Health product recall

BD Alaris Pump Module Model 8100 (2021-03-03)

Starting date:
March 3, 2021
Posting date:
March 18, 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-75153

Last updated:
2021-03-18

Affected Products 

BD Alaris Pump Module Model 8100

Reason

BD is initiating a new voluntary recall for the BD Alaris Pump Module Model 8100 due to potential lifting of the keypad, which could result in one or more keys becoming unresponsive or stuck (i.E., Constantly pressed state) due to fluid ingress. This issue may potentially result in a delay to the start of infusion or an interruption of infusion.

Affected products

BD Alaris Pump Module Model 8100

Lot or serial number

More than 10 numbers, contact manufacturer. 

Model or catalog number

8100
8100 RECONDITIONED

Companies
Manufacturer

Carefusion 303, Inc.

10020 Pacific Mesa Blvd.

San Diego

92121-2733

California

UNITED STATES