Sterile X-Ray Detectable Lap Sponges Market Restraint
Product recalls due to failure in meeting sterile conditions is expected to hamper growth of the sterile X-ray detectable lap sponges market. For instance, in March 2016, the U.S Food and Drug Administration (USFDA) recalled Kerlix X-Ray Detectable Laparotomy Sponges, Tray Pack, 16" x 17" of Covidien LLC, due to failures in sterility of the product at package seal, which may result in a potentially increased risk of infection.
Sterile X-Ray Detectable Lap Sponges Market Driver
Increasing awareness regarding use of sterile X-ray detectable lap sponges to reduce medical errors is expected to drive growth of the sterile X-ray detectable lap sponges market. For instance, according to an article published in the International Journal of Surgery and Medicine 2017, forgotten or missed foreign bodies, such as cotton sponges, gauze or instruments, after any surgical procedures may result into serious complications such as secondary infections, and tissue damage. To prevent such complication, surgical sponges with radioactive gauzes and filaments such as X-ray are routinely used after surgery.
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