Medtronic Xomed, Inc. recalls Lamicel 20PK 5MM INTL
Recalled Product
Lamicel 20PK 5MM INTL
Hazard / Issue
Routine sterilization dose does not meet the required Sterility Assurance Level.
Issued by
FDA
Distribution: Affected product was only distributed in Japan.
Lot/Code Info: UDI: 20885074749055; SPONGE 2203-501EX LAMICEL 20PK 5MM INTL; 2203-501EX; Lots 9642542, 9657414, 9657415, 9657416, 9677915, 9707331, 9707338, 9707334, 9712918
View official government recall
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