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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Teva Pharmaceuticals Injection USP - recalled due to particulate matter, USA

3 years ago •source fda.gov • details

Teva Pharmaceuticals has initiated a voluntary nationwide recall of lot 31329657B of IDArubicin Hydrochloride Injection USP 5 mg/5 mL vial, to the user level in the United States. This voluntary recall is initiated based on an internal inspection that found particulate matter in one vial of the… See more

#drugs #blood #unitedstates #sub

Recalls Teva Pharmaceuticals Injection USP - recalled due to particulate matter Teva Pharmaceuticals has ini... photo #1
312   Comments Comment

Recall notice

Major Pharmaceuticals Drugs - recalled due to microbial contamination, USA

3 years ago •source fda.gov • details

Plastikon Healthcare, LLC is voluntarily recalling three (3) lots of Milk of Magnesia 2400 mg/30 mL Oral Suspension, one (1) lot of Acetaminophen 650mg/ 20.3mL, and six (6) lots of Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/Simethicone 120mg per 30 mL to the hospital, clinic and patient level. The… See more

#drugs #unitedstates #milk

Recalls Major Pharmaceuticals Drugs - recalled due to microbial contamination Plastikon Healthcare, LLC is v... photo #1
312   Comments Comment

Recall notice

Reckitt Airborne Gummies - recalled due to injury hazard, USA

3 years ago •source cpsc.gov • details

Reckitt has announced a recall of its Airborne Gummies (63 and 75 count bottles) sold in blueberry pomegranate, orange and assorted fruit flavors due to injury hazard, when opened for the first time, pressure build up in the bottle can cause the cap and underlying seal to… See more

#samsclub #costco #walmart #bjs #target #walgreens #amazon #drugs #cvspharmacy #unitedstates #fruit #orange

Recalls Reckitt Airborne Gummies - recalled due to injury hazard Reckitt has announced a recall of its Airbo... photo #1
312   Comments Comment

Recall notice

Pfizer Accuretic™, quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets - recalled due to N-NitrosoQuinapril, USA

3 years ago •source fda.gov • details

Pfizer is voluntarily recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets distributed by Pfizer as well as two authorized generics distributed by Greenstone (quinapril and hydrochlorothiazide and quinapril HCl/ hydrochlorothiazide) to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-quinapril, above the Acceptable Daily Intake (ADI) level.… See more

#drugs #recall #pfizer #blood #unitedstates #vegetable #meat #ro-tel

Recalls Pfizer Accuretic™, quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets... photo #1
312   Comments Comment

Recall notice

SYMJEPI Injection Pre-Filled Single-Dose Syringes - recalled due to potential clogging of the needle, USA

3 years ago •source fda.gov • details

Adamis Pharmaceuticals Corporation (Nasdaq: ADMP) is voluntarily recalling certain lots of SYMJEPI (epinephrine) Injection 0.15 mg (0.15 mg/0.3 mL) and 0.3 mg (0.3 mg/0.3 mL) Pre-Filled Single-Dose Syringes to the consumer level. The batches in the table below are being recalled due to the potential clogging of… See more

#drugs #recall #unitedstates #sub

Recalls SYMJEPI Injection Pre-Filled Single-Dose Syringes - recalled due to potential clogging of the needle... photo #1
312 1 Share   Comments Comment

Recall notice

Sandoz Orphenadrine Citrate 100 mg Extended Release (ER) Tablets - recalled due to a Nitrosamine Impurity, USA

3 years ago •source fda.gov • details

Sandoz Inc. (“Sandoz”) is initiating a voluntary recall of 13 lots (listed below) of oral Orphenadrine Citrate 100 mg Extended Release (ER) Tablets to the consumer level. The presence of a nitrosamine (N-methyl-N-nitroso-2-[(2-methylphenyl)phenylmethoxy]ethanamine (NMOA or Nitroso-Orphenadrine)) impurity, which has the potential to be above the U.S. Food… See more

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

Recalls Sandoz Orphenadrine Citrate 100 mg Extended Release (ER) Tablets - recalled due to a Nitrosamine Imp... photo #1
312   Comments Comment

Recall notice

Olympia Pharmacy Compounded Injectables - recalled due to products are out of specification, USA

3 years ago •source fda.gov • details

Olympia Pharmacy is voluntarily recalling 11 specific lots of Trimix Formulas F-9, T-105, SB-4, Sermorelin, Sincalide, Hydroxocobalamin, and NAD, compounded injectables to the consumer level. These compounded products were found to be out-of-specification.

The affected lots include the following lot numbers and expiration dates listed below. The… See more

#drugs #recall #unitedstates #sub

Recalls Olympia Pharmacy Compounded Injectables - recalled due to products are out of specification Olympia... photo #1
313   Comments Comment

Recall notice

Tennessee Technical Coatings Corp. Hand Sanitizer - recalled due to Product contains methanol, Tennessee, USA

3 years ago •source fda.gov • details

Tennessee Technical Coatings Corp. is voluntarily recalling all lots of HAND SANITIZER Isopropyl Alcohol Antiseptic 75% to the consumer/user level. FDA analysis has found the product to contain methanol. To date, Tennessee Technical Coatings Corp. has not received any reports of adverse events related to this recall.… See more

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

Recalls Tennessee Technical Coatings Corp. Hand Sanitizer - recalled due to Product contains methanol Tennes... photo #1
107   Comments Comment

Recall notice

Fresenius Kabi Sodium Acetate Injection, USP - recalled due to Particulate Matter, USA

3 years ago •source fda.gov • details

Fresenius Kabi USA is voluntarily recalling seven lots of Sodium Acetate Injection, USP, 400 mEq/100 mL (4 mEq/mL), 100 mL fill in a 100 mL vial to the user level due to the presence of particulate matter found in reserve and/or stability sample vials. Microscopic and elemental… See more

#drugs #blood #unitedstates #pita

Recalls Fresenius Kabi Sodium Acetate Injection, USP - recalled due to Particulate Matter Fresenius Kabi USA... photo #1
312   Comments Comment

Recall notice

B. Braun Medical Inc. 0.9% Sodium Chloride for Injection USP 250ML in Excel - recalled due to Fluid Leakage, USA

3 years ago •source fda.gov • details

B. Braun Medical Inc. (B. Braun) is voluntarily recalling five (5) lots of 0.9% Sodium Chloride for Injection USP 250ML in Excel within the United States to the hospital/user level. The biggest risk with a slow leak in any intravenous solution preparation is a break in sterility… See more

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

Recalls B. Braun Medical Inc. 0.9% Sodium Chloride for Injection USP 250ML in Excel - recalled due to Fluid... photo #1
312   Comments Comment

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