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

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  Reason
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  Affected products

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