Public recall detail

Acrobat-i Stabilizer Z and Acrobat-i Positioner Z

2024-10-31

medium
Recall Safety notice
Quick summary

Quick summary: Acrobat-i Stabilizer Z and Acrobat-i Positioner Z. Date: 2024-10-31.

Recommended action

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

Recall details

Quick summary: Acrobat-i Stabilizer Z and Acrobat-i Positioner Z. Date: 2024-10-31.

Official details

Affected product details

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

BrandMaquet Cardiovascular LLC
ProductAcrobat-i Stabilizer Z and Acrobat-i Positioner Z
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-76418

Affected products

ProductAcrobat-i Stabilizer Z
LotMore than 10 numbers, contact manufacturer.
ModelOM-10000Z
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAcrobat-i Stabilizer Z
ProductAcrobat-i Positioner Z
Lot3000290368 3000353846 3000308238 3000334128 3000355540
ModelXP-5000Z
Serial number3000290368 3000353846 3000308238 3000334128 3000355540
DescriptionAcrobat-i Positioner Z

Issue

The contract manufacturer of the Acrobat product family reported deviations in the manufacturing process that creates the sterile barrier. Specifically, in some instances, the tray sealing step was performed multiple times using the same package, which is outside of the validated process. Although testing suggests that product is sterile immediately after being sealed with this non-validated process, we cannot ensure that the product will remain sterile for the duration of its 2-year shelf life. Recall Start Date: October 21, 2024

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesMaquet Cardiovascular Llc 45 Barbour Pond Drive, Wayne, New Jersey, United States, 07470
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-76418
Background{}
CompaniesMaquet Cardiovascular Llc 45 Barbour Pond Drive, Wayne, New Jersey, United States, 07470
AudiencesHealthcare
Source updated2024-10-31

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

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