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Drug Test
  • December 23, 2024

Detection of Oral Testosterone Undecanoate Administration in UGT2B17 del/del and del/ins Individuals. Part I: Urinary Steroid Profile and IRMS Markers

Results obtained in the present study support that the ratio 5αAdiol/E should be considered as primary marker in the ABP.…
early-alert:-endoscope-accessories-forceps/irrigation-plug-issue-from-olympus FDA
  • December 23, 2024

Early Alert: Endoscope Accessories Forceps/Irrigation Plug Issue from Olympus

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
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…
flying Healthcare
  • December 20, 2024

Flying

 Last year I wanted to gift myself with some flying lessons.  I finally managed to do that earlier this month,…
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…