Public recall detail

Ambu Vivasight 2 Dlt Kit

medium
Recall Safety notice
Quick summary

Quick summary: Ambu Vivasight 2 Dlt Kit.

Recommended action

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

Recall details

Quick summary: Ambu Vivasight 2 Dlt Kit.

Official details

Affected product details

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

BrandAmbu A/S
ProductAmbu Vivasight 2 Dlt Kit
IssueMedical devices - Performance
Recall classType II
IdentificationRA-64290

Affected products

ProductAmbu Vivasight 2 Dlt Kit
LotAll lots.
Model412391000 412351000 412411000 412371000
Serial numberAll lots.
DescriptionAmbu Vivasight 2 Dlt Kit

What you should do

  • Confirm receipt of the field safety notice and destroy any remaining units in inventory.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Anaesthesiology
CompaniesAmbu A/S Baltorpbakken 13, Ballerup, Denmark, 2750
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-64290
Background{}
CompaniesAmbu A/S Baltorpbakken 13, Ballerup, Denmark, 2750
AudiencesHealthcare
Source updated2022-06-20

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

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