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: Illinois Injury Lawyer BlogFDA recalls defective baby breathing monitors
The FDA gave the SmartMonitor 2 Infant Apnea Monitor a potential defective product risk on the federal Class I recall list. A Class I recall is the highest and most serious recall a defective product can be labeled in U.S., which means that the product has a reasonable probability of causing serious injury or death.
To read more about the defective product recall.
Full post as published by Illinois Injury Lawyer Blog on May 26, 2009 (boomark / email).
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