ORBIT INCISOR Plus (2018-02-02)

Starting date:

February 2, 2018

Posting date:

February 16, 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-65982

• 
  Reason
• 
  Affected products

Affected products

ORBIT INCISOR Plus

Reason

Smith & Nephew, Inc. has initiated a field correction for several lots of Orbit Incisor Plus EP-1 due to a manufacturing error. The devices were manufactured with tin-nickel plate as opposed to ep/silver plate.

Affected products