Health product recall

Acrobat-i Stabilizer Z and Acrobat-i Positioner Z

Last updated

Summary

Product
Acrobat-i Stabilizer Z and Acrobat-i Positioner Z
Issue
Medical devices - Sterility
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Acrobat-i Stabilizer Z

More than 10 numbers, contact manufacturer.

OM-10000Z

Acrobat-i Positioner Z

3000290368
3000353846
3000308238
3000334128
3000355540

XP-5000Z

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Maquet Cardiovascular Llc

45 Barbour Pond Drive, Wayne, New Jersey, United States, 07470

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76418

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