SCFE Knobs recall in Canada: Medical device malfunction risk
In plain language
This recall involves SCFE Knobs, which are part of the Free-Gliding SCFE Screw System, sold in Canada. They are being recalled because vibrations during cleaning may cause screws to loosen, making the knob assemblies dysfunctional. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model and lot numbers.
- Contact Pega Medical Inc. for further instructions.
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Affected products
SCFE Knobs part of the Free-Gliding SCFE Screw System
Model: SCF-KNB265, SCF-KNB273, SCF-KNB365, SCF-KNB373
Lot: 160428-03, 160428-04, 160603-05, 160603-06, A182-05, A182-15, A183-02
Why this matters
Medical device malfunction risk
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: 160428-03, 160428-04, 160603-05, 160603-06, A182-05, A182-15, A183-02
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SCF-KNB265, SCF-KNB273, SCF-KNB365, SCF-KNB373
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?
Medical device malfunction risk
What should consumers do?
Stop using the product immediately. Check the model and lot numbers. Contact Pega Medical Inc. for further instructions.
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?
Yes, there may be a health risk. Medical device malfunction risk
When was this product recalled?
This product was recalled on October 11, 2019.