Nota Informativa Importante su XELJANZ® (tofacitinib)
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Angiographic Guidewire Component is a guidewire to help place catheters into the vasculature.
Teva Pharmaceuticals has initiated a voluntary recall of lot 31328962B of Topotecan Injection 4 mg/4 mL (1 mg/mL), to the retail/institutional level in the United States. This voluntary recall was initiated based on a complaint received from a pharmacy after a single glass particle was observed ins
The LeadCare tests are used to detect blood lead level but has risk of falsely low results.
Santo Domingo, Dominican Republic – Ardil Comercial is voluntarily recalling one lot of Limar Hand Sanitizer, packaged in 4 oz bottles to the consumer level. The hand sanitizer is being recalled because it is packaged in containers that resemble water bottles. The product poses a risk of ingestion
Wed, 30 Jun 2021 15:56:12 -0400
Wed, 30 Jun 2021 11:32:09 -0400
The recall is due to issues with PE-PUR foam, used to reduce sound and vibration, breaking down and potentially entering the device’s air pathway.
The FDA revoked the emergency use authorizations for non-NIOSH-approved disposable respirators and the EUAs for decontamination and bioburden reduction systems.
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