Email
weborders@prabadincorp.com
Call us
+1 (786)-332-3938
Home
Blog
Life style
Product Catalog
X
FDA
December 20, 2024
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…
FDA
December 20, 2024
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…
FDA
December 20, 2024
Early Alert: Nephroscope Sheath Issue from Trokamed GmbH
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
FDA
December 20, 2024
Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With Plum 360, A+, and A+3 Infusion Systems Due to Reports of Allegedly Counterfeit, Untested Batteries In Use
Some CSB batteries intended for use with Plum 360, A+ or A+3 infusion pumps may be counterfeit and are not…
FDA
December 19, 2024
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…
Drug Test
December 19, 2024
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…
Drug Test
December 19, 2024
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…
FDA
December 18, 2024
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.
FDA
December 18, 2024
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.
FDA
December 18, 2024
Update: Do Not Use BioZorb Marker Implantable Radiographic Marker Devices: FDA Safety Communication
The FDA’s updated information about BioZorb Marker.
1
...
276
277
278
279
280
...
283