Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE, Part No. 8128
FDA Recall Z-0560-2019 · Posted None
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Recalling FirmAtrium Medical Corporation
Recall StatusTerminated
Product CodeGBZ
Date Initiated2018-10-12
Date Terminated2020-05-12
Product Quantity2930 units
Reason for Recall
This recall has been initiated in response to a seal defect found in certain sterile barrier pouches
containing the device. Affected pouches are un-sealed at the bottom. If the pouch defect is not detected it could represent a serious hazard to the patient.
A sterility breach could potentially lead to product contamination. The potentially affected device is
used in contact with critical anatomical structures and deep into the body. If contaminated, the
consequences for the patient could be severe. The severity of the possible clinical complications
depends on the degree of contamination of the device, the microorganisms involved and the patient s
risk factors. To date, Getinge/Atrium has not received any reports of patient injury related to this
issue.
Firm Action
The firm notified affected customers on October 29, 2018 via an Urgent Medical Device Recall letter. The letter alerted customers to the issue of the product's sterile barrier pouch not being properly sealed at the bottom.
Customers were asked to do the following:
1. Examine your inventory to determine if you have the affected product listed in this
Notification. If so, remove affected products, quarantine them, and place in a secure
location.
2. If you have affected product, contact Atrium Medical Customer Service at 1-800-370-7899,
Monday through Friday between 9:00 am to 5:00 pm (EST), for a Return Authorization (RA) to
return the product for replacement or credit.
3. Complete and sign the enclosed Medical Device - Recall Response Form on Page 4 of this
letter to acknowledge receipt of this notification. If you have affected product to return,
enter the quantity and your RA number in the space provided.
4. Return the completed Medical Device - Recall Response Form to:
EMAIL [email protected] or FAX 1-973-807-1654.
If you have any questions, please contact
your Getinge/Maquet representative or call Maquet Customer Service at 1-603-880-1433, Monday
through Friday between the hours of 9:00 am to 5:00 pm Eastern Time Zone.
Root Cause
Vendor change control
Distribution Pattern
Worldwide distribution - US Nationwide distribution, and country of Saudi Arabia.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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