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Safety Reports: Drugs

Updated:

Ascend Laboratories Dabigatran Etexilate Capsules - recalled due to Detection of N-Nitrosodimethylamine Impurity, USA

1 year ago •source fda.gov • details

Recall notice

Ascend Laboratories LLC. is voluntarily recalling Dabigatran Etcxilate Capsules. USP 75 mg and 150 mg to the consumer/user level due to the presence of a nitrosamine. N-nitroso-dabigatran, above the established Acceptable Daily Intake (ADI) level. The product lots were distributed nationwide to wholesalers, Distributors and Retailers (dispensers)… See more

#blood #drugs #us

Ascend Laboratories Dabigatran Etexilate Capsules - recalled due to Detection of N-Nitrosodimethylamine Impurity photo #1
321

Dr Rima Recommends Nano Silver dietary supplement - recalled due to unsubstantiated health claims, USA

1 year ago •source fda.gov • details

Recall notice

CUSTOMERS OF NATURAL SOLUTIONS FOUNDATION (the “Foundation”) This is to inform you of a voluntary product recall involving the following Foundation product (the “Product”) “DR. RIMA RECOMMENDS NANO SILVER 10 PPM” The Product label is depicted for your reference and ease in identifying the Product. This recall… See more

#drugs #recall #us #sub #ro-tel

Dr Rima Recommends Nano Silver dietary supplement - recalled due to unsubstantiated health claims photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us #ro-tel

Purely Soothing 15% MSM Drops - recalled due to non-sterility photo #1
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Apotex Brimonidine Tartrate Ophthalmic Solution, 0.15% - recalled due to lack of sterility, USA

1 year ago •source fda.gov • details

Recall notice

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 #us #ro-tel

Apotex Brimonidine Tartrate Ophthalmic Solution, 0.15% - recalled due to lack of sterility photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us #ro-tel

Delsam Pharma’s Artificial Eye Ointment - recalled due to microbial contamination photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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

#drugs #recall #us #sub

Snowy Range Blue Hand Sanitizer - recalled due to presence of methanol photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us #sub

PrimeZEN Black 6000 male enhancement capsules - recalled due to undeclared ingredients photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us

EzriCare & Delsam Pharma Artificial Tears - recalled due to Potential microbial contamination photo #1
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IBSA TIROSINT®-SOL (levothyroxine sodium) - recalled due to subpotency, USA

1 year ago •source fda.gov • details

Recall notice

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 #us #sub #patio

IBSA TIROSINT®-SOL (levothyroxine sodium) - recalled due to subpotency photo #1
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Banana Boat Hair & Scalp Spray SPF 30 - recalled due to the presence of benzene, USA

1 year ago •source fda.gov • details

Recall notice

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 #us #banana #ro-tel

Banana Boat Hair & Scalp Spray SPF 30 - recalled due to the presence of benzene photo #1
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