Learn SPD · Decontamination

Decontamination is where used medical devices begin their journey back toward safe use.

It is a controlled process designed to reduce contamination, protect personnel, and prepare reusable devices for the steps that follow.

Before You can Make it Safe, You have to make it clean.

An illustration of a person cleaning surgical instruments in a sterilization process, with a step-by-step guide. The steps include receiving contaminated instruments, sorting, cleaning, rinsing, drying, and verifying. The person is wearing protective gear including a face mask, face shield, gloves, and a gown, working at an industrial sink in a sterile medical environment.

The Purpose of Decontamination

This isn’t just the “dirty side.”

Decontamination is the beginning of a controlled reprocessing system.

Devices arrive contaminated from patient care. The work performed here reduces contamination and prepares those devices to move safely and effectively through the rest of the process.

RECEIVE → PREPARE → CLEAN → RINSE → DRY → VERIFY

Every step affects the next one.

POOR CLEANING CANNOT BE FIXED BY STERILIZATION.

An infographic titled 'The Decontamination Path' illustrating six steps in decontaminating surgical instruments. Step 1: Receive, showing a worker handling used instruments in a tray. Step 2: Prepare, worker disassembling instruments. Step 3: Clean, using brushes and water. Step 4: Rinse, under a water faucet. Step 5: Dry, wiping instruments with a cloth. Step 6: Verify, inspecting instruments under a light. The infographic emphasizes safe device handling for better outcomes.

Personnel Safety

The First Thing You Protect Is You.

Contaminated devices can expose personnel to blood, body fluids, chemicals, sharps, aerosols, and other hazards.

Appropriate personal protective equipment creates a barrier between the worker and those hazards.

Depending on the task and facility requirements, decontamination PPE may include:

Head Covering

Face + eye Protection

Gloves

Fluid-Resistant Protection

Foot or Shoe Protection

PPE must be appropriate for the hazards of the work being performed.

Safety starts before the first instrument is touched.

An illustration of a person wearing protective gear in a clean industrial environment. The person is dressed in a blue head covering, face mask, safety glasses, disposable gown, gloves, slip-resistant shoes, and an apron. The image highlights various safety gear, including head covering, face mask, eye protection, fluid-resistant gown, gloves, and foot protection, with labels and descriptions for each. There is a sign on the wall emphasizing decontamination and cleaning procedures.

Dirty moves toward clean. Not Back Again.

Sterile processing workflow is designed to reduce the risk of cross-contamination.

Contaminated devices enter the decontamination area.

Cleaning occurs.

Devices that have completed the required decontamination process move forward toward inspection, preparation, packaging, and sterilization.

Contaminated → Cleaned → Prepared → Sterilized

The process should move in one direction.

DON’T LET THE WORKFLOW WORK BACKWARD.

Infographic illustrating a one-way workflow process for medical device sterilization, starting from contaminated used instruments, through decontamination, inspection and preparation, sterilization, and storage and distribution, emphasizing safety and risk reduction at each stage.

Workflow

Point-of-Use Treatment

Cleaning Doesn’t Begin At the Sink.

What happens immediately after a device is used can affect what happens later in decontamination.

Point-of-use treatment helps prevent soil from drying and supports effective cleaning later.

Devices should be prepared and transported according to the applicable manufacturer’s instructions and facility procedures.

Don’t give soil time to become a bigger problem.

Point-of-use treatment supports decontamination.

It does not replace it.

Transport

Contain the Contamination.

Used devices must travel from the point of use to the decontamination area without unnecessarily exposing personnel, patients, or the environment to contamination.

Safe transport considers:

CONTAINMENT

LEAKAGE

SHARPS

DEVICE PROTECTION

IDENTIFICATION

FACILITY WORKFLOW

cONTAMINATED DEVICES SHOULD ARRIVE CONTAINED, CONTROLLED, AND READY FOR PROCESSING.

A safety poster about properly containing contamination during a medical procedure. It contrasts correct practices, like transporting contaminated instruments in a closed, labeled container, with improper practices, like leaving contaminated instruments exposed. The poster emphasizes controlling contamination to protect people and ensure a safe environment.

Preparation for cleaning

Before cleaning begins, devices must be prepared according to their instructions.

That may require:

OPENING

DISASSEMBLING

UNLOCKING

REMOVING COMPONENTS

ACCESSING INTERNAL CHANNELS

POSITIONING FOR CLEANING

Complex devices may require specific steps before their surfaces can actually be reached.

You Can’t Clean What You Can’t Reach.

Access comes before cleaning.

An infographic illustrating the process of cleaning medical devices. It emphasizes opening the device, disassembling it, and exposing internal parts for thorough cleaning. The infographic features sections for opening, disassembling, and exposing devices, with corresponding example images of medical tools like forceps, scissors, a spray gun, and an arthroscopic cannula. It also includes tips about device preparation, following manufacturer instructions, and maintaining proper cleaning standards.

Device-Specific Processing

Memory Is Not A Cleaning Instruction.

Reusable devices can differ dramatically in their cleaning requirements.

The manufacturer’s instructions may specify:

  • disassembly

  • water requirements

  • detergent type or concentration

  • temperature

  • brushing or flushing

  • immersion restrictions

  • cleaning equipment

  • rinse requirements

  • drying requirements

  • inspection or verification steps

The Device Determines the Process.

When requirements need to be confirmed, use the current applicable instructions rather than memory or habit.


Related 5-Minute Huddle

Memory Is Not the IFU

When a requirement matters, verify it using the current applicable source rather than relying on memory or “how we’ve always done it.”

Detergents + Cleaning Solutions

The Chemistry Has a Job.

Cleaning solutions help loosen, suspend, dissolve, or remove soils so they can be separated from device surfaces.

Effective use depends on following the applicable requirements for things such as:

CORRECT PRODUCT

CORRECT CONCENTRATION

CORRECT WATER CONDITIONS

CORRECT TEMPERATURE

CORRECT CONTACT TIME

More detergent is not automatically better.

Hotter water is not automatically better.

Longer exposure is not automatically better.

Follow the process.

Don’t improvise the chemistry.

Infographic explaining the variables in cleaning chemistry: water quality, temperature, product, concentration, and time, with an image of a detergent bottle at the center and icons representing each variable.

Manual Cleaning

Friction Does The Work.

Manual cleaning uses physical action and appropriate cleaning chemistry to remove contamination from device surfaces.

Depending on the device and its instructions, this may include:

BRUSHING

WIPING

FLUSHING

IMMERSION

IRRIGATION

OTHER DEVICE-SPECIFIC ACTIONS

Cleaning tools should be appropriate for the device and surface being cleaned.

Internal channels require attention just like external surfaces.

If the cleaning action can’t reach the soil, the soil has a place to stay.

An informational infographic demonstrating the steps to reach the soil for cleaning medical instruments. It shows parts like the external surface, internal lumen, hinge/box lock, and serrations, with descriptions of how to clean each. There are icons and text emphasizing knowing your device, using the right tools, following recommended methods, and ensuring safety for effective cleaning.

Lumens + Complex Devices

The Outside Isn’t the Whole Device.

Cannulated and complex devices contain internal surfaces that may not be visible during routine handling.

Cleaning may require specific:

  • brushes

  • flushing volumes or techniques

  • adapters

  • syringes or irrigation devices

  • mechanical cleaning connections

  • inspection methods

The exact process depends on the device manufacturer’s instructions.

Out of sight doesn’t mean out of the process.

Diagram showing how soil can hide inside a device, with external, internal, and clean lumen sections, explaining how flushing or irrigation helps remove soil from internal channels for cleaning, emphasizing that soil can remain inside even when the exterior appears clean.

Mechanical Cleaning

Machines support the Process. They Don’t Replace It.

Mechanical cleaning equipment can provide controlled, repeatable cleaning action when devices are properly prepared and loaded.

Common systems include:

Ultrasonic Cleaners

Use cavitation to help remove soil from accessible surfaces.

Washer-Disinfectors

Use programmed cycles, cleaning chemistry, water, temperature, and mechanical action.

But equipment can only work effectively when the device is compatible, correctly prepared, and properly positioned.

The machine can only clean what the process allows it to reach.

Rinsing

Cleaning chemistry has to leave, too.

After cleaning, required rinsing helps remove loosened soil and cleaning solution residues from device surfaces.

Rinsing requirements may depend on:

THE DEVICE

THE CLEANING AGENT

WATER QUALITY

THE CLEANING METHOD

MANUFACTURER INSTRUCTIONS

cLEANING ISN’T COMPLETE JUST BECAUSE THE SCRUBBING STOPPED.

dRYING

wATER LEFT BEHIND ISN’T A FINISHING TOUCH.

Devices should be dried according to applicable instructions before they continue through reprocessing.

Pay attention to:

EXTERNAL SURFACES

HINGES + JOINTS

RECESSES

LUMENS

OTHER INTERNAL AREAS

Complex devices may require specific drying methods.

Don’t forget the places you can’t easily see.

An infographic explaining where water hides in medical instruments like scissors. Shows parts including hinge/box lock, internal lumen, and recessed areas, with instructions for finding and removing water to prevent damage and contamination.

Cleaning Verification

“I Cleaned It” Isn’t the same as “It’s Clean.”

The cleaning process should produce a device that meets the requirements to move forward.

Verification may involve:

VISUAL INSPECTION

ADEQUATE LIGHTING

MAGNIFICATION

INTERNAL INSPECTION

DEVICE-SPECIFIC TESTING

PROCESS OR EQUIPMENT MONITORING

The appropriate verification method depends on the device, process, equipment, and applicable requirements.

Cleaning is a process. Verification checks the result.

Comparison of cleaned versus verified medical device cleaning process, showing a surgical instrument on a sterilization tray for cleaned and a gloved hand inspecting a device under a light for verified.

The Decision Point

Don’t send the problem forward.

You find:

VISIBLE SOIL.

RESIDUE IN A HINGE.

DEBRIS INSIDE A LUMEN.

A QUESTIONABLE INTERNAL SURFACE.

A DEVICE THAT WASN’T DISASSEMBLED CORRECTLY.

AN UNRESOLVED CLEANING CONCERN.

The answer isn’t:

“Sterilization will take care of it.”

STOP THE PROCESS.

Address the cleaning concern according the applicable instructions and facility procedures before the device continues.

Sterilization is not a substitute for cleaning.

Reality Check

The fastest path forward may be backward.

An instrument reaches inspection and visible residue is discovered inside a joint.

Sending it forward would save time.

Returning it to decontamination means rework and may delay the tray.

But the process has already answered the question.

THE DEVICE ISN’T READY.

Returning it for appropriate recleaning isn’t unnecessary work.

It is the quality system doing what it is supposed to do.

Code Breaker

When the device isn’t clean, start there.

Certification questions may surround a cleaning problem with distracting details:

  • The case is waiting.

  • The instrument is needed quickly.

  • The sterilizer is ready.

  • The department is busy.

  • A coworker says it is probably fine.

Strip those details away.

WHAT IS THE SAFETY-CRITICAL PROBLEM?

If the device has not been adequately cleaned, protect the process before protecting the schedule.

Take This With You

Don’t Ask Only: “Did We Wash It?”

Ask: “Did the cleaning process actually reach and remove the contamination?

PROTECT yourself.

CONTAIN contamination.

PREPARE the device.

CLEAN every required surface.

RINSE appropriately.

DRY completely.

VERIFY the result.

A circular infographic detailing the RIE cleaning process, including steps to protect, prepare, clean, rinse, dry, verify, and finally protect again.

Continue the Process

Cleaning opens the door to everything that follows.

Once a device has been appropriately cleaned, rinsed, dried, and verified, it can move toward the next stages of reprocessing.

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