The Food and Drug Administration (FDA), United States, has issued a Class I recall on Nemschoff Perinatal Bassinet products with models number of BSNT/01, BSNT/02, BSNT/03 and BSNT/04.
The manufacturer of the device, Nemschoff Chairs, Inc, is correcting issues with casters, door hinges, drawer slides, and the bassinet surround of the affected devices. Besides, Nemschoff also adds labeling to the product regarding specific instructions for cleaning the bassinet tub and drawer weight limits.
According to FDA, the affected devices have been distributed in US and Canada.
For details, please refer to FDA website
http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm292057.htm
If you are in possession of the product, please contact your supplier for necessary actions.