PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: December 12, 2018 Initiated: October 12, 2018 #Z-0560-2019

Product Description

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

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.

Details

Units Affected
2930 units
Distribution
Worldwide distribution - US Nationwide distribution, and country of Saudi Arabia.
Location
Merrimack, NH

Frequently Asked Questions

What product was recalled?
Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE, Part No. 8128. Recalled by Atrium Medical Corporation. Units affected: 2930 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 12, 2018. Severity: Moderate. Recall number: Z-0560-2019.