Medical device recall in Canada: Compress Device may cause interference
In plain language
This recall involves several Compress Device components, including centering sleeves, spindles, and drills, sold in Canada. They are being recalled because of potential interference between centering sleeves and anti-rotation drills when certain combinations are used. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
Compress Device Centering Sleeve
Model: 178537, 178538, 178541, 178542, 178544, 178545
Lot: More than 10 numbers, contact manufacturer.
Compress Device Anti-Rotation Spindle
Model: 178351, 178352, 178354, 178355, 178357, 178358
Lot: 046290, 097130, 292790, 602000, 921610
Compress Device Anti-Rotation Elliptical Spindle
Model: 178360, 178361
Lot: 282760
Compress Device Short Anti-Rotation Spindle
Model: 178362, 178363, 178364, 178365, 178366, 178367, 178368, 178369, 178370
Lot: 115070
Compress Device Short Anti-Rotation Elliptical Spindle
Model: 178371, 178372, 178373
Lot: All
Compress Instrument Drill for Anti-Rotation Pin
Model: 32-481123
Lot: All
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, 292790, 602000, 921610, 115070, 282760, All, More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 178351, 178352, 178354, 178355, 178357, 178358, 178360, 178361, 178362, 178363, 178364, 178365, 178366, 178367, 178368, 178369, 178370, 178371, 178372, 178373, 178537, 178538, 178541, 178542, 178544, 178545, 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, including centering sleeves, spindles, and drills, sold in Canada. They are being recalled because of potential interference between centering sleeves and anti-rotation drills when certain combinations are used. Stop using the product and follow the return/repair steps in the official notice.
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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 January 9, 2019.
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, including centering sleeves, spindles, and drills, sold in Canada. They are being recalled because of potential interference between centering sleeves and anti-rotation drills when certain combinations are used. Stop using the product and follow the return/repair steps in the official notice.