Catalyft™ PL Expandable Interbody System, Interbody Cage
Brand(s)
Last updated
Summary
Product
Catalyft™ PL Expandable Interbody System, Interbody Cage
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6069096 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6069113 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6068113 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6069076 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6068076 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6068116 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6068073 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6069116 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6068096 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6069073 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6069093 |
| Catalyft™ PL Expandable Interbody System, Interbody Cage | All lots. | 6068093 |
Issue
This notification is to inform customers of the potential for loss of lordosis and ensure that they are aware of updates that Medtronic is making to the surgical technique and the addition of certain adverse events to the instructions for use (IFU).
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Orthopaedics
Companies
Medtronic Sofamor Danek Usa, Inc.
1800 Pyramid Place, Memphis, Tennessee, United States, 38132
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-78294
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