FDA recall record

Covidien Puritan Bennett 560 Ventilator, PB560, CFN 4096600 recall — FDA Z-1775-2022

Medtronic has confirmed six reports from customers outside the US where the ventilator became inoperable due to loss of gas supply caused by manufacturing…

Class IIclassification
Z-1775-2022official record ID
Sep 28, 2022report date

Recall record at a glance

Official recordZ-1775-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCovidien LLC
Report dateSep 28, 2022
Recall initiation dateAug 19, 2022
Quantity5 US
LocationMansfield, MA, United States

Official product description

Puritan Bennett 560 Ventilator, PB560, CFN 4096600

Why the product was recalled

Medtronic has confirmed six reports from customers outside the US where the ventilator became inoperable due to loss of gas supply caused by manufacturing error of specific turbine components.

Distribution information

Domestic distribution to one customer in Washington, D.C. Foreign distribution worldwide.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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