ARTISET BLOOD TUBING SET (2021-01-05)
- Starting date:
- January 5, 2021
- Posting date:
- January 15, 2021
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-74771
Last updated:
2021-01-15
Affected Products
A. ARTISET BLOOD TUBING SET FOR HAEMODIALYSIS HD SN HC
B. ARTISET BLOOD TUBING SET FOR HAEMODIALYSIS- HD DNL HC
Reason
Baxter Corporation has received customer reports of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments.
Affected products
A. ARTISET BLOOD TUBING SET FOR HAEMODIALYSIS HD SN HC
Lot or serial number
All lots.
Model or catalog number
114533
Companies
- Manufacturer
-
Gambro Dasco S.P.A.
Via Modenese 66
Medolla
41036
ITALY
B. ARTISET BLOOD TUBING SET FOR HAEMODIALYSIS- HD DNL HC
Lot or serial number
All lots.
Model or catalog number
955075
Companies
- Manufacturer
-
Gambro Dasco S.P.A.
Via Modenese 66
Medolla
41036
ITALY