Vectorflow Antegrade Catheterization Product
Last updated
Summary
Product
Vectorflow Antegrade Catheterization Product
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Affected 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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology and urology
Companies
Arrow International Llc Subsidiary Of Teleflex Incorporated
3015 Carrington Mill Blvd., Morrisville, North Carolina, United States, 27560
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Recall date
Identification number
RA-81915
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