Medical device recall in Canada: Compress Device surgical technique updated
In plain language
This recall involves several Compress Device components used in surgery, including centering sleeves, anti-rotation spindles, and instrument drills. Zimmer Biomet is updating the surgical technique for these devices. This update ensures correct pin placement and prevents interference during surgery.
What to do
- Healthcare professionals should review the updated surgical technique.
- There is no replacement or modification to the product offered.
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Affected products
Compress Device Centering Sleeve
Model: 178537, 178541, 178542, 178544, 178545, 178738
Lot: 285210, 285220, 609510, 694130, 694150, 784180, 809100, 809130, 830530, 831000
Compress Device Anti-Rotation Spindle
Model: 178350, 178353, 178356
Lot: 046290, 097130, 602000, 921610
Compress Device Anti-Rotation Elliptical Spindle
Model: 178359
Lot: 282760
Compress Instrument Drill for Anti-Rotation Pin
Model: 32-481123
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: 046290, 097130, 602000, 921610, 282760, 285210, 285220, 609510, 694130, 694150, 784180, 809100, 809130, 830530, 831000, All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 178350, 178353, 178356, 178359, 178537, 178541, 178542, 178544, 178545, 178738, 32-481123
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 several Compress Device components used in surgery, including centering sleeves, anti-rotation spindles, and instrument drills. Zimmer Biomet is updating the surgical technique for these devices. This update ensures correct pin placement and prevents interference during surgery.
What should consumers do?
Healthcare professionals should review the updated surgical technique. There is no replacement or modification to the product offered.
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 November 2, 2018.
Is the Compress Device brand affected by this recall?
Yes, Compress Device products are affected by this recall. This recall involves several Compress Device components used in surgery, including centering sleeves, anti-rotation spindles, and instrument drills. Zimmer Biomet is updating the surgical technique for these devices. This update ensures correct pin placement and prevents interference during surgery.