S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is an optional instrument to add further compression of
FDA device recall Z-1665-2013 · posted 2013-07-05 · Terminated
Recall details
- Recalling firm
- SpineFrontier, Inc.
- Reason for recall
- The outer sleeve would not fit over the S-LIFT Inserter assembly because the hole at the top of the sleeve handle was too small.
- Action taken
- Spine Frontier sent an Urgent Advisory Notice letter dated On June 7, 2013 to all consignees via email. The letter identified the affected product, problem and actions to be taken. The letter informed consignees that a modification has been implemented to the Outer Sleeve component of the S-LIFT Inserter and that SpineFrontier has initiated removal of the affected product from the field.. An acknowledgement form is to be signed and returned from each recipient of the Advisory Notice. Upon receipt of the acknowledgement form and RMA request for part return, replacement parts will be shipped. For questions call 978-232-3990.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- LXH
- Quantity affected
- 12 devices
- Distribution
- USA Nationwide Distribution including the states of: FL, TX, OK, MO, NJ, MA
- Date initiated
- 2013-05-24
- Date posted
- 2013-07-05
- Date terminated
- 2014-10-08
- Location
- Beverly, MA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| S-LIF INTERVERTEBRAL BODY FUSION DEVICE (K092815) | Spinefrontier, Inc. | 2010-06-30 |