Recall of Jose Madrid Salsa Chipotle Con Queso

Jose Madrid Salsa is announcing a voluntary recall of our Chipotle Con Queso Salsa. The salsa is being recalled because…

Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution (EPINEPHrine Nasal Solution, USP) Due to the Potential for Administration Errors

Endo, Inc (OTCQX: NDOI) (“Endo”), announced today that one of its operating subsidiaries, Endo USA, Inc., is voluntarily recalling all…

Early Alert: Nephroscope Sheath Issue from Trokamed GmbH

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program

Orgain Issues Voluntary Allergy Alert on Possible Undeclared Peanut Residue in a Single Batch of 30G Protein Organic Plant Based Powder – Chocolate 2.01lb

Orgain of Irvine, California is voluntarily recalling a single batch of its 30g Protein Organic Plant Based Powder – Chocolate…

The Emergence of a Novel Synthetic Nicotine Analog 6‐Methyl Nicotine (6‐MN) in Proclaimed Tobacco‐ and Nicotine‐Free Pouches Available in Europe

At the beginning of 2024, self-proclaimed tobacco- and nicotine-free pouches became available on the European market. Upon chemical analysis of…

Further Investigation Into an Environmental Source for Aminorex

The results provide evidence that resedine is an intermediary compound between barbarin and aminorex in horses and that resedine can…

Hologic, Inc. Recalls BioZorb Marker Due to Complications with Implanted Devices

Hologic, Inc. is recalling BioZorb Marker due to complications and adverse events with implanted devices.

Catheter Correction: Boston Scientific Updates Use Instructions for POLARx and POLARx FIT Cryoablation Balloon Catheters due to Higher than Anticipated Number of Reports of Atrio-Esophageal Fistula

POLARx Cryoablation Balloon Catheters treat atrial fibrillation. After reports of atrio-esophageal fistula, the use instructions are being updated.

Update: Do Not Use BioZorb Marker Implantable Radiographic Marker Devices: FDA Safety Communication

The FDA’s updated information about BioZorb Marker.