Catalyft™ PL Expandable Interbody System recall in Canada: performance issue
In plain language
This recall involves the Catalyft™ PL Expandable Interbody System, Interbody Cage sold in Canada. It's being recalled because of a potential for loss of lordosis, which is a performance issue. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Catalyft™ PL Expandable Interbody System, Interbody Cage
Model: 6068073, 6068076, 6068093, 6068096, 6068113, 6068116, 6069073, 6069076, 6069093, 6069096, 6069113, 6069116
Lot: All lots
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 6068073, 6068076, 6068093, 6068096, 6068113, 6068116, 6069073, 6069076, 6069093, 6069096, 6069113, 6069116
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
This recall involves the Catalyft™ PL Expandable Interbody System, Interbody Cage sold in Canada. It's being recalled because of a potential for loss of lordosis, which is a performance issue. Healthcare professionals should contact the manufacturer for more information.
What should consumers do?
Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on October 14, 2025.
Is the Medtronic Sofamor Danek Usa, Inc. brand affected by this recall?
Yes, Medtronic Sofamor Danek Usa, Inc. products are affected by this recall. This recall involves the Catalyft™ PL Expandable Interbody System, Interbody Cage sold in Canada. It's being recalled because of a potential for loss of lordosis, which is a performance issue. Healthcare professionals should contact the manufacturer for more information.