| 释义 |
class recall The recall of a class I, II or III FDA-regulated medical device or product, the use of or exposure to which carries a significant risk of adverse health effects or deathclass recall Regulatory affairs The recall of an FDA-regulated medical device or product, the use of or exposure to which a reasonable probability exists for adverse health effects or deathclass re·call (klas rē'kawl) A legal term that, in health care, mandates that all patients who have received a given form of implant be examined for possible malfunction of the implant. |