Healthmark Industries Co., Inc. announces that it is now offering a product called BactiQuik," a new prepackaged 1 ML vial of microbial suspensions that can be quickly and easily mixed with Artificial Test Soil (ATS) to perform validation testing for disinfection and sterilization.
The vials that they come in contain a pure population of approximately 1x108 CFU/ML. They are offered individually by either viable Geobacillus stearothermophilus or Bacillus atrophaeus. G. stearothermophilus has a known resistance for steam sterilization, and B. atrophaeus for ethylene oxide and dry heat sterilizations. When mixed with ATS or other simulated-use test soils, your reprocessing instructions from cleaning through sterilization can be validated.
Source: Healthmark Industries Co., Inc.
Getting Down and Dirty With PPE: Presentations at HSPA by Jill Holdsworth and Katie Belski
June 26th 2025In the heart of the hospital, decontamination technicians tackle one of health care’s dirtiest—and most vital—jobs. At HSPA 2025, 6 packed workshops led by experts Jill Holdsworth and Katie Belski spotlighted the crucial, often-overlooked art of PPE removal. The message was clear: proper doffing saves lives, starting with your own.
Unmasking Vaccine Myths: Dr Marschall Runge on Measles, Misinformation, and Public Health Solutions
May 29th 2025As measles cases climb across the US, discredited myths continue to undercut public trust in vaccines. In an exclusive interview with Infection Control Today, Michigan Medicine’s Marschall Runge, PhD, confronts misinformation head-on and explores how clinicians can counter it with science, empathy, and community engagement.
Silent Saboteurs: Managing Endotoxins for Sepsis-Free Sterilization
Invisible yet deadly, endotoxins evade traditional sterilization methods, posing significant risks during routine surgeries. Understanding and addressing their threat is critical for patient safety.
Endoscopes and Lumened Instruments: New Studies Highlight Persistent Contamination Risks
May 7th 2025Two new studies reveal troubling contamination in both new endoscopes and cleaned lumened surgical instruments, challenging the reliability of current reprocessing practices and manufacturer guidelines.