Health product recall

CENTRY SYSTEM HEMODIALYSIS BLOOD TUBING SET AND CARTRIDGE (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, Hospitals, Healthcare Professionals
Identification number:
RA-74769



Last updated:
2021-01-15

Affected Products 

A. CENTRY SYSTEM HEMODIALYSIS BLOOD TUBING SET

B. HOSPAL CARTRIDGE WITH HEMOSCAN

C. CARTRIDGE LOW WEIGHT LOW VOLUME

Reason

Baxter Corporation has received customer reports of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments.

Affected products

A. CENTRY SYSTEM HEMODIALYSIS BLOOD TUBING SET

Lot or serial number

All lots.

Model or catalog number

101025

101290

103402

106289

114434

Companies
Manufacturer

Gambro Renal Products S.A. de C.V.

Boulevard Pacifico #10014, Parque Industrial Pacifico,

Tijuana, Baja California N

MEXICO


B. HOSPAL CARTRIDGE WITH HEMOSCAN

Lot or serial number

All lots. 

Model or catalog number

114510

Companies
Manufacturer

Gambro Renal Products S.A. de C.V.

Boulevard Pacifico #10014, Parque Industrial Pacifico,

Tijuana, Baja California N

MEXICO


C. CARTRIDGE LOW WEIGHT LOW VOLUME

Lot or serial number

All lots. 

Model or catalog number

114613

Companies
Manufacturer

Gambro Renal Products S.A. de C.V.

Boulevard Pacifico #10014, Parque Industrial Pacifico,

Tijuana, Baja California N

MEXICO