Health product recall

SIGMA SPECTRUM Infusion Pump with Master Drug Library (V8 Platform) (2020-09-04)

Starting date:
September 4, 2020
Posting date:
September 25, 2020
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-73983

Last updated: 2020-09-25

Affected Products

SIGMA SPECTRUM Infusion Pump with Master Drug Library (V8 Platform)

Reason

This is a follow-up communication to the urgent Medical Device Safety Alert Baxter previously issued on April 7, 2020, to reinforce important safety information regarding cleaning practices of spectrum infusion pumps. Deviations from the cleaning methods described in the product-specific operator's manual may lead to residue buildup or corrosion of the electrical pins on the pump rear case and battery electrical contacts.

Affected products

SIGMA SPECTRUM Infusion Pump with Master Drug Library (V8 Platform)

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

35700BAX2

Companies
Manufacturer
Baxter Healthcare Corporation
711 Park Ave.
Medina
14103
New York
UNITED STATES