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Medtronic Xomed, Inc. recalls Lamicel 20PK 5MM INTL
Recalled January 1, 2020 · FDA recall Z-0734-2020 · Medtronic Xomed
Hazard
Routine sterilization dose does not meet the required Sterility Assurance Level. · FDA Class II
Units
307 packs; 6140 units
Sold at
Affected product was only distributed in Japan.
Description
Routine sterilization dose does not meet the required Sterility Assurance Level.
Product
Lamicel 20PK 5MM INTL
Manufacturer(s)
Medtronic Xomed, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →