Health product recall

Exoplan

Brand(s)
Last updated

Summary

Product
Exoplan
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
Exoplan Software version 3.1 (Rijeka) 3.1 RIJEKA

Issue

The issue is a software malfunction incorrectly filtering compatibility information contained in the library Straumann® blx/tlx implants and the affected Straumann® step-by-step full drill protocol libraries where multiple sub-full drill protocols exist, e.g., hard-, medium- and soft-bone protocols. The software does not filter out unsupported sleeve height positions for a particular sub-full drill protocol and instead shows all possible sleeve height positions for all sub-full drill protocols.

Recall start date: August 16, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Exocad Gmbh
Rosa-Parks-Str.2, Darmstadt, Germany, 64295
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74222

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