg per 30 mL Oral Suspension. The products are… See more

#recall #drugs #unitedstates #pita #sub #milk #chi-chis #patio

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Recall notice

SANGTER Energy Supplement - recalled due to Undeclared Sildenafil, USA

3 years ago •source fda.gov • details

DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to the consumer level. FDA analysis has found the product to contain undeclared sildenafil. Sildenafil is a phosphodiesterase (PDE-5) inhibitor found in FDA-approved… See more

#blood #recall #drugs #unitedstates #sub

Recalls SANGTER Energy Supplement - recalled due to Undeclared Sildenafil DISTRIBUTOR RFR, LLC. is voluntari... photo #1

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Recall notice

Vi-Jon, LLC Magnesium Citrate Saline Laxative Oral Solution - recalled due to bacterial contamination, USA

3 years ago •source fda.gov • details

Smyrna, TN, Vi-Jon, LLC is expanding its voluntary recall to include all lots of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry to the consumer level. This expansion includes all lots of Cherry Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution,… See more

#recall #drugs #unitedstates #lemon #patio