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Safety Reports: Drugs

Updated: December 27, 2022 11:00 AM

Real Time Reports

Recall notice

Accord Daptomycin for Injection - recalled due to mislabeling, USA

3 years ago •source fda.gov • details

Durham, North Carolina, Accord Healthcare, Inc. is voluntarily recalling a single lot of Daptomycin for Injection 500 mg/vial, and Daptomycin for Injection 350 mg/vial product contained in cartons imprinted with lot # R2200232 Exp: 01/2025 to the consumer/user level. This product is being recalled because Accord received… See more

#recall #drugs #unitedstates #pita #sub #ham

Recalls Accord Daptomycin for Injection - recalled due to mislabeling Durham, North Carolina, Accord Healthc... photo #1

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Recall notice

Lupin Quinapril tablets - recalled due to nitrosamine impurity, USA

3 years ago •source fda.gov • details

Lupin Pharmaceuticals Inc. is voluntarily recalling four (4) lots of Quinapril Tablets to the patient (consumer/user) level due to the presence of a nitrosamine impurity, N-Nitroso-Quinapril, observed in recent testing above the Acceptable Daily Intake (ADI) level. To date, Lupin has received no reports of illness that… See more

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

Recalls Lupin Quinapril tablets - recalled due to nitrosamine impurity Lupin Pharmaceuticals Inc. is volunta... photo #1

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Drug use, South Amherst, OH, USA

3 years ago •reported by user-bdcj8416 • details

Heavy marijuana use in the apartment beneath me

#marijuana #drugs #southamherst #ohio #unitedstates

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Recall notice

TUMS Peppermint Regular Strength tablets - recalled due to contamination, Canada

3 years ago •source recalls-rappels.canada.ca • details

GlaxoSmithKline Consumer Healthcare ULC is recalling one lot of TUMS Peppermint Regular Strength tablets after some tablets were found to contain fragments of fibreglass and other material, including paper and aluminum foil. The product is sold in a package of three rolls containing 12 tablets each, and… See more

#drugs #recall #canada #pepper #roll

Recalls TUMS Peppermint Regular Strength tablets - recalled due to contamination GlaxoSmithKline Consumer He... photo #1

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OAB Trospium Chloride 20mg, Seaside, CA, USA

3 years ago •reported by user-tzbty999 • details

Medicine for OAB Trospium Chloride 20mg - first 3 pills worked fine 4th pill not the same was like a strong diet pill kept me up all night with heart beating too fast the following days heart was still beating faster than normal - I reported the… See more

#drugs #seaside #california #unitedstates

Consumer Safety Report OAB Trospium Chloride 20mg Medicine for OAB Trospium Chloride 20mg - first 3 pills worked fine 4th p... photo #1

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Recall notice

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

3 years ago •source fda.gov • details

Exela Pharma Sciences, LLC, (Exela) is expanding their recall, adding fourteen (14) lots to the ongoing voluntary recall of forty-nine (49) lots of Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL vial, 20-count carton. A total of 63 lots are now being recalled to the consumer level.… See more

#drugs #recall #unitedstates #corn #sub

Recalls Exela Sodium Bicarbonate Injection vial - recalled due to vial breakage Exela Pharma Sciences, LLC,... photo #1

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Recall notice

Healthy Sense and People’s Choice Daily multi vitamin with Iron and Women’s daily vitamin with iron - recalled due to due to components lower than declared, USA

3 years ago •source fda.gov • details

Mason Vitamins Inc. has issued a nationwide voluntary recall of the specific lot of Healthy Sense Daily Multiple with Iron and People’s Choice Women's Daily Vitamins with Iron due to Vitamin A, Vitamin B12, Vitamin C, Vitamin E and Pantothenic Acid amounts being lower than the declared… See more

#drugs #recall #unitedstates #healthychoice #ro-tel

Recalls Healthy Sense and People’s Choice Daily multi vitamin with Iron and Women’s daily vitamin with iron... photo #1

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Recall notice

Mylan Institutional LLC Octreotide Acetate Injection - recalled due to due to glass particulates, USA

3 years ago •source fda.gov • details

Mylan Institutional LLC, a Viatris company, is voluntarily recalling lot AJ21002, exp 3/2024, of Octreotide Acetate Injection, 500 mcg/mL, packaged in a carton of ten 1mL syringes. This lot is being recalled at the user (hospital/pharmacy) level due to a product complaint of the presence of glass… See more

#blood #drugs #unitedstates #pita #sub

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Recall notice

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

3 years ago •source fda.gov • details

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 #unitedstates #sub #vegetable #meat #ro-tel

Recalls Aurobindo Pharma Quinapril and Hydrochlorothiazide Tablets - recalled due to due to presence of impu... photo #1

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Recall notice

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

3 years ago •source fda.gov • details

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 #unitedstates #corn #sub

Recalls Exela & Civica Sodium Bicarbonate Injection - recalled due to vial breakage Exela Pharma Sciences, L... photo #1

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Safety Reports: Drugs

Real Time Reports

Accord Daptomycin for Injection - recalled due to mislabeling, USA

Lupin Quinapril tablets - recalled due to nitrosamine impurity, USA

Drug use, South Amherst, OH, USA

TUMS Peppermint Regular Strength tablets - recalled due to contamination, Canada

OAB Trospium Chloride 20mg, Seaside, CA, USA

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

Healthy Sense and People’s Choice Daily multi vitamin with Iron and Women’s daily vitamin with iron - recalled due to due to components lower than declared, USA

Mylan Institutional LLC Octreotide Acetate Injection - recalled due to due to glass particulates, USA

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

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

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