FDA recall record

Medline Industries Greffe Aorte-LF recall — FDA Z-0782-2021

The cylindrical sponge component is not x-ray detectable.

Class IIclassification
Z-0782-2021official record ID
Jan 13, 2021report date

Recall record at a glance

Official recordZ-0782-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedline Industries Inc.
Report dateJan 13, 2021
Recall initiation dateNov 13, 2020
Quantity45
LocationNorthfield, IL, United States

Official product description

Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Why the product was recalled

The cylindrical sponge component is not x-ray detectable.

Distribution information

Foreign distribution only - Canada.

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: E-Mail.

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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