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Safety Reports: Drugs

Updated: October 2, 2023 3:01 PM

Ion & Restore brands Nasal Sprays - recalled due to due to Microbial Contamination, USA

1 year ago •source fda.gov • details

Recall notice

Biomic Sciences is voluntarily recalling all lots of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray products to the consumer level. FDA testing found the product to contain microbial contamination identified as Microbacterium sp., Fictibacillus sp., Bacillus sp., (primarily B. malikii), and Paenibacillus sp (these… See more

#recall #drugs #unitedstates

Ion & Restore brands Nasal Sprays - recalled due to due to Microbial Contamination photo #1

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Merck Animal Health Banamine/Banamine-S Update - recalled due to presence of particulate matter, USA

1 year ago •source fda.gov • details

Recall notice

Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., Rahway, N.J., USA (NYSE:MRK), is voluntarily recalling 4 additional batches of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for… See more

#drugs #recall #unitedstates

Merck Animal Health Banamine/Banamine-S Update - recalled due to presence of particulate matter photo #1

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BREXAFEMME® Antifungal oral medication - recalled due to Potential cross contamination, USA

1 year ago •source fda.gov • details

Recall notice

SCYNEXIS, Inc. is conducting a voluntary nationwide recall of 2 lots of BREXAFEMME® (ibrexafungerp tablets) to the consumer level in the US market due to potential cross contamination with a non- antibacterial ß-lactam drug substance in the ibrexafungerp citrate used to manufacture the BREXAFEMME® tablets. During a… See more

#recall #drugs #unitedstates

BREXAFEMME® Antifungal oral medication - recalled due to Potential cross contamination photo #1

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VistaPharm Sucralfate Oral Suspension 1g/10mL - recalled due to Potential Bacillus cereus, USA

1 year ago •source fda.gov • details

Recall notice

VistaPharm LLC is voluntarily recalling one (1) lot of Sucralfate Oral Suspension, 1g/10mL, to the consumer level, due to Bacillus cereus contamination in the product. This product was distributed Nationwide to three (3) distributors by wholesale. To date, VistaPharm LLC has not received any reports of adverse… See more

#drugs #unitedstates #bacilluscereus

VistaPharm Sucralfate Oral Suspension 1g/10mL - recalled due to Potential Bacillus cereus photo #1

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Novartis Sandimunne Oral Solution - recalled due to crystallization, USA

1 year ago •source fda.gov • details

Recall notice

Novartis is conducting a voluntary nationwide recall at the consumer level of one lot of its Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL in the US due to crystal formation observed in some bottles, which could potentially result in incorrect dosing. This lot was distributed… See more

#recall #drugs #unitedstates

Novartis Sandimunne Oral Solution - recalled due to crystallization photo #1

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Staff and medical procedures are off way off, Lees Summit, MO, USA

1 year ago • details

My gf came here due too a some one drugging her. Then the hospital does the same thing with anxiety medicine too force their claim that she need's too be admitted she was knocked out cold for 3 days some thing needs too be done also when… See more

#drugs #leessummit #missouri #unitedstates

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TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to Microbial Contamination, USA

1 year ago •source fda.gov • details

Recall notice

Church & Dwight Co., Inc. (NYSE:CHD) today initiated a voluntary recall of one specific lot of TheraBreath Kids Strawberry Splash 16oz after the Company identified a microbial contamination due to the presence of yeast (Candida Parapsilosis) in lot #PA3083011 of the product, sold exclusively on Amazon between… See more

#recall #drugs #unitedstates

TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to microbial contamination photo #1

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WEFUN Capsules - recalled due to Undeclared Sildenafil, USA

1 year ago •source fda.gov • details

Recall notice

Hua Da Trading Inc dba Wefun Inc. is voluntarily recalling 300 Boxes of WEFUN Capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) inhibitor found in FDA-approved products for the… See more

#drugs #recall #unitedstates

WEFUN Capsules - recalled due to Undeclared Sildenafil photo #1

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Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up, USA

1 year ago •source fda.gov • details

Recall notice

Marlex Pharmaceuticals, Inc. is voluntarily recalling one lot of Digoxin Tablets USP, 0.125mg and one lot of Digoxin Tablets USP, 0.25mg to the consumer level due to Label Mix-Up. Bottles of Digoxin Tablets, USP 0.125mg s are incorrectly labeled and contain Digoxin Tablets USP, 0.25mg Tablets. Bottles… See more

#recall #drugs #unitedstates

Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up photo #1

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Dr. Berne’s MSM drops and Mist - recalled due to Bacterial & Fungal Contamination, USA

1 year ago •source fda.gov • details

Recall notice

Dr. Berne’s Whole Health Products is voluntarily recalling all lots of MSM DROPS 5%,15% Solution, Dr. Berne’s Organic Castor Oil Eye Drops and Dr. Berne’s MSM MIST 15% Solution to the consumer level. FDA analysis has found one lot (lot 6786) of Dr. Berne's MSM DROPS 5%… See more

#recall #drugs #unitedstates