Product Description
Puritan Bennett 980 Series Ventilator, 980U1ENASAA
Reason for Recall
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
Action Details
On November 4, 2021, the firm began to notify customers through Urgent Medical Device Correction letters. Customers were informed of the device defect that may lead to the ventilator becoming inoperable during use.
Actions you should take
Immediately discontinue use of the affected ventilators. Remove the affected ventilators from clinical service and quarantine the affected ventilators until such time that a Medtronic Technical Service Engineer inspects and replaces the affected printed circuit board assemblies.
Notify all personnel in all care environments in which the affected PB980 series ventilators are used about this medical device correction.
If your facility has distributed affected PB980 series ventilators to other persons or facilities, please promptly forward a copy of this letter to those recipients.
Complete the attached form and return it as directed to confirm your receipt and understanding of this information.
If you are aware of any incidents related to this issue, please contact our Technical Support Department immediately at 1-800-255-6774, option 4, and then option 1 to provide information regarding those events so regulatory reporting obligations can be fulfilled.
Work with the Medtronic Technical Support Department if you require assistance finding alternative ventilation devices.
Beginning November 5, 2021, Medtronic Technical Service will contact all affected customers to schedule a service appointment for all potentially affected ventilators.
If you have any questions regarding this communication, please contact your Medtronic representative or Technical Service at 1-800-255-6774.
Distribution Pattern
Worldwide distribution - US Nationwide.
Code Information / Serial Numbers
GTIN/UDI - 10884521201385
Serial Numbers:
35B1700252
35B1700365
35B1700399
35B1700407
35B1700489
35B1700505
35B1700513
35B1700555
35B1700557
35B1700562
35B1700563
35B1700565
35B1700566
35B1700605
35B1700612
35B1700634
35B1700651
35B1700662
35B1700663
Public Record Disclaimer
This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.