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alcon-laboratories-issues-voluntary-nationwide-recall-of-one-(1)-lot-of-systane-lubricant-eye-drops-ultra-pf,-single-vials-on-the-go,-25-count-(lot-10101),-due-to-fungal-contamination FDA
  • December 23, 2024

Alcon Laboratories Issues Voluntary Nationwide Recall of One (1) Lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101), Due to Fungal Contamination

Fort Worth, Texas. Alcon Laboratories is voluntarily recalling one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials…
Drug Test
  • December 21, 2024

Doping Control Analysis of Methylsulfonylmethane in Horses

This paper describes the administration study of MSM in two geldings following a dose of one scoop (~15 g) of Pure…
lidl-recalls-taste-of-deutschland-buttered-vegetables-due-to-undeclared-milk-allergens FDA
  • December 20, 2024

Lidl Recalls Taste of Deutschland Buttered Vegetables Due to Undeclared Milk Allergens

DECEMBER 20, 2024 – Lidl US is recalling all lots of their Taste of Deutschland Buttered Vegetables 10.5 oz box…
recall-of-jose-madrid-salsa-chipotle-con-queso 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…
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 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…
early-alert:-nephroscope-sheath-issue-from-trokamed-gmbh 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
endo-usa,-inc.-issues-voluntary,-nationwide-recall-of-adrenalin-chloride-solution-(epinephrine-nasal-solution,-usp)-due-to-the-potential-for-administration-errors 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…
orgain-issues-voluntary-allergy-alert-on-possible-undeclared-peanut-residue-in-a-single-batch-of-30g-protein-organic-plant-based-powder-–-chocolate-2.01lb 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…