Recall MonitorHealth Products
Vectorflow Antegrade Catheterization Product
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Gastroenterology and urology
Product: Vectorflow Antegrade Catheterization Product
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: General public, Healthcare, Industry
Recall class: Type II
Products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15232-VF *) |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15232-VFIM |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15232-VFI |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15232-VFM *) |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15552-VFI |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15192-VFIM |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15192-VFM *) |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15422-VFI |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15192-VFI |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15272-VF *) |
| Vectorflow Antegrade Catheterization Product | More than 10 numbers, contact manufacturer. | CS-15312-VFI |
Issue
Teleflex has initiated a voluntary recall for certain lots of the above-mentioned products due to receipt of a supplier-initiated recall of the Merit 16f dual-valved splittable sheath introducer component, which is included in impacted arrow hemodialysis kits and sets. According to the recall notice issued by Merit Medical Systems, Inc.' (Merit), in some cases the sheath introducer may not split as intended due to a design related issue.