Cobas e801 Syringes (2018-03-23)

Starting date:

March 23, 2018

Posting date:

April 24, 2018

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-66520

• Reason
• Affected products

Affected products

Cobas e801 Syringes

Reason

The plunger of the Cobas e801 syringe assembly may be mounted in a tilted position which applies mechanical stress to the plunger and may cause r1, r2 or prewash liquids to be pipetted incorrectly.

Affected products