Surgical saw blades are medical devices used for bone shaping. They differ in size and usage according to their usage areas. Since the implant will be applied to the shaped bone, the millimeter differences in the surgical saw blades are also important. A surgical saw blade must be used in accordance with the cutting guide igaps used especially in knee arthroplasty. You can reach more detailed information from the link https://www.acf.com.tr/how-to-choose-surgical-saw-blades-where-are-they-used/ . There are risks waiting for you even when you make the right choice of the blade you bought and when your order reaches you. So what should we check in the surgical saw blades we purchased and how should we protect ourselves from risks?
When the reasons for recall of finished products are examined, it is understood that there are typographical errors in labeling and/or marking and sterilization dates. The errors encountered are grouped under 2 main headings. (You can check international recalls at links such as https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls .)
In these processes, only the persons responsible for the label may attach the labels of other party products to the marked products, causing incorrect product use. What are the risks here? Although the thickness of the surgical saw blade is not suitable for the cutting guide, there will be problems when trying to use it with the label information. If the surgical saw blade thickness is thicker than the area to be used in the guide; may not enter the guide, may be jammed, may produce heavy metal dust due to excessive friction, may become hot and prolong the surgery and/or healing process.
If the blade thickness used is thinner than the area to be used in the guide; Since it will oscillate excessively in the up and down direction, it may make it difficult for the physician to control, the expected smooth surface may not occur in the incision area, and may not allow the implanted product to be placed correctly.
Although the thickness of the surgical saw blade allows for different sizes in hip prosthesis, it must be in accordance with the cutting guide designed by the prosthesis companies in knee prosthesis incisions. Although the measurements are millimetric, each millimeter can cause faulty operation. Since the healthy use of the prosthesis for many years depends on the smoothness of the incision suitable for the prosthesis, special attention should be paid to the selection of the surgical saw blade and it should be ensured that the beginning of the operation process is correct.
Following this misrepresentation, there may be a risk of contamination with the use of products that have passed the sterile safety date. To avoid such a risk, the sterile validity period can be learned and the compatibility of the production date on the label with the sterile date can be checked.
For this reason, before the products are taken to the warehouse or in cases where the outer carton of the product does not allow to read the marking, it should be checked whether the label and marking information are compatible with each other before use. This method is a measure that significantly reduces risks.
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Product Recall; It is a voluntary withdrawal or recall from the market by the manufacturer of the device for technical and medical reasons, depending on
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Surgical Power Tool Systems are devices that complete their preparation for use by sterilising at 135 degrees due to their area of use and design.
