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Safety Reports: Drugs

Updated:

KVK-Tech Betaxolol Tablets, USP - recalled due to Potential Presence of Oxycodone HCl tablet, USA

8 months ago •source fda.gov • details

Recall notice

KVK-Tech, Inc. is voluntarily recalling one lot (Batch Number: 17853A; “the batch”) of Betaxolol Tablets, USP 10 mg, White, Round, film coated biconvex tablets, debossed “K” above bisect “13” on one side and plain on the other side” to the consumer level. The batch was distributed nationwide… See more

#recall #drugs #us

KVK-Tech Betaxolol Tablets, USP - recalled due to Potential Presence of Oxycodone HCl tablet photo #1
321

Hospira Sodium Bicarbonate & Lidocaine HCl Injections - recalled due to potential presence of glass particulate matter, USA

8 months ago •source fda.gov • details

Recall notice

Hospira, Inc., a Pfizer company, is voluntarily recalling 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10mL vial; 1% Lidocaine HCl Injection, USP, 50 mg/5mL vial; and 2% Lidocaine HCl Injection, USP, 100 mg/5mL vial to the user level due to the potential presence of glass particulate matter. To… See more

#blood #recall #drugs #us

Hospira Sodium Bicarbonate & Lidocaine HCl Injections - recalled due to potential presence of glass particulate matter photo #1
321

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

8 months 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 #us

Ion & Restore brands Nasal Sprays - recalled due to due to Microbial Contamination photo #1
321

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

8 months 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 #us

Merck Animal Health Banamine/Banamine-S Update - recalled due to presence of particulate matter photo #1
321

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

8 months 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

#drugs #recall #us

BREXAFEMME® Antifungal oral medication - recalled due to Potential cross contamination photo #1
321

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

9 months 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 #us #bacilluscereus

VistaPharm Sucralfate Oral Suspension 1g/10mL - recalled due to Potential Bacillus cereus photo #1
322

Novartis Sandimunne Oral Solution - recalled due to crystallization, USA

9 months 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 #us

Novartis Sandimunne Oral Solution - recalled due to crystallization photo #1
321
F

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

9 months ago •reported by user-fhxtx618 • 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 #us

184

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

9 months 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 #us

TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to microbial contamination photo #1
321

WEFUN Capsules - recalled due to Undeclared Sildenafil, USA

9 months 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 #us

WEFUN Capsules - recalled due to Undeclared Sildenafil photo #1
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