Hill-Rom 100 Low Bed; Model No. P3930.
FDA device recall Z-1603-2008 · posted 2008-09-05 · Terminated
Recall details
- Recalling firm
- Hill-Rom, Inc.
- 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.
- Action taken
- 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
- Status
- Terminated
- Product code
- FNL
- Quantity affected
- 753 beds
- Distribution
- Worldwide: USA and Canada.
- Date initiated
- 2008-04-08
- Date posted
- 2008-09-05
- Date terminated
- 2010-10-13
- Location
- Batesville, IN
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