FDA recall record

Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate recall — FDA Z-2744-2015

Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

Class IIclassification
Z-2744-2015official record ID
Sep 16, 2015report date

Recall record at a glance

Official recordZ-2744-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBiomet Spine, LLC
Report dateSep 16, 2015
Recall initiation dateAug 5, 2015
Quantity7 parts
LocationBroomfield, CO, United States

Official product description

Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.

Why the product was recalled

Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

Distribution information

Nationwide Distribution including Distributed nationwide to OH, LA, TX, and GA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: N/A.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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