Parapost Plus Ti5 (2018-08-09)

Starting date:

August 9, 2018

Posting date:

August 31, 2018

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-67620

• 
  Reason
• 
  Affected products

Affected products

Parapost Plus Ti5

Reason

ParaPost Plus Ti T5 (p/n P2845B), batch number I33012, were packaged with stainless steel posts rather than the titanium post. This incorrect packaging affects only a single batch of product, I33012.

Affected products