Quick summary
Quick summary: Vitek® 2 Ast-N391.
Public recall detail
Vitek® 2 Ast-N391
Recall
Safety notice
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Vitek® 2 Ast-N391.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandBiomerieux, Inc.
ProductVitek® 2 Ast-N391
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-64421
Affected products
ProductVitek® 2 Ast-N391
Lot1411901504 3602133503
Model22233 423341
Serial number1411901504 3602133503
DescriptionVitek® 2 Ast-N391
Issue
Some cartons of the lot of Vitek 2 Ast cards have been identified as impacted by a card and/or card label mix issue during production at the manufacturing site. The card and label of the card are incorrect and are from another Vitek 2 ID or AST reference and lot number. Recall start date: July 25, 2022
What you should do
- Contactez le fabricant si vous avez besoin d'informations supplémentaires.
Additional official information
AudienceHealthcare Industry
CategoryHealth products - Medical devices
CompaniesBiomerieux, Inc. 100 Rodolphe Street, Durham, North Carolina, United States, 27712
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-64421
Background{}
CompaniesBiomerieux, Inc. 100 Rodolphe Street, Durham, North Carolina, United States, 27712
AudiencesHealthcare Industry
Source updated2022-08-02
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
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