medical Class II Updated 2020-01-01

Medtronic Xomed, Inc. recalls Lamicel 10PK 10MM INTL

Recalled Product

Lamicel 10PK 10MM 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: 20613994728917; SPONGE 2205-501EX LAMICEL 10PK 10MM INTL; 2205-501EX; Lots 9767987, 9806170
View official government recall

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