Arthroscopy Device Market - Restraints
One of the factors restraining growth of the arthroscopy devices market is the increasing number of FDA recalls due to product failures, component inconsistency or compromised sterility issues. For instance, in October 2014, the U.S. FDA recalled 'Shoulder Arthroscopy Pack' manufactured by Customed, Inc. because of significantly damaged sterility and packaging. Serious deficiencies in manufacturing processes, and uncontrolled and inadequate storage conditions increase risk of contamination and may result in patient infection. Thus, manufacturing issues or product failures are expected to hamper growth of the arthroscopy devices market.
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