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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Purely Soothing 15% MSM Drops - recalled due to non-sterility, USA

2 years ago •source fda.gov • details

Pharmedica USA LLC is voluntarily recalling two lots of Purely Soothing, 15% MSM Drops to the consumer level. This product is being recalled due to non-sterility. To date, Pharmedica USA LLC has not received any reports of adverse events or illness related to this recalled product. Product… See more

#recall #drugs #unitedstates #ro-tel

Recalls Purely Soothing 15% MSM Drops - recalled due to non-sterility Pharmedica USA LLC is voluntarily reca... photo #1
312   Comments Comment

Recall notice

Apotex Brimonidine Tartrate Ophthalmic Solution, 0.15% - recalled due to lack of sterility, USA

2 years ago •source fda.gov • details

Apotex Corp., with the knowledge of the US FDA, is initiating a voluntary recall at the Consumer level for six (6) lots of Brimonidine Tartrate Ophthalmic Solution, 0.15% specified below. This recall is being initiated out of an abundance of caution due to cracks that have developed… See more

#recall #drugs #unitedstates #ro-tel

Recalls Apotex Brimonidine Tartrate Ophthalmic Solution, 0.15% - recalled due to lack of sterility Apotex Co... photo #1
312   Comments Comment

Recall notice

Delsam Pharma's Artificial Eye Ointment - recalled due to microbial contamination, USA

2 years ago •source fda.gov • details

Global Pharma Healthcare is voluntarily recalling Batch No. H29 of Artificial Eye Ointment, distributed by Delsam Pharma to the consumer level, due to possible microbial contamination. Additionally, some product packaging is leaking or may otherwise be compromised. The product was distributed nationwide in the United States, and… See more

#recall #drugs #unitedstates #ro-tel

Recalls Delsam Pharma’s Artificial Eye Ointment - recalled due to microbial contamination Global Pharma Heal... photo #1
312   Comments Comment

Recall notice

Snowy Range Blue Hand Sanitizer - recalled due to presence of methanol, USA

2 years ago •source fda.gov • details

nanoMaterials Discovery Corporation is voluntarily recalling all lots of its Alcohol Antiseptic 80% Alcohol Solution branded as "Snowy Range Blue" in four fluid ounce spray dispenser packaging to the consumer level. Certain batches of the company's Alcohol Antiseptic 80% Alcohol Solution may exceed FDA limits for methanol.… See more

#recall #drugs #unitedstates #sub

Recalls Snowy Range Blue Hand Sanitizer - recalled due to presence of methanol nanoMaterials Discovery Corpo... photo #1
312   Comments Comment

Recall notice

PrimeZEN Black 6000 male enhancement capsules - recalled due to undeclared ingredients, USA

2 years ago •source fda.gov • details

Volt Candy is voluntarily recalling one lot of PrimeZen Black 6000, 2000 mg capsule, to the consumer level. FDA analysis has found PrimeZen Black 6000 capsules to be tainted with sildenafil & tadalafil. Sildenafil and tadalafil are phosphodiesterase (PDE-5) inhibitors found in FDA-approved products for the treatment… See more

#blood #recall #drugs #unitedstates #sub

Recalls PrimeZEN Black 6000 male enhancement capsules - recalled due to undeclared ingredients Volt Candy is... photo #1
312   Comments Comment

Recall notice

EzriCare & Delsam Pharma Artificial Tears - recalled due to Potential microbial contamination, USA

2 years ago •source fda.gov • details

Global Pharma Healthcare is voluntarily recalling all lots within expiry of their Artificial Tears Lubricant Eye Drops, distributed by /EzriCare, LLC- and Delsam Pharma, to the consumer level, due to possible contamination. The Centers for Disease Control and Prevention (CDC) alerted FDA to an investigation of a… See more

#recall #drugs #unitedstates

Recalls EzriCare & Delsam Pharma Artificial Tears - recalled due to Potential microbial contamination Global... photo #1
312   Comments Comment

Recall notice

IBSA TIROSINT®-SOL (levothyroxine sodium) - recalled due to subpotency, USA

2 years ago •source fda.gov • details

IBSA Pharma Inc. is voluntarily recalling 27 lots of TIROSINT®-SOL (levothyroxine sodium) Oral Solution to the consumer level. This voluntary recall has been initiated because these lots may be subpotent. The company’s analyses show a slight decrease below 95.0% of its labeled amount in levothyroxine sodium (T4)… See more

#drugs #unitedstates #sub #patio

Recalls IBSA TIROSINT®-SOL (levothyroxine sodium) - recalled due to subpotency IBSA Pharma Inc. is voluntar... photo #1
312   Comments Comment

Recall notice

Banana Boat Hair & Scalp Spray SPF 30 - recalled due to the presence of benzene, USA

2 years ago •source fda.gov • details

Edgewell Personal Care Issues Voluntary Nationwide Recall of Banana Boat Hair & Scalp Sunscreen Due to the Presence of Benzene, one additional lot code ("20301CF") has been added to the recall. The modified announcement follows: Edgewell Personal Care Company (NYSE: EPC) today expanded its voluntary nationwide recall… See more

#blood #drugs #unitedstates #banana #ro-tel

Recalls Banana Boat Hair & Scalp Spray SPF 30 - recalled due to the presence of benzene Edgewell Personal Ca... photo #1
312   Comments Comment

Recall notice

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

3 years ago •source fda.gov • details

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 #unitedstates

Recalls Spectrum Epinephrine bulk API - recalled due to product discoloration Spectrum Laboratory Products,... photo #1
312   Comments Comment

Recall notice

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

3 years ago •source fda.gov • details

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 #unitedstates #pita

Recalls Hospira, Inc. Vancomycin Injection - recalled due to extraneous materials Pfizer company, is volunta... photo #1
312   Comments Comment

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