Public recall detail

Exoplan

2023-09-01

medium
Recall Safety notice
Quick summary

Quick summary: Exoplan. Date: 2023-09-01.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Exoplan. Date: 2023-09-01.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandExocad GmbH
ProductExoplan
IssueMedical devices - Performance
Recall classType II
IdentificationRA-74222

Affected products

ProductExoplan
LotSoftware version 3.1 (Rijeka)
Model3.1 RIJEKA
Serial numberSoftware version 3.1 (Rijeka)
DescriptionExoplan

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesExocad Gmbh Rosa-Parks-Str.2, Darmstadt, Germany, 64295
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-74222
Background{}
CompaniesExocad Gmbh Rosa-Parks-Str.2, Darmstadt, Germany, 64295
AudiencesHealthcare
Source updated2023-09-01

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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