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Biomet Spine, LLC recalls Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Recalled September 16, 2015 · FDA recall Z-2744-2015 · Biomet Spine
Hazard
Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440. · FDA Class II
Units
7 parts
Sold at
Nationwide Distribution including Distributed nationwide to OH, LA, TX, and GA.
Description
Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Product
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Manufacturer(s)
Biomet Spine, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →