FDAOctober 12, 2018device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

atrium medicalatrium

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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