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Terminated

Hill-Rom 100 Low Bed; Model No. P3930.

FDA Recall Z-1603-2008 · Posted 2008-09-05

Recalling FirmHill-Rom, Inc.
Recall StatusTerminated
Product CodeFNL
Date Initiated2008-04-08
Date Terminated2010-10-13
Product Quantity753 beds

Reason for Recall

The upper deck may collapse to its lowest position and the caster brakes may fracture if the bed is moved while the brakes are locked.

Firm Action

Consignees were notified via letter dated April 8, 2008 to lower these beds to their lowest position, to remove the beds from use if they move more than 1/2 inch with the brakes locked and that the firm will repair these beds when fixes become available. If you have questions regarding this recall, contact Hill-Rom Technical Support at 800-445-3730.

Root Cause

Device Design

Distribution Pattern

Worldwide: USA and Canada.

Official Source

View FDA Recall →

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

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