ENCOR Biopsy Probe (2019-04-24)

Starting date:

April 24, 2019

Posting date:

May 17, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69962

Last updated: 2019-05-17

• Reason
• Affected products

Affected Products

ENCOR Biopsy Probe

Reason

SenoRx Inc. has confirmed that the EnCor Breast Biopsy Probes may be at risk of experience a leak, which could result in minimal suction, leakage, minimal or no tissue sample obtained, or an egress of fluids from the device.

Affected products