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4 , e2012065 (2012)

FDA noted that the correction is part of a class I recall in which users did not receive the instructions for use addendum that notifies them of the risk of decreased oxygen levels or potential lung tissue injury from overexpansion when the devices are used in the home care setting

Luger TA, et al

Furthermore, the enzyme was stable in a wide pH range (2.010.0) [112]

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