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Terminated

Zimmer Metasul Head 32/-4'S', taper 12/14, hip implant component; REF 19.32.05.

FDA Recall Z-2299-2008 · Posted 2008-09-17

Recalling FirmZimmer Inc.
Recall StatusTerminated
Product CodeKWA
Date Initiated2008-06-30
Date Terminated2009-01-05
Product Quantity4

Reason for Recall

The wrong part may be in the package. Package may contain a 28 mm head.

Firm Action

Zimmer notified consignees via recall letter dated 6/20/08 to return the product.

Root Cause

Packaging process control

Distribution Pattern

Florida, Pennsylvania, Texas and Virginia.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K033634EPSILON METASUL 32MM ACETABULAR INSERTS, STANDARD AND HOODEDCenterpulse Orthopedics, Inc. · 2004-09-15

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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