Medline Industries Inc recalls Greffe Aorte-LF (product info is in French); Model DYNJ31877
Recalled 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.
Hazard / Issue
The cylindrical sponge component is not x-ray detectable.
Issued by
FDA
Distribution: Foreign distribution only - Canada.
Lot/Code Info: Lot 20FBW645 (Expiration: 02/28/2022); Lot 20HBM397 (Expiration: 02/28/2022)
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