Recall MonitorHealth Products
Catalyft™ PL Expandable Interbody System, Interbody Cage
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Orthopaedics
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
Recall class: Type II
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).