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: 2023-09-01
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