ShockPulse Transducer (2020-05-06)
In plain language
This recall involves the ShockPulse Transducer, a medical device used in Canada. It's being recalled because a component may lose durability, potentially leading to fluid entering the device. Fluid ingress could cause the device to fail or deliver an electrical shock to the user or patient.
What to do
- Stop using the product immediately.
- Check the lot numbers provided in the official notice.
- Follow the instructions from your healthcare provider or the manufacturer regarding return or repair.
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Affected products
ShockPulse Transducer
Model: SPL-T
Lot: 1910PW30607604, 1910PW30607811
Why this matters
Electrical shock or device failure
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: 1910PW30607604, 1910PW30607811
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SPL-T
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?
Electrical shock or device failure
What should consumers do?
Stop using the product immediately. Check the lot numbers provided in the official notice. Follow the instructions from your healthcare provider or the manufacturer regarding return or repair.
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. Electrical shock or device failure
When was this product recalled?
This product was recalled on May 22, 2020.