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Recall Observatory FDA recall evidence

Device product

Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE, Part No. 8128

Z-0560-2019

October 12, 2018

Class II

Product summary

Firm
Atrium Medical Corporation
Event
Event 81524
Status
Terminated
Classification
Class II
Quantity
2930 units
Official record key
device-enforcement:Z-0560-2019

Official wording

Reason: 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.

Code information: ME221275

Distribution pattern: Worldwide distribution - US Nationwide distribution, and country of Saudi Arabia.

Derived failure modes

  • Microbial contamination

    reason.microbial_contamination · v1.0.0

    contamination of the device, the microorganisms
  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    seal defect found in certain sterile