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Terminated

Hill-Rom Newborn bassinet; model P248.

FDA Recall Z-0303-04 · Posted 2004-01-08

Recalling FirmHill-Rom, Inc.
Recall StatusTerminated
Product CodeFMS
Date Initiated2003-12-19
Date Terminated2004-09-14

Reason for Recall

The caster/wheel may come off of the bassinet, causing the bassinet to tip.

Firm Action

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

Distribution Pattern

United States, Australia, Canada, China, France, Germany, Honduras, Israel, Japan, Mexico, Panama, Taiwan, Turkey, United Arab Emirates and United Kingdom.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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