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Safety Reports: Drugs

Updated:

Aurobindo Pharma Quinapril and Hydrochlorothiazide Tablets - recalled due to due to presence of impurities, USA

1 year ago •source fda.gov • details

Recall notice

East Windsor, New Jersey, Aurobindo Pharma USA, Inc. has initiated a voluntary recall of two (2) lots (refer table below) of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, to the consumer level from the US market due to presence of Nitrosamine Drug Substance Related Impurity (NDSRI),… See more

#blood #drugs #us #sub #vegetable #meat #ro-tel

Aurobindo Pharma Quinapril and Hydrochlorothiazide Tablets - recalled due to due to presence of impurities photo #1
321

Exela & Civica Sodium Bicarbonate Injection - recalled due to vial breakage, USA

1 year ago •source fda.gov • details

Recall notice

Exela Pharma Sciences, LLC, (Exela) is voluntarily recalling 49 lots of Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL vial, 20count carton, to the consumer level. Product was distributed nationwide to wholesalers, distributors, and other customers between December 16, 2021 and August 10, 2022.

Risk Statement: The… See more

#recall #drugs #us #corn #sub

Exela & Civica Sodium Bicarbonate Injection - recalled due to vial breakage photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us

Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us #sub #ro-tel

My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us #ro-tel

Auromedics Acyclovir Intravenous Product - recalled due to particulate inside the vial photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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

#drugs #blood #seattle #washington #us

Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene photo #1
1.1K

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

1 year ago •source fda.gov • details

Recall notice

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 #us

Family Dollar Toothpaste - recalled due to storage outside of labeled temperature photo #1

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

1 year ago •source fda.gov • details

Recall notice

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

#blood #pfizer #drugs #us #pita

Propofol Injection Emulsion, USP - recalled due to the presence of particulates photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us #lemon #patio

Magnesium Citrate Saline Laxative Oral Solution - recalled due to microbial contamination photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us #pita #sub #milk #chi-chis #patio

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