Mallinckrodt Manufacturing, LLC Recalls One-Way Valve, 22F x 22M for Not Opening Properly
The One-Way Valve, 22F x 22M is a single-use device accessory used to prevent backward flow of nitric oxide gas into the airways.
The One-Way Valve, 22F x 22M is a single-use device accessory used to prevent backward flow of nitric oxide gas into the airways.
Mon, 11 Sep 2023 13:45:03 -0400
Jemperli (dostarlimab for injection) is indicated:in combination with platinum-containing chemotherapy for the treatment of adult patients with primary advanced or recurrent mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) endometrial cancer.
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. No other Sandimmune for
Fri, 08 Sep 2023 10:23:34 -0400
FOR IMMEDIATE RELEASE – September 8, 2023 – EWING, N.J – 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)
Thu, 07 Sep 2023 08:42:32 -0400
Wed, 06 Sep 2023 16:59:34 -0400
Dans le traitement hebdomadaire du diabète de type 2 chez l'adulte, pour améliorer la régulation de la glycémie.
Tue, 05 Sep 2023 09:41:52 -0400
Jemperli (dostarlimab pour injection) est indiqué : en combinaison avec une chimiothérapie à base de sels de platine dans le traitement du cancer de l'endomètre (CE) primaire récidivant ou
à un stade avancé associé à une déficience du système de réparation des mésappariements
(SRM) ou à une instabilité microsatellitaire (IMS) élevée, chez l'adulte.
Brooklyn, New York, 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 trea
Brooklyn, New York, 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 trea
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