Atlas FDA

Hill-Rom Newborn bassinet; model P248.

FDA device recall Z-0303-04 · posted 2004-01-08 · Terminated

Recall details

Recalling firm
Hill-Rom, Inc.
Reason for recall
The caster/wheel may come off of the bassinet, causing the bassinet to tip.
Action taken
Recall letters dated December 19, 2003 were sent to each customer. Customers were instructed to verify the security of the casters to the base, and to visually check for loose or missing caster screws until Hill-Rom can visit each facility and perform a fix.
Root cause
Other
Status
Terminated
Product code
FMS
Distribution
United States, Australia, Canada, China, France, Germany, Honduras, Israel, Japan, Mexico, Panama, Taiwan, Turkey, United Arab Emirates and United Kingdom.
Date initiated
2003-12-19
Date posted
2004-01-08
Date terminated
2004-09-14
Location
Batesville, IN

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