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Safety Reports: Drugs

Updated:

Real Time Reports

Family Dollar is initiating a voluntary retail-level product recall of certain over-the-counter drugs and medical devices regulated by the U.S. Food and Drug Administration (FDA). These items were stored outside of labeled temperature requirements by Family Dollar and inadvertently shipped to certain stores on or around June… See more

#medicaldevices #drugs #recall #familydollar #unitedstates

312   Comments Comment
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 #unitedstates

312   Comments Comment
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 #unitedstates

312   Comments Comment
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

312   Comments Comment
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

312   Comments Comment
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

312   Comments Comment
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

313   Comments Comment
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

312   Comments Comment
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

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

312   Comments Comment