UNO 100 Patient Lift
FDA device recall Z-0276-06 · posted 2005-12-13 · Terminated
Recall details
- Recalling firm
- Liko, Inc.
- Reason for recall
- Incorrect length leg pin bolts may cause patient lift failures
- Action taken
- Liko Inc. initiated the recall to Distributors of the Recall on 11/14/05 via UPS. Direct customers will be notified by letter on /about 12/1/05.
- Root cause
- Other
- Status
- Terminated
- Product code
- FSA
- Quantity affected
- 548 units
- Distribution
- Nationwide
- Date initiated
- 2005-11-14
- Date posted
- 2005-12-13
- Date terminated
- 2008-02-20
- Location
- Franklin, MA
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