FDA recall record

Zimmer Biomet Biomet DVR Crosslock Screws- 2.7mm x18mm, Sterile ITEM 131827118 Product recall — FDA Z-0709-2019

One lot of product labeled 2.7mm x18mm Lock Screw Square Drive (Lot 029970) contains 20mm locking screws and one lot of product labeled 2.7mm x 20mm Lock…

Class IIclassification
Z-0709-2019official record ID
Jan 16, 2019report date

Recall record at a glance

Official recordZ-0709-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmZimmer Biomet, Inc.
Report dateJan 16, 2019
Recall initiation dateNov 20, 2018
Quantity50 pieces
LocationWarsaw, IN, United States

Official product description

Biomet DVR Crosslock Screws- 2.7mm x18mm, Sterile ITEM 131827118 Product Usage: Usage: The system is intended for stabilization and fixation of small bone fragments in fresh fractures, revision procedures, joint fusion and reconstructions (osteotomies) of small bones of the hand, foot, radius, ulna, ankle, humerus, scapula and pelvis, particularly in osteopenic bone

Why the product was recalled

One lot of product labeled 2.7mm x18mm Lock Screw Square Drive (Lot 029970) contains 20mm locking screws and one lot of product labeled 2.7mm x 20mm Lock Screw Square Drive (Lot 029980) contains 18mm locking screws

Distribution information

Country of Japan

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: Letter.

What to do next

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About this record

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