Liko, Inc. began a recall of Sabina I and II EM/EE Patient Lift on . The reason FDA records is "Incorrect length support screws may cause patient lift failure". As of , the recall status on record is Terminated.
Recall record
- Recall number
- Z-0877-05
- Status
- Terminated
- Initiated
- Posted
- Terminated
- Recalling firm
- Liko, Inc.
- Product
- Sabina I and II EM/EE Patient Lift
- Product code
- FNG Lift, Patient, Ac-Powered
- Reason for recall
- Incorrect length support screws may cause patient lift failure
- FDA root cause
- Other
- Action
- 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.
- Quantity in commerce
- 531 units
- Distribution
- Canada
- Product codes and lots
- Serial Number: Range 401205-41442
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