GE Healthcare medical devices recall in Canada: electrical shock risk
In plain language
This recall involves ComboLab System, CardioLab System, Mac-Lab System, and Mac-Lab Systems - Integrated Electronics Box medical devices sold in Canada. They are being recalled because the power cord may break and expose electrical conductors, posing a shock risk. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and serial numbers.
- Contact GE Healthcare for repair or replacement.
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Affected products
ComboLab System - Main Unit
Model: 2092616-004
Lot: SKP16397103TA
CardioLab System - Main Unit
Model: 2092616-002
Lot: SKP17248451TA, SKP17258483TA, SKP17258484TA
Mac-Lab System - Main Unit
Model: 2092616-001
Lot: SKP17218256TA, SKP17258477TA, SKP17258481TA, SKP17258485TA, SKP17258486TA
Mac-Lab Systems - Integrated Electronics Box
Model: 2098841-001 (2098804-001), P1008CV (2033852-011)
Lot: SG411061097GA, SPH17358709TA, SPH18049347TA
Why this matters
Electrical shock 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: SG411061097GA, SPH17358709TA, SPH18049347TA, SKP16397103TA, SKP17218256TA, SKP17258477TA, SKP17258481TA, SKP17258485TA, SKP17258486TA, SKP17248451TA, SKP17258483TA, SKP17258484TA
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 2092616-001, 2092616-002, 2092616-004, 2098841-001 (2098804-001), P1008CV (2033852-011)
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 risk
What should consumers do?
Stop using the product immediately. Check model and serial numbers. Contact GE Healthcare for repair or replacement.
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 risk
When was this product recalled?
This product was recalled on July 27, 2018.
Is the GE Healthcare brand affected by this recall?
Yes, GE Healthcare products are affected by this recall. This recall involves ComboLab System, CardioLab System, Mac-Lab System, and Mac-Lab Systems - Integrated Electronics Box medical devices sold in Canada. They are being recalled because the power cord may break and expose electrical conductors, posing a shock risk. Stop using the product and follow the return/repair steps in the official notice.