Public recall detail

Exoplan

2023-11-27

medium
Recall Safety notice
Quick summary

Quick summary: Exoplan. Date: 2023-11-27.

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: 2023-11-27.

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-74654

Affected products

ProductExoplan
Lot(01)4260521365019(10)A03B00E** 426052136EXOPLAN21A6 (01)4260521365002(10)A02B03E** (01)4260521365026(10)A03B01E**
Model2.3 MATERA 3.0 GALWAY 3.1 RIJEKA
Serial number(01)4260521365019(10)A03B00E** 426052136EXOPLAN21A6 (01)4260521365002(10)A02B03E** (01)4260521365026(10)A03B01E**
DescriptionExoplan

Issue

During an update of data used in a library shipped with Exoplan or made available on the download portal of Exocad, it was found that the use of a specific combination of an implant, sleeve and surgical drill can result in a hole being drilled 1 mm deeper than expected. Recall start date: October 12, 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-74654
Background{}
CompaniesExocad Gmbh Rosa-Parks-Str.2, Darmstadt, Germany, 64295
AudiencesHealthcare
Source updated2023-11-27

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

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