Autoclaves for BSL-3 Facilities—Part 2: Autoclave Door Safety Written by: Scott Mechler This is the second of three articles describing BSL-3 autoclaves, also commonly known as biocontainment sterilizers. These types of sterilizers are essential in handling microbes that can lead to serious or potentially lethal disease through inhalation. In this article we review the important aspects of the autoclave door design that are essential for every BSL-3 […] Tweet Like Share
Autoclaves for BSL-3 Facilities—Part 1: The Bio-Seal Written by: Scott Mechler This is the first of three articles describing BSL-3 autoclaves, also commonly known as biocontainment sterilizers. These types of sterilizers are essential in handling microbes that can lead to serious or potentially lethal disease through inhalation. In this article we explore the importance of the bio-seal, a feature that must be incorporated into a BSL-3 […] Tweet Like Share
7 Common Causes for Failure of a Bowie-Dick Test Written by: Amit Gupta Sterilization departments have one of the most important responsibilities within a healthcare facility — ensuring that all surgical instruments and other reusable equipment are sterilized and safe to use during upcoming procedures. Without these services, operations at hospitals and ambulatory surgery centers would grind to a halt. In laboratory settings (especially in ones that carry […] Tweet Like Share
CSS CEO Contributes to New ABSA Book on Sustainability Written by: Scott Mechler Our customers have come to know and trust CSS products as the most reliable, affordable and customizable autoclaves for laboratory and medical research facilities across the globe. This reputation recently led to Consolidated lending a helping hand to The American Biological Safety Association (ABSA). Arthur Trapotsis, President and CEO of Consolidated Sterilizer Systems, helped co-author […] Tweet Like Share
How To Calibrate Your Autoclave (Includes 11 Step Sample Procedure) Written by: Scott Mechler “Calibration” is a word that is frequently used in the steam sterilization industry. This blog post will explore what it is, what is involved in doing it right, alternatives, and the potential effects on an existing sterilization process. What is Calibration? At its very basic premise, calibration is bringing the response of a sensor (e.g. […] Tweet Like Share
Biosafety Levels 1, 2, 3 & 4: What’s the Difference? Written by: Arthur Trapotsis Updated 11/3/22: Information about the biosafety level requirements for handling SAR-CoV-2 (COVID-19 coronavirus) can be found here. Safety is of the utmost importance in any laboratory setting, especially when working with autoclaving equipment. In order to ensure the safety of lab personnel, the environment and surrounding communities, the Centers for Disease Control and Prevention (CDC) […] Tweet Like Share
Laboratory Autoclave Steam Sterilization Cycles, Part 10: Immediate-Use (Flash) Sterilization Cycle Written by: Arthur Trapotsis There has been much debate around the antiquated term “flash sterilization.” A concerted effort has been made by the Association for Advancement of Medical Instrumentation (AAMI), the Joint Commission (JC) and the Food and Drug Administration (FDA), to clarify the use of flash sterilization, which these organizations now refer to as “immediate use” sterilization. This sterilization cycle is not intended for routine instrument sterilization but only when specific instruments are needed for an emergency procedure. Read more → Tweet Like Share
Why To Autoclave Liquids With a Load Probe Written by: Amit Gupta In our previous Sterilization Cycles post on the F0 Cycle, we briefly reviewed the process for autoclaving liquids with a load probe. This post further discusses the benefits of using a load probe for sterilization validation. A load probe is a temperature sensing probe located inside the laboratory’s autoclave chamber. It is configured such that […] Tweet Like Share
Laboratory Autoclave Steam Sterilization Cycles, Part 9: Air Over-Pressure Cycle Written by: Arthur Trapotsis In the ninth installment of our Steam Sterilization Cycles Series, we explore Air Over–Pressure, another cycle used to sterilize a specific type of liquid load. An Air Over-Pressure Cycle is used to sterilize small liquid loads that are extremely sensitive to evaporation or boil-over in laboratory autoclaves. Typical applications for this cycle include pre-filled pipet tips, small pre-filled vials, loosely capped flasks, foil sealed glassware, or any partially vented containers where even small amounts of evaporation are not acceptable. Read more → Tweet Like Share
Bowie-Dick & Vacuum Leak Tests: Autoclave Sterilization Cycles Written by: Arthur Trapotsis The entire purpose of a laboratory or medical autoclave is to, quite simply, sterilize; however, without the proper conditions for sterility, an autoclave may fall short of its mission. Validation is an essential quality assurance measure designed to ensure that your autoclave operates exactly as intended. There are a number of different ways to validate […] Tweet Like Share
7.12.23 Cordyceps Sterilization: How to Kill “The Last of Us” Parasite → In HBO’s recent adaptation of “The Last of Us,” a popular action-adventure video game, life as we know it is upended by a parasitic fungus that transforms its human hosts into zombies. The culprit? Cordyceps, a real-life genus of fungus which is best known for infecting insects (most famously ants) in much the same manner […]
6.30.23 Top 13 Sterile Processing Mistakes in Hospitals → When it comes to ensuring patient safety in hospitals and ambulatory surgery centers (ASCs), the Sterile Processing Department (SPD) is among the last lines of defense. It’s this department’s sole responsibility to make sure that reusable instruments and devices are properly decontaminated, sterilized, and ultimately safe to use in future procedures — protecting patients from […]
6.22.23 Sterilization vs. High-Level and Low-Level Disinfection [a 3-Point Comparison] → In a 1939 paper, microbiologist Earle H. Spaulding introduced a system for determining which medical devices and instruments needed disinfection and which ones required sterilization. In it, he proposed that critical instruments would need to be subjected to more stringent disinfection protocols than non-critical patient care items. Today, this framework is fittingly known as Spaulding […]
