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Safety Reports: Drugs

Updated: January 9, 2023 11:00 PM

Spectrum Epinephrine bulk API - recalled due to product discoloration, USA

1 year ago •source fda.gov • details

Recall notice

Spectrum Laboratory Products, Inc. is voluntarily recalling three lots of Epinephrine (L-Adrenaline) USP, a bulk active pharmaceutical ingredient (API) used to manufacture or compound prescription products, to the user level. Customer complaints have found the product to be discolored. Product was distributed directly from Spectrum facilities nationwide… See more

#blood #recall #drugs #us

Spectrum Epinephrine bulk API - recalled due to product discoloration photo #1

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Hospira, Inc. Vancomycin Injection - recalled due to extraneous materials, USA

1 year ago •source fda.gov • details

Recall notice

Pfizer company, is voluntarily recalling one lot of Vancomycin Hydrochloride Injection, USP, 1.5 g/vial Single Dose Fliptop Vial, lot 33045BA, to the user level due to two visible glass particulates observed in a single vial. The product was distributed nationwide to wholesalers/hospitals/ institutions in the United States… See more

#recall #drugs #us #pita

Hospira, Inc. Vancomycin Injection - recalled due to extraneous materials photo #1

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Accord Daptomycin for Injection - recalled due to mislabeling, USA

1 year ago •source fda.gov • details

Recall notice

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 #us #pita #sub #ham

Accord Daptomycin for Injection - recalled due to mislabeling photo #1

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Lupin Quinapril tablets - recalled due to nitrosamine impurity, USA

1 year ago •source fda.gov • details

Recall notice

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 #us #vegetable #meat #ro-tel

Lupin Quinapril tablets - recalled due to nitrosamine impurity photo #1

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Drug use, South Amherst, OH, USA

1 year ago •reported by user-bdcj8416 • details

Heavy marijuana use in the apartment beneath me

#marijuana #drugs #southamherst #ohio #us

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

1 year ago •source recalls-rappels.canada.ca • details

Recall notice

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 #ca #pepper #roll

TUMS Peppermint Regular Strength tablets - recalled due to contamination photo #1

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OAB Trospium Chloride 20mg, Seaside, CA, USA

1 year 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 #us

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

1 year ago •source fda.gov • details

Recall notice

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

#recall #drugs #us #corn #sub

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

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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

1 year ago •source fda.gov • details

Recall notice

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 #us #healthychoice #ro-tel

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 photo #1

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

1 year ago •source fda.gov • details

Recall notice

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 #us #pita #sub

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Safety Reports: Drugs

Spectrum Epinephrine bulk API - recalled due to product discoloration, USA

Hospira, Inc. Vancomycin Injection - recalled due to extraneous materials, USA

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

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