UNO 100 EM/EE Patient Lift
FDA device recall Z-0876-05 · posted 2005-06-08 · Terminated
Recall details
- Recalling firm
- Liko, Inc.
- Reason for recall
- Incorrect length support screws may cause patient lift failure
- Action taken
- Liko notified Peridot Group by letter dated 9/29/04 of the recall. All Canadian distributors, including Peridot, will contact and inspect and replace bolts at user sites.
- Root cause
- Other
- Status
- Terminated
- Product code
- FNG
- Quantity affected
- 398 units
- Distribution
- Canada
- Date initiated
- 2004-09-24
- Date posted
- 2005-06-08
- Date terminated
- 2007-06-20
- Location
- Franklin, MA
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