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Medline Industries Inc recalls Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used in
Recalled January 13, 2021 · FDA recall Z-0782-2021 · Medline Industries
Hazard
The cylindrical sponge component is not x-ray detectable. · FDA Class II
Units
45
Sold at
Foreign distribution only - Canada.
Description
The cylindrical sponge component is not x-ray detectable.
Product
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.
Manufacturer(s)
Medline Industries Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →