Health product recall

BD Alaris Pump Module Model 8100 (2020-08-05)

Starting date:
August 5, 2020
Posting date:
August 28, 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-73789

Last updated: 2020-08-28

Affected Products

BD Alaris Pump Module Model 8100

Reason

Recall is being initiated to notify customers that the BD Alaris Pump Module Model 8100 keypads may exhibit unresponsive or stuck keys as a result of fluid ingress and that 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